- Research article
- Open Access
- Open Peer Review
Regulation of CNKSR2 protein stability by the HECT E3 ubiquitin ligase Smurf2, and its role in breast cancer progression
BMC Cancer volume 18, Article number: 284 (2018)
Smurf2 E3 ubiquitin ligase physically associates with and regulate the stability of distinct cellular protein substrates. The multi-functional scaffold protein Connector enhancer of kinase suppressor of ras 2 (CNKSR2) plays a key role in regulating cell proliferation, and differentiation through multiple receptor tyrosine kinase pathways. The aim of this study was to investigate whether the interaction between Smurf2 and CNKSR2 has any significant role in the post transcriptional regulation of CNKSR2 expression in breast cancer. Methods: Here we demonstrate a novel interaction of CNKSR2 with Smurf2 by co-immunoprecipitation, indirect immunofluorescence studies, and surface plasmon resonance (SPR) analysis, which can ubiquitinate, but stabilize CNKSR2 by protecting it from proteasome mediated degradation.
CNKSR2 protein levels were significantly increased upon forced overexpression of Smurf2, indicating the role of Smurf2 in regulating the stability of CNKSR2. Conversely, Smurf2 knockdown resulted in a marked decrease in the protein level expression of CNKSR2 by facilitating enhanced polyubiquitination and proteasomal degradation and reduced the proliferation and clonogenic survival of MDA-MB-231 breast cancer cell lines. Tissue microarray data from 84 patients with various stages of mammary carcinoma, including (in order of increasing malignant potential) normal, usual hyperplasia, fibrocystic changes, fibroadenoma, carcinoma-in-situ, and invasive ductal carcinoma showed a statistically significant association between Smurf2 and CNKSR2 expression, which is also well correlated with the ER, PR, and HER2 status of the tissue samples. A comparatively high expression of Smurf2 and CNKSR2 was observed when the expression of ER and PR was low, and HER2 was high. Consistently, both Smurf2 and CNKSR2 showed an integrated expression in MCF10 breast progression model cell lines.
Altogether, our findings reveal that Smurf2 is a novel positive regulator of CNKSR2 and suggest that Smurf2-CNKSR2 interaction may serve as a common strategy to control proliferation of human breast cancer cells by modulating CNKSR2 protein stability.
The ubiquitin-proteasome system (UPS) plays a prominent role in cell regulatory mechanism to maintain homeostasis. Evidently, every part of the cell is under the control of the ubiquitin-proteasome regulatory system. The peptide products of this proteasome system provides additional outcome by functioning as a critical factor in deciding whether a cell will be recognized as infected or tumorigenic by the immune system and destroyed, or recognized as self and spared . In many cases, stability of several important scaffold proteins is controlled by ubiquitination, a predominant posttranslational modification central to eukaryotic regulation [2, 3]. E3s carry out the key rate-limiting step in ubiquitin-mediated proteolysis. Multiple E3 ubiquitin ligases can targets same protein and vice versa, corroborating a highly complex and dynamic regulation . Hence, the dynamic role of cellular ubiquitination can be further confirmed by identifying new targets for a given ubiquitin ligase and, conversely, new ubiquitin ligases for a given target .
Smurf2 is a C2-WW-HECT E3 ubiquitin ligase that has the ability to ubiquitinate and degrade some proteins, e.g., the TGF-β receptor I and associated Smad proteins involved in TGF- β/BMP signaling, but also have a unique ability to protect other substrates, e.g., spindle assembly checkpoint protein, MAD2 and NEDD9/HEF1 . It contains WW domains, which directly bind to a PPXY motif (also known as PY motif) in its targets which is further stabilized by the PY tail, a six-amino acid stretch immediately carboxylterminal to the PPXY motif, although additional interactions exist . Smurfs are frequently deregulated in human cancers and are critical regulators of multiple oncogenic factors. However, the specific role of Smurf2 in tumorigenesis has been highly obscure, with numerous studies showing that it is either pro-tumorigenic or, conversely, anti-tumorigenic in a context-dependent manner. Smurf2 has involved in diverse signal pathways and cellular processes by targeting broad spectrum of proteins. Recent studies emphasize the growing appreciation that the pleiotropic effects of Smurf2 might be explained by the ability of Smurf2 to target potential molecular substrates in a ligase dependent and independent manner. Thus, expanding the family of Smurf2 targets may provide further insights into regulatory role of Smurf E3 ubiquitin ligases in the cellular environment .
CNK (Connector enhancer of kinase suppressor of ras) is a putative multi-adaptor scaffold protein required in multiple receptor tyrosine kinase pathways particularly in RAS-RAF/ mitogen–activated protein kinase (MAPK) cascade which is involved in conveying several proliferative and differentiative signals to the nucleus . CNKSR2 (Connector enhancer of kinase suppressor of ras 2) also named as Membrane-Associated GUanylate kinase Interacting protein (MAGUIN) is a mammalian isoform of CNK, and is the closest homolog to Drosophila melanogaster and C. elegans CNK, thus likely represents the orthologous member. The neuronal isoform CNK2 has an essential function in nerve growth factor-induced, sustained stimulation of ERK leading to neuronal differentiation . But CNK2 is not required for epidermal growth factor-dependent, transient stimulation of ERK occurring during cell proliferation. CNK’s multidomain architecture suggests that it has the ability to bind and bring together different molecules as previously shown for several other multidomain molecules . In particular, consistent with other known potential substrates of Smurf2, we have also identified a probable Smurf2-interacting motif in CNKSR2, a ‘SPPPPY’ motif at 702–707 sequence region that shows a strong PY motif match with Smurf2. Indeed, we observed that knockdown of Smurf2 downregulated the expression of CNKSR2 and reduced the proliferative potential of human breast cancer cells . Hence we hypothesized that CNKSR2 may be a novel substrate for Smurf2 E3 ubiquitin ligase which seems to perform a crucial role in regulating the stability of CNKSR2. However, whether additional ubiquitin ligases for CNKSR2 exist and how CNKSR2 is regulated by various ubiquitin ligases are not clearly defined.
Plasmids, cell lines and culture conditions
pCMV5B-Flag-Smurf2 and pCMV5B-Flag-Smurf2 C716A plasmids have been described  and were purchased from Addgene, Cambridge, MA, USA. Human embryonic kidney 293 (HEK293) cells were purchased from National Centre for Cell Science (NCCS, Pune, India). Immortalized normal human breast epithelial cell line MCF10A, and the human breast cancer MCF-7 and MDA-MB-231 cells were purchased from the American Type Culture Collection (ATCC; Manassas, VA, USA). The pre-malignant and in situ grade cell lines-MCF10AT and MCFDCIS were a kind gift from Dr. Suresh Kumar Rayala (Indian Institute of Technology-Madras, India). MCF10A and MCF10AT cells were cultured in Dulbecco’s modified eagles medium (DMEM)/Nutrient F12-Ham (1:1) supplemented with 10% fetal bovine serum (FBS), 20 ng/ml Epidermal Growth Factor (EGF), 100 ng/ml cholera toxin, 0.01 mg/ml Insulin-Transferrin-Selenium (ITS), 500 ng/ml hydrocortisone, and 1 ng/ml Fibroblast Growth Factor (FGF). MCFDCIS, MCF-7 and MDA-MB-231 cells were grown at 37 °C with 5% CO2 in Dulbecco’s modified eagles medium (DMEM) medium supplemented with 10% FBS and 1% penicillin/streptomycin (Invitrogen; Carlsband, CA, USA).
Human breast tissue samples were collected from Regional Cancer Centre (RCC), Thiruvananthapuram, India after obtaining approval from the Institutional Human Ethics Committee. The samples were collected from patients who underwent primary surgery without prior chemotherapy or radiotherapy. Informed consent was taken from all the patients prior surgery/excision of tissue.
siRNA and shRNA transfections
siRNA against Smurf2, in the form of either a mixture of three siRNAs targeting different regions of Smurf2 (Santa Cruz Biotechnology; Texas, USA), or the negative control siRNA included in the kit (Santa Cruz Biotechnology; Texas, USA) was transfected into 60–70% confluent MDA-MB-231 cells with siLentFect (Bio-Rad; CA, USA) according to the manufacturer’s instructions. Three days later, cells were subjected to western blotting, immunoprecipitation, and quantitative RT-PCR analysis.
Stable knockdown of Smurf2 in MDA-MB-231 cells was achieved by transfecting Smurf2 shRNA plasmid containing a pool of three target-specific lentiviral vector plasmids each encoding 19–25 nucleotide (plus hairpin) shRNAs designed to knockdown Smurf2 gene expression (Santa cruz biotechnology; Texas, USA) using Amaxa® Cell Line Nucleofector® Kit V (Lonza; Basel, Switzerland) according to the manufacturer’s instructions. Briefly, 1 × 106 cells were transfected with 2 μg plasmid DNA in 100 μl cell Line Nucleofector® Solution V (Lonza; Basel, Switzerland) and seeded in 6-well plate containing pre-equilibrated DMEM medium. After 24 h, cells were selected for stable integration using 1 μg/ml Puromycin (Sigma; St. Louis, MO, USA) for 3 weeks and were used for further experiments. MDA-MB-231 cells stably expressing Control shRNA Plasmid-A (Santa Cruz Biotechnology; Texas, USA) were also generated in the same fashion to serve as negative control.
For cultured cells, in a 10-cm dish format, HEK293 cells transfected with empty vector, pCMV5B-Flag-Smurf2 WT, or pCMV5B-Flag-Smurf2 C716A were washed in 1 × PBS and resuspended in 1 ml of lysis buffer (70 mM NaCl, 50 mM Tris, pH 8 and 0.5% NP-40), supplemented with phosphatase inhibitor and protease inhibitor cocktails (Sigma; St. Louis, MO, USA). After rotating at 4 °C for 30 min, the cell lysate was collected and precleared by spinning at 14,000 rpm for 10 min. For co-immunoprecipitation of endogenous Smurf2 with CNKSR2, total protein was isolated from MDA-MB-231 as described previously. For each pull down, 3 μg of corresponding antibody was added to the normalized lysate (1 mg of total protein by Bradford’s Assay, Bio- Rad; CA, USA)) and the mixture was incubated overnight at 4 °C. Normal rabbit IgG was used as negative control. Immune complexes were then precipitated with protein A sepharose macrobeads (Sigma; St. Louis, MO, USA). Beads were washed four times with lysis buffer and immunoprecipitated samples were resolved by SDS-PAGE for immunoblotting.
Surface plasmon resonance (SPR)
Binding kinetics was determined by SPR using a ProteOn XPR36™ SPR instrument (Bio-Rad; CA, USA) with a GLC (General Layer Compact) biosensor chip (Bio-Rad; CA, USA) with its unique “one-shot” kinetics approach. The apparatus has six parallel flow channels for uniformly immobilizing strips of six ligands on the sensor surface. The fluidic system can be rotated automatically to 90° so that up to six different analytes can be injected, thereby simultaneously monitoring up to 36 individual molecular interactions in a single run on a single chip . In our study, the ligand (recombinant Smurf2 protein; Sigma; St. Louis, MO, USA) was immobilised to the biosensor surface layer by amine coupling chemistry, followed by capture of the analyte (recombinant CNKRS2 protein; Cusabio Biotech, China) as described previously (Bravman et al., ). One of the six ligand channel (L4) was used to capture the Smurf2 protein and one ligand channel was left blank (L6) by injecting the 10 mM sodium acetate buffer, pH 4.0 (without Smurf2), which served as the ligand reference channel. The chip surface was activated for the two ligand channels (L4 and L6) using a mixture of 5 mM N-hydroxysulfosuccinimide (sulfo-NHS) and 20 mM 1-ethyl-3(3-dimethylaminopropyl)-carbodiimide (EDC), ethanolamine-HCl) mixed in 1:1 ratio to maintain a uniform composition throughout the chip. This was followed by an immediate injection of 300 μl of 7.5 μg/ml of the recombinant Smurf2 protein in 10 mM sodium acetate buffer, pH 4.0 for 600 s. Immobilisation was performed at 25 °C at a flow rate of 30 μl/min using PBS/Tween (Phosphate buffered saline, pH 7.4, 0.005% Tween 20), as the running buffer. The sensor chip surface was then inactivated using 120 μl of 1 M ethanolamine-HCl to block residual NHS-activated carboxyl groups on the chip surface. The final immobilization levels of the Smurf2 ligand was ~ 2000 response units (RU) (1 RU = 1 pg of protein/mm2).
During the interaction step the running buffer used was 20 mM Tris-HCl, pH -8.0, 0.5 M NaCl. The system was primed with the running buffer before the start of the experiment. Four of the six analyte channels (A1-A4) were used to capture CNKRS2 at four different concentrations using a twofold dilution series ranging from 0.25 μM to 2 μM. All the four different analyte concentrations were passed simultaneously (a single injection) in the analyte direction at a flow rate of 100 μl/min for 60 s of association with Smurf2, followed by dissociation for 600 s. In the sixth channel (A6), ‘analyte running buffer’ without any protein was injected for double referencing. All these assays were done at 25 °C. All binding sensorgrams were collected, processed, and analyzed using the integrated ProteOn Manager software version 188.8.131.52 (Bio-Rad; CA, USA). Response data from the ProteOn instrument were normalized to a baseline value of zero just prior to the start of the analyte injection. Responses from the reference positions before and after each reaction spot were corrected by subtracting the non-specific response observed in the reference surface to remove non-specific binding and the large step changes in response due to changes in buffer refractive index (‘buffer shift’). Finally, the binding curves were grouped fitted using the Langmuir model describing 1:1 binding stoichiometry with one local parameter for surface capacity (Rmax), one association rate constant (ka or kon), and one dissociation rate constant (kd or koff). The ratio of the rate constants (kd/ka) yielded the value for the equilibrium or affinity constant (KD).
HEK293 cells were transfected with pCMV5B-Flag-Smurf2 WT, fixed with ice-cold acetone/methanol (1:1) and blocked with 3% BSA in PBS for 1 h at room temperature. Cells were then incubated with mouse Flag (Sigma; St. Louis, MO, USA) and rabbit CNKSR2 (Abcam; Cambridge, UK) antibodies, followed by incubation with FITC-conjugated anti-mouse and PE-conjugated anti-rabbit (Santa cruz Biotechnology; Texas, USA) secondary antibodies. For immunofluorescence of endogenous Smurf2 and CNKSR2, cells were fixed with ice-cold acetone/methanol (1:1) and blocked with 3% BSA in PBS for 1 h at room temperature. Cells were then incubated with goat Smurf2 (Santa Cruz Biotechnology; Texas, USA) and rabbit CNKSR2 (Abcam; Cambridge, UK) antibodies, followed by incubation with FITC-conjugated anti-goat and PE-conjugated anti-rabbit (Santa Cruz Biotechnology; Texas, USA) secondary antibodies. Cells were also stained with Propidium Iodide (PI) and Hoecht dye to reveal nuclei. Immunofluorescence was monitored by both conventional and confocal microscopy.
For ubiquitination of endogenous CNKSR2 after Smurf2 overexpression, HEK293 cells were transfected with Smurf2WT, Smurf2C716A, and empty vector and disrupted in IP lysis buffer (70 mM NaCl, 50 mM Tris, pH 8, 0.5% NP-40) supplemented with 1 × phosphatase inhibitor and 1 × protease inhibitor cocktails (Sigma; St. Louis, MO, USA). Lysates were denatured by boiling for 15 min and diluted 10-fold in IP buffer (70 mM NaCl, 50 mM Tris, pH 8, 0.5% NP-40) supplemented with 1 × phosphatase inhibitor and 1 × protease inhibitor cocktails (Sigma; St. Louis, MO, USA). The lysates were immunoprecipitated with rabbit CNKSR2 (Abcam; Cambridge, UK) followed by incubation with protein A sepharose macrobeads (Sigma; St. Louis, MO, USA). Ubiquitinated CNKSR2 was revealed by mouse ubiquitin (Santa Cruz Biotechnology; Texas, USA) immunoblotting. 1% total cell lysate was also included as Input control.
For ubiquitination of endogenous CNKSR2 after Smurf2 knockdown, MDA-MB-231 cells were seeded at 2 × 105 cells/well in 6-well format and treated with Control siRNA or Smurf2-specific siRNA. Cells were treated for 4 h with 10 μM MG132 (Calbiochem; CA, USA) 44 h post-transfection, and disrupted in the lysis buffer (70 mM NaCl, 50 mM Tris, pH 8 and 0.5% NP-40). Lysates were denatured by boiling for 15 min and diluted 10-fold in IP buffer (70 mM NaCl, 50 mM Tris, pH 8, 0.5% NP-40 1Xprotease inhibitor, 1XSer/Thr and Tyr phosphatase inhibitor). The lysates were immunoprecipitated with either control rabbit IgG (Santa cruz biotechnology; Texas, USA), or rabbit CNKSR2 (Abcam; Cambridge, UK). Entire immunoprecipitates were loaded onto gel; gel was transferred onto PVDF membrane as usual. Ubiquitinated CNKSR2 was revealed by mouse ubiquitin (Santa Cruz Biotechnology; Texas, USA) immunoblotting. 1% total cell lysate was also included as Input control.
Breast cancer tissue arrays with progressive changes- BRC961 and BRC962, non-overlapping with each other and each containing 48 cases from normal, premalignant and cancer tissues with progressive grades and stages in duplicates were purchased from Pantomics. Expression of Smurf2 and CNKSR2 was evaluated using an indirect immunoperoxidase procedure (ABC-Elite, Vector Laboratories; CA, USA). Briefly, TMA slides were baked at 60 °C for 30 min before use. The slides were then deparaffinized in xylene and rehydrated in graded ethanol/isopropanol. Endogenous peroxidase activity was blocked by incubating the slides in 1.5% H2O2 in methanol for 20 min at room temperature. Antigen retrieval was done by dipping the slides for 12 min in boiling citrate buffer. The slides were then blocked with 3% BSA-PBS for 1 h at room temperature. After blocking, the sections were incubated with primary antibodies; rabbit Smurf2 (Santa cruz Biotechnology; Texas, USA) and rabbit CNKSR2 (Abcam; Cambridge, UK), in 1% BSA-PBS at 4 °C overnight. Bound antibody was detected using Vectastain ABC kit (ABC-Elite, Vector Laboratories; CA, USA). Briefly, post PBS wash, the sections were incubated with universal biotinylated anti-mouse IgG/rabbit IgG secondary antibody (C) in normal horse serum blocker (supplied in the kit) for 30 min at room temperature. The sections were then washed thrice in 1XPBS followed by incubation with A + B mixture (Avidin+Biotinylated Horseradish Peroxidase) for another half an hour at room temperature. The sections were again washed with 1XPBS and incubated in DAB (Sigma; St. Louis, MO, USA) solution till they developed brown color. Further, the sections were washed in distilled water and counterstained with hematoxylin for 1 min for nuclear staining. The sections, after bluing for 10 min under running tap water were dehydrated in graded ethanol changes and finally, cleared in xylene. The sections were then mounted using DPX (Qualigens; India) and visualized using a digital up-right microscope, Leica DMI 1000, at 40× magnification.
For scoring, at least five randomly selected high power fields were chosen and a total number of 1000 cells were considered. Only epithelial cells were evaluated. The cells were considered nuclear positive if the nuclei stained positive irrespective of the intensity of staining. Cytoplasmic positivity of Smurf2 and CNKSR2 were measured depending on the intensity of immunoreactivity and scored as mild (+), moderate (++), and intense (+++). The staining intensity in each core biopsy was recorded separately. Slides were read blinded by two readers (D.D. and A.N.) along with discussions made with an expert pathologist. The IHC data regarding ER, PR, and HER2 staining intensity of the corresponding tissues were obtained from Pantomics.
Quantitative real time PCR
shRNAs against Smurf2 (Santa Cruz Biotechnology; Texas, USA) or the negative control shRNA (Santa cruz biotechnology; Texas, USA) was transfected into MDA-MB-231 cells using Amaxa® Cell Line Nucleofector® Kit V (Lonza; Basel, Switzerland) according to the manufacturer’s instructions. Cells were selected for stable integration using 1 μg/ml Puromycin (Sigma; St. Louis, MO, USA) for 3 weeks and total RNA was isolated with TRIzol (Ambion/Invitrogen; Carlsband, CA, USA), and quantitative real-time RT-PCR was performed in three triplicates with primer sets specific for Smurf2(forward,TGGATCAGGAAGTCGGAAAA and reverse, GGACATGTCTAACCCCGGA) and CNKSR2 (forward, CGACCTCCCTCGATGAGTTG and reverse, CACTGCACTGCTCCCAGTTA) and the control gene GAPDH (forward, TTGGTATCGTGGAAGGACTCA and reverse, TGTCATCATATTTGGCAGGTT). Products were amplified and detected with the Power SYBR Green PCR Master Mix (Applied Biosystems; Massachusetts, USA) on an.
ABI 7900HT Fast Real-Time PCR System (Applied Biosystems; Massachusetts, USA) according to the manufacturer’s instructions. The real time analyses were done by 2-ΔΔCt method  using SDS 2.1 software (Applied Biosystems; Massachusetts, USA) after normalization with the GAPDH control.
Clonogenic assay or foci formation assay was performed as described previously . Briefly, cells were seeded at a density of 500 cells/well in six-well plates and incubated for 14 days with intermittent media change at every 2 days. After 14 days, plates were rinsed carefully twice with 1 × PBS and fixed with 4% paraformaldehyde. After fixation, cells were washed thrice with 1 × PBS and stained with 0.5% crystal violet for 30 min at room temperature on a rocking platform. The dishes were rinsed three times with water, air-dried and analyzed. Colonies comprising more than 50 cells were counted manually and images were obtained using a digital camera. The experiments were done in duplicate at least three times.
Soft agar colony assay
Anchorage-independent growth was determined by soft agar analysis as follows: Smurf2 knockdown MDA-MB-231 cells were trypsinized and 1 × 104 cells per 35-mm dish were seeded in 0.35% agar on top of a base layer containing 0.8% agar. Plates were incubated at 37 °C at 5% CO2 in a humidified incubator for 21 days. After 21 days, the colonies were fixed with 4% paraformaldehyde and stained with 0.05% crystal violet for 1 h. Colonies with > 50 cells were counted under a microscopic field at 10× magnifications. The experiments were done in duplicates at least three times.
Statistical analysis was performed using Intercooled Stata software (Intercooled Stata 11.2 version). The expression of Smurf2, CNKSR2, ER, PR, and HER2 were compared between tumor grades using Chi squared test. The effects of Smurf2 and CNKSR2 expression on histopathological grade of the tumor were estimated with Odds Ratio (OR) (unadjusted Odds ratio) and their 95% Confidence Interval (CI) derived from binary logistic regression model. In order to assess the independent effect of Smurf2, CNKSR2, ER, PR, and HER2 expression on tumor grade, we included all the five factors in the multiple logistic regression model and estimated the Odds Ratio (OR) (adjusted Odds ratio) and their 95% Confidence Interval (CI). All data were obtained by at least three independent experiments and represented as mean ± standard deviation. The limit of statistical significance was set at P < 0.05.
CNKSR2 is a novel interacting protein of Smurf2
Our previous findings that CNKSR2 encompasses a ‘SPPPPY’ motif at 702–707 amino acid sequence region that forms an energy stable complex with Smurf2 WW2 domain in silico, and the decreased expression of CNKSR2 following Smurf2 knockdown , prompted us to examine whether there were direct physical and molecular interactions between Smurf2 and CNKSR2. To determine whether endogenous Smurf2 and CNKSR2 interact with each other, we performed co-immunoprecipitation of Smurf2 with CNKSR2 from cell lysates isolated from MDA-MB-231 cells. Indeed, Smurf2 was readily detected in CNKSR2 immunoprecipitates (Fig. 1a) and reciprocally, CNKSR2 was found in Smurf2 immunoprecipitates (Fig. 1b). This interaction is specific for Smurf2, as the interaction of endogenous Smurf1 with CNKSR2 was not detected (Fig. 1a). Thus, CNKSR2 specifically interacts with Smurf2. Our observations do not exclude the possibility that this interaction could require other proteins, but these data do suggest that Smurf2 and CNKSR2 are in complex with each other.
Smurf2 interacts with CNKSR2 in a ligase independent manner
To confirm that endogenous CNKSR2 associates with Smurf2 and to analyse if forced overexpression of Smurf2 increased CNKSR2 levels, HEK293 cells were transfected with Flag-tagged Smurf2 WT, Flag-tagged Smurf2 C716A, and empty vector followed by immunoprecipitation and immunoblotting. CNKSR2 was identified only in Smurf2-expressing cells (Fig. 2a), and the levels of CNKSR2 were substantially increased by transfection with Flag-tagged Smurf2 WT, compared with control plasmid (Fig. 2b). As Smurf2 is an E3 ubiquitin ligase, we next asked if the Smurf2 enzymatic activity was required for it to interact with CNKSR2. Interestingly, expression of a catalytically inactive Smurf2 mutant (C716A, targeting the HECT domain) also upregulated the levels of CNKSR2 (Fig. 2a, b). These results provide support for the idea that Smurf2 positively regulates CNKSR2, and the Smurf2-CNKSR2 interaction is also independent of the enzymatic activity of Smurf2.
Even though CNKSR2 was found to interact with both wild type and ligase deficient mutant Smurf2, the expression level of CNKSR2 was significantly high in Smurf2 WT transfected cells compared with Smurf2 C716A transfected cells, which prompted us to investigate the ubiquitination status of CNKSR2 following interaction with Smurf2. Hence we immunoprecipitated CNKSR2 from HEK293 cells transfected with either catalytically active wild-type (WT) or a catalytically dead C716A mutant of Smurf2 and immunoblot analysis was performed using mouse ubiquitin antibody. As shown in Fig. 2c, Smurf2 WT moderately increased the ubiquitination of CNKSR2, whereas Smurf2 (C716A) mutant had no effect, indicating that Smurf2 has some role in regulating the ubiquitination of CNKSR2. Altogether, these data indicate that Smurf2 can interact with CNKSR2 leading to its ubiquitination; however, Smurf2-dependent ubiquitination is protective for CNKSR2, which was further supported by an increased expression of CNKSR2 in Smurf2 WT transfected cells compared with Smurf2C716A transfected cells as shown in Fig. 2b.
CNKSR2 co-localizes with Smurf2
Consistent with the interaction between Smurf2 and CNKSR2, the two proteins co-localize particularly in the cytoplasm. After HEK293 cells were transfected with Flag-Smurf2, indirect immunofluorescence demonstrated that both CNKSR2 and Smurf2 were primarily co-localized to the cytoplasm (Fig. 3a, b). Endogenous CNKSR2 and Smurf2 also co-localized primarily in the cytoplasm of MDA-MB-231 cells (Fig. 3c, d), and the co-localization was especially visible under higher magnification and better resolution. Combining the results of all the experiments, CNKSR2 apparently interacts with Smurf2 in mammalian cells.
Binding kinetics of Smurf2 and CNKSR2
Capture of Smurf2
Figure 4 gives the SPR responses obtained from channel L4 during Smurf2 immobilization (7.5 μg/ml). Channel L6 was used only as a reference channel, to offset buffer shift and subtract non-specific interactions of the analyte with the chip surface from SPR responses in the Smurf2 channel. In practice, a reference channel need not be immobilized with protein but can simply be NHS-activated and then blocked with ethanolamine to remove (negatively charged) carboxyl groups and reduce electrostatic interactions. Following immobilization, 1 M ethanolamine-HCl was used to deactivate the ligand channel and to block residual NHS-activated carboxyl groups, to remove loosely bound Smurf2 molecules and ensure a uniform baseline. A stable baseline response of ~ 2000 RU was obtained in channel L4 following Smurf2 capture, so there was no drift in SPR response that would affect the apparent kinetics during CNKSR2 interaction analysis.
CNKSR2-Smurf2 interactions- one-shot kinetics approach
The changes in refractive index occurred during the direct interaction between two proteins could be analysed by a novel method called Surface plasmon resonance (SPR). The ligand protein is immobilised on a sensor chip via covalent coupling. The analyte is injected over the chip surface and any binding between the two which results in a change in surface mass is recorded and measured as a change in refractive index. In the present study, we have examined the potential interaction between Smurf2 and CNKSR2. A unique feature of the ProteOn XPR36 system is its ability to collect kinetic data for all the four different analyte concentrations over the target ligand surface at one time.
Sensorgrams showing the raw and processed data (after subtraction of L6 responses) following the injection of the analyte CNKSR2 (injected for 60 s over the ligand surface) at four different concentrations from 0.25 μM, 0.5 μM, 1 μM, and 2 μM, in a two fold dilution series, immediately after the capture of Smurf2 are shown in Fig. 5a, b. The data from the reference spots were used to correct any baseline drift due to bulk refractive index change and non-specific bindings. The sensorgrams in the ligand channel overlap at each analyte concentration, showing good reproducibility.
The SPR responses obtained from the interaction between different concentrations of CNKSR2 and Smurf2 were fitted using the Langmuir 1:1 bimolecular interaction model, according to the equation given below, using ProteOn Manager software version 184.108.40.206 (Bio-Rad, USA).
Figure 6 shows the curve fits and the kinetic constants for the fits including single grouped ka (association rate constant), kd (dissociation rate constant), KD (equilibrium or binding affinity constant) and Rmax were obtained using the Langmuir model and are reported in Table 1. For the interaction surface, the modelled data overlay the experimental data, indicating that these binding events are well described by a simple interaction model.
The results from the Smurf2-CNKSR2 interaction seem to fit well using the Langmuir model in which one ligand molecule interacts with one analyte molecule. An equilibrium dissociation constant (KD) of 13.9 nM was calculated from the ratio of the association and dissociation rates indicating a stable interaction between Smurf2 and CNKSR2.
Depletion of Smurf2 decreased CNKSR2 protein stability with enhanced ubiquitination
We reported previously that Smurf2 knockdown significantly downregulated the CNKSR2 protein levels in MDA-MB-231, MCF-7, SW480, and SCC131 cancer cell lines without any effect on CNKSR2 mRNA, suggesting that Smurf2 controls the CNKSR2 protein level possibly through proteolytic regulation. Likewise, a comparatively rapid degradation of CNKSR2 was observed in Smurf2 depleted cells following cycloheximide chase assay, implying the potential role of Smurf2 in regulating the stability of CNKSR2 protein . Lending further support that Smurf2 modulates CNKSR2 expression, we analyzed the role of proteasome mediated degradation in maintaining the stability of CNKSR2 using the proteasome inhibitor, MG132. Our experiments showed increase in CNKSR2 expression following MG132 treatment. Concomitantly, the expression of Smurf2 was also found to be upregulated following MG132 treatment (Fig. 7a). Further we examined whether Smurf2 depletion accelerates the proteasome mediated degradation of CNKSR2. As we expected, treatment with MG132 substantially rescued the down-regulation of CNKSR2 in Smurf2 depleted cells (Fig. 7b). Correspondingly, to analyze whether the proteasome mediated degradation of CNKSR2 was dependent on polyubiquitination, CNKSR2 was immunoprecipitated from Smurf2-depleted MDA-MB-231 cells treated with MG132, and then analyzed by immunoblotting with mouse ubiquitin antibody (Fig. 7c). Polyubiquitination of CNKSR2 was significantly enhanced in cells treated with Smurf2 siRNA and MG132, compared with cells treated with non-specific siRNAs and MG132. Our results therefore suggest that depletion of Smurf2 leads to enhanced polyubiquitination and subsequent degradation of CNKSR2.
Smurf2 and CNKSR2 exhibit coordinated expression in human breast cancer progression model cell lines
Since the expression of Smurf2 was found to be elevated in human breast cancer cell lines and is involved in the proliferation and migration of breast cancer cells via interaction with CNKSR2, we investigated its role in the advancement of breast cancer by examining the expression along with CNKSR2 in an in vitro breast cancer progression model comprising MCF10A, MCF10AT, MCFDCIS, MCF-7 and MDA-MB-231. This series of cell lines provides a unique opportunity to study breast cancer progression, induced in a defined method, in a common cell background. Interestingly, we observed that both Smurf2 and CNKSR2 displayed a comparatively similar pattern of expression in mammary cells with increasing tumorigenic potential. Together Smurf2 and CNKSR2 was found to be significantly upregulated in MDA-MB-231 cells, even though a moderately high expression was also observed in MCFDCIS and MCF-7 cells compared to the normal (MCF10A) and premalignant (MCF10AT) cell lines (Fig. 8a).
Furthermore, subcellular localization of Smurf2 and CNKSR2 in breast progression model cells (Fig. 8b, c) also exhibited an analogous expression consistent with the western blot results showing progressively elevated expression with increasing tumorigenic potential. In normal and pre-maligant cells, Smurf2 and CNKSR2 were found to have a very low expression and are localized mainly in the nucleus. However, in MCFDCIS and MCF-7 we observed a more intense expression of Smurf2 and CNKSR2 in both the nucleus and cytoplasm. Alternatively, in MDA-MB-231 cells, both Smurf2 and CNKSR2 showed a significantly high expression localized mainly in the cytoplasm. Only a very mild expression of Smurf2 and CNKSR2 was observed in the nucleus.
Expression of Smurf2 and CNKSR2 is dysregulated in human breast tissues
Recent reports by Jin et al., 2009 highlighted the importance of Smurf2 proteins in breast cancer ; therefore to study the functional role of Smurf2 and CNKSR2 in human breast cancer tissues, we initially analyzed the expression levels of Smurf2 and CNKSR2 proteins in eight matched-sets of primary mammary carcinoma (Invasive Ductal Carcinoma, IDC) and adjacent normal breast tissue samples by western blotting. As shown in Fig. 9a, 87.5% of mammary carcinoma had elevated expression of Smurf2 compared to their normal counterparts. Similarly, CNKSR2 was also found to be overexpressed in 62.5% of malignant breast tumors compared to the adjacent normal breast tissues. We further analyzed the mRNA levels of Smurf2 and CNKSR2 in human breast cancer tissue samples (n = 8 for IDC) and adjacent normal breast tissue (n = 6 for normal) by real time quantitative PCR and observed approximately three fold upregulation in the expression of Smurf2 in invasive mammary carcinoma compared to non-tumor tissues (Fig. 9b). However, CNKSR2 does not exhibit a significant upregulation at the mRNA level in breast tumor samples compared to normal breast tissues (Fig. 9b), which indicate that expression status of Smurf2 and CNKSR2 is mainly associated at the protein level rather than at the mRNA level.
Smurf2 and CNKSR2 expression is associated with progressive changes in breast cancer
Notably high expression of Smurf2 in human breast cancer tissues and cell lines and its harmonized expression with CNKSR2 in breast cancer progression model cell lines prompted us to investigate the expression status of Smurf2 and CNKSR2 in human breast cancer subtypes by analyzing tissues from various stages of mammary carcinoma, including (in order of increasing malignant potential) normal, usual hyperplasia, fibrocystic changes, fibroadenoma, carcinoma-in-situ, and invasive ductal carcinoma (Fig. 10), thereby to explore the possible association between Smurf2 and CNKSR2 in progression of breast cancer and to translate our in vitro findings. The TMA included 8 cases of normal/hyperplasia, 7 cases each of fibrocystic changes, fibroadenoma, and ductal carcinoma in situ, and 55 cases of invasive ductal carcinoma.
As shown in Additional file 1: Table S1, Smurf2 expression was significantly associated with grade of the tumor (P < 0.001). Most of the normal/hyperplasia (87.5%), and fibrocystic (85.71%) tumors exhibited a very low expression of Smurf2. Only 1 out of the 7 fibroadenomas (14.29%) showed an intense expression of Smurf2 whereas, the remaining 6 samples (85.72%) had only mild or moderate expression of Smurf2; the same proportion as for the 7 DCIS cases. However, among the IDC cases, 33 out of the 55 IDC tumors (60.00%) dislayed a very high expression of Smurf2. Simultaneously, we also analyzed the expression levels of CNKSR2 in the same set of samples and observed a statistically significant association with tumor grade (P < 0.001). Most of the normal/hyperplasia (75.00%) and fibrocystic cases (57.14%) showed only a mild expression of CNKSR2, whereas the intensity of CNKSR2 expression increases with progression in tumor grade with 14.29% of fibroadenomas, 42.86% of DCIS and 52.73% of IDC’s showing intense expression of CNKSR2. Both Smurf2 and CNKSR2 showed a very low nuclear expression in normal luminal epithelial cells along with the cytoplasmic expression, whereas in higher grades of the tumors, the expression of Smurf2 and CNKSR2 was found to be exclusively localized in the cytoplasm. Altogether, the expression of Smurf2 and CNKSR2 displayed a statistically significant association with progressive grades of breast tumor samples as evidenced by Chi squared test.
In addition to Smurf2 and CNKSR2, we also analyzed the ER, PR, and HER2 status of the 84 representative cases, provided along with the tissue microarray data by Pantomics, and observed that only 14.29% of DCIS and 14.55% of IDC’s showed intense expression of ER compared to the normal and fibrocystic tumors (0.00%) (P < 0.001). Similar expression pattern was also observed for PR in normal and IDC cases (P < 0.05). However, the expression of HER2 was found to be significantly high in DCIS (57.14%) and IDC (41.82%) samples compared to the normal breast tissue samples (12.50%) (P < 0.05).
For further statistical analysis, we classified the total 84 breast tissue samples into two major groups (i) Normal/Benign or non-malignant (including normal/hyperplasia, fibrocystic changes and fibroadenoma, n = 22) and (ii) Malignant (including DCIS and IDC, n = 62) and on the basis of the staining intensity we classified the samples into two classes, (i) with No/Mild and (ii) with Moderate/Intense staining (Table 2). Our studies have shown that 56 out of 62 malignant tumors (90.32%) showed intense expression of Smurf2 whereas only 6 out of 22 non-malignant tumors (27.27%) showed high Smurf2 positivity (P < 0.001). Concomitantly, CNKSR2 expression also exhibited a similar pattern with 54 out of 62 malignant tumors (87.10%) showing moderate to intense expression of CNKSR2 compared with non-malignant samples, where only 5 out of 22 cases (22.73%) were found to have high expression of CNKSR2 (P < 0.001). However, the expression levels of ER and PR did not exhibit a statistically significant difference among non-malignant and malignant tumors (P = 0.875, P < 0.05) whereas HER2 was found to be intensely expressed in 35 out of 62 malignant tumors (56.45%) compared to 6 out of 22 non-mlaignant tumors (27.27%) showing a statistically significant association (P < 0.05).
Further we analyzed the association between Smurf2, CNKSR2, ER, PR, and HER2 expression with non-malignant and malignant tumors using multiple logistic regression analysis taking non-malignant tumors as the reference (Table 3). We observed that, malignant tumors were 24.88 times more likely to exhibit moderate/intense expression of Smurf2, when non-malignant tumor was the reference (OR =24.88, 95% CI: 7.05–87.79). Moreover we calculated the adjusted Odds ratio to study the actual effect of a single factor when all other factors were kept constant. According to the adjusted Odds ratio, malignant tumors were 25.94 times more likely to exhibit moderate/intense expression of Smurf2, taking non-malignant tumor as the reference (OR = 25.94, 95%CI: 3.86–174.06). Similarly, considering the unadjusted and adjusted Odds ratios of CNKSR2 expression, malignant tumors were 22.95 and 16.88 times more likely to exhibit moderate/intense expression of CNKSR2, when non-malignant tumor is the reference (unadjusted OR =22.95, 95% CI: 6.62–79.56; adjusted OR = 16.88, 95% CI: 2.64–107.82). Contrarily, ER and PR did not exhibit a statistically significant expression in malignant tumors considering non-malignant tumors as the reference. However, HER2 expression showed a statistically significant difference between non-malignant and malignant tumors. In malignant tumors there was 3.45 times higher chance for observing moderate/intense expression of HER2 when non-malignant tumors were taken as the reference (unadjusted OR =3.45, 95% CI: 1.19–10.01; adjusted OR = 2.77, 95% CI: 0.57–13.4).
Eventhough our descriptive analysis indicated a statistically significant association between Smurf2 and CNKSR2 with progressive breast tumor cases, we further analyzed the association between expression status of Smurf2 relative to CNKSR2 in non-malignant and malignant tumors (Table 4). Interestingly, among malignant tumors, 51 out of 62 cases (82.26%) showed moderate/intense expression of CNKSR2 when Smurf2 expression was moderate/intense. Only 5 out of 62 malignant tumors (8.06%) showed a no/mild expression of CNKSR2 when Smurf2 expression was moderate/intense. Simultaneously, among non-malignant tumors, 13 out of 22 cases (59.09%) showed no/mild expression of CNKSR2 when Smurf2 expression was no/mild. Only 3 out of 22 non-malignant tumors (13.64%) showed a moderate/intense expression of CNKSR2 when Smurf2 expression was no/mild. Overall, the expression pattern of Smurf2 and CNKSR2 showed a significant positive association (P < 0.001) between each other among non-malignant and malignant tumors.
Smurf2 and CNKSR2 expression is associated with the ER, PR, and HER2 status of breast tissue samples
We next observed that the expression levels of Smurf2 and CNKSR2 in relation with the hormonal (ER and PR) and HER2 status of breast tissue samples showed a statistically significant difference among non-malignant and malignant tumors (Tables 5 and 6). Our studies have shown that when ER was no/mild, 61.29 and 58.06% of malignant tumors showed moderate/intense expression of Smurf2 and CNKSR2, while only 29.03% of malignant tumors showed moderate/intense expression of Smurf2 and CNKSR2 when ER was moderate/intense. Similarly, when PR was no/mild, 66.13 and 58.06% of malignant tumors showed moderate/intense expression of Smurf2 and CNKSR2. However, when PR was moderate/intense, only 24.19 and 29.03% of malignant tumors showed moderate/intense expression of Smurf2 and CNKSR2. Contrarily, we observed that when HER2 was no/mild, only 40.32 and 38.71% of malignant tumors showed moderate/intense expression of Smurf2 and CNKSR2 whereas 50.00 and 48.39% of malignant tumors showed moderate/intense expression of Smurf2 and CNKSR2 when HER2 was moderate/intense. Overall, when the expression of ER, and PR was low, the expression of Smurf2 and CNKSR2 was high, whereas Smurf2 and CNKSR2 showed a comparatively high expression when HER2 expression was high.
Stable knockdown of Smurf2 expression restrained tumorigenic potential of breast cancer cells in a CNKSR2 dependent manner
We reported previously that transient inhibition of Smurf2 expression decreased the proliferative potential of breast cancer cells by modulating CNKSR2 mediated PI3K-AKT signaling csascade . In order to further ascertain the effect of Smurf2 knockdown on the proliferative potential of breast cancer cells, we developed stable lentiviral Smurf2 short hairpin RNA (shRNA) knockdown clones in MDA-MB-231 cell line. The downregulation of Smurf2 was confirmed by qRT-PCR, western blot and immunofluorescence (Fig. 11b, c, d). More than 90% knockdown in the levels of Smurf2 was observed in the Smurf2 shRNA clones (shSmurf2) compared to the non-target control shRNA-expressing clones (shControl). Concomitantly, the protein level expression of CNKSR2 was also found to be significantly downregulated in Smurf2 knockdown cells compared to the control cells (Fig. 11c, d). However, the CNKSR2 mRNA levels remained relatively unchanged after Smurf2 knockdown (Fig. 11b). Altogether, these data suggest that Smurf2 positively regulates CNKSR2 expression at the post-transcriptional level. Furthermore we observed that Smurf2 knockdown significantly decreases the tumorigenic potential of breast cancer cells . All these results suggest that Smurf2 plays a key role in regulating the tumorigenic properties of breast cancer cells in a CNKS2 dependent manner.
Smurf2 E3 ubiquitin ligases plays crucial physiological roles in regulating multiple cellular processes including TGF-β/BMP signaling, cell polarity, cell migration, and mitotic regulation by specifically targeting corresponding cellular substrates for ubiquitination which can either lead to stabilization and or proteasome mediated degradation [15,16,17,18]. In the present study we have demonstrated the novel regulation of the multi-functional scaffold protein CNKSR2 by the WW-HECT protein Smurf2. Consistent with the presence of the Smurf2-interacting PY motif in CNKSR2, Smurf2 was found to be immunoprecipitated with CNKSR2 and vice versa, which demonstrated a direct physical interaction between CNKSR2 and Smurf2 (Fig. 1). Interestingly, we observed that though CNKSR2 interacts with Smurf2, it does not bind to Smurf1 (Fig. 1a), which also belong to the Nedd4 family of E3 ubiquitin ligases possessing WW domains in its structure indicating specific Smurfs can recognize CNKSR2 specifically, which also provide evidence of CNKSR2 as a novel class of scaffold proteins regulated by Smurf2.
Functional activity and accessibility of Smurfs towards different substrates is mainly regulated by its subcellular localization [5, 10]. As shown in Fig. 3 we observed that both Smurf2 and CNKSR2 co-localizes particularly in the cytoplasm, eventhough a recognizable expression of Smurf2 was also observed in the nucleus. Because Smurf2 localization is highly dynamic and as previously reported Smurf2 interacts with TGF-β receptor in distinct endosomal compartments , we hypothesize that Smurf2 may be interacting mainly with the cytoplasmic CNKSR2 pool which may further reinforce the physical interaction between Smurf2 and CNKSR2, leading to its increased stability.
In order to further confirm the physical interaction between Smurf2 and CNKSR2 and to measure the kinetics of interaction, we have described for the first time, a simple and rapid, label-free, real-time, multiplex surface plasmon resonance (SPR) assay [20, 21] by which Smurf2-CNKSR2 interactions could be studied. We observed that, the results for Smurf2-CNKSR2 interaction fit well with a Langmuir model and give KD values that indicate a high affinity, and stable interaction between Smurf2 and CNKSR2 (Fig. 6 and Table 1). This is the first time, to our knowledge, that real-time Smurf2-CNKSR2 interactions have been demonstrated using SPR. We believe this approach could be extended to study the effect of a variety of other factors on the interaction.
Protein ubiquitylation can control signaling pathways by regulating the cellular levels of a protein, by controlling its subcellular localization, by preventing accumulation of defective or damaged proteins, and in some instances, by preventing protein degradation . Together with, our studies explored the consequence of the physical interaction between Smurf2 and CNKSR2, which indicated the presence of a ubiquitinated CNKSR2 in the presence of wild type Smurf2 compared with ligase deficient Smurf2 (Fig. 2c). However, Smurf2 mediated ubiquitination of CNKSR2 leads to stabilization of CNKSR2 instead of degradation as indicated by increased expression of CNKSR2 in Smurf2WT transfected cells. Unlike the interaction of Smurf2 with Mad2  and EGFR , we observed that CNKSR2 can interact with both wild type and ligase inactive mutant of Smurf2. However, the expression of endogenous CNKSR2 was found to be significantly upregulated in Smurf2WT transfected cells (Fig. 2a, b) which may be due to the editing of CNKSR2 ubiquitination by Smurf2WT, leading to increased stabilization of CNKSR2 expression. Furthermore, we demonstrated that the loss of Smurf2 caused rapid CNKSR2 degradation mediated by enhanced polyubiquitination and proteasomal degradation (Fig. 7e).
The mechanism by which Smurf2 controls CNKSR2 stability remains to be elucidated. We hypothesized that regulation of CNKSR2 by Smurf2 occurs through diverse mechanisms. Smurf2-CNKSR2 interaction exhibit a significantly high binding affinity as observed during SPR analysis and further leads to ubiquitination, which might lead to increased stability of CNKSR2 in Smurf2 overexpressed cells. Eventhough the ubiquitination of CNKSR2 by Smurf2 may increase the stability of CNKSR2; Smurf2 may target an intermediary E3 ligase for degradation to stabilize CNKSR2. This might be responsible for the comparatively increased expression of CNKSR2 in ligase deficient Smurf2C716A transfected cells also compared to the control plasmid transfected cells (Fig. 2b). Consistent with the ligase-independent function of Smurf2 is a previous report that overexpression of wild-type or ligase dead Smurf2 induces senescence . In addition, Smurf2 may sequester CNKSR2 away from cellular locations where it could encounter its E3 ligase. Alternatively, Smurf2 may instead mask regulatory epitopes for ubiquitination by other E3 ubiquitin ligases. On the other hand, Smurf2 may serve as an adaptor for an unidentified regulator that counteracts with another E3 ligase promoting CNKSR2 degradation.
Because Smurf2 and CNKSR2 were found to be involved in regulating the proliferation and invasion of breast cancer cells , we next examined the functional association of Smurf2 and CNKSR2 in the progression of breast cancer by analyzing the cellular level expression using MCF10 breast cancer progression model cell lines. Interestingly, we observed that both Smurf2 and CNKSR2 showed an integrated expression in breast cells with increasing tumorigenic potential (Fig. 8). Eventhough it is reported that Smurf2 is highly expressed in breast cancer , clinical information regarding the frequency and level of Smurf2 and CNKSR2 expression in breast cancer is incomplete, especially as regards differentiating the importance of Smurf2 and CNKSR2 expression in breast cancer subtypes with increasing tumorigenic potential including normal, usual hyperplasia, fibrocystic changes, fibroadenoma, carcinoma-in-situ (DCIS), and invasive ductal carcinoma (IDC) and its association with the ER, PR, and HER2 status of the breast tissue samples.
Using tissue microarray, which permits rapid high-throughput immunohistochemical analysis of several breast tissue samples simultaneously , Smurf2 and CNKSR2 expression was analyzed in breast cancers as well as in pre-invasive, and pre-neoplastic breast lesions and observed that our results extend the limited findings in previous reports . Concomitantly, we observed that expression of Smurf2 and CNKSR2 was associated with stage of breast tumor progression, showing increased expression from normal, hyperplastic breast samples, and fibroadenoma to in situ carcinoma to invasive breast carcinoma (Fig. 10). Eventhough we found a statistically significant independent association between Smurf2 and CNKSR2 expression with progressive breast tumor cases by means of descriptive analysis and logistic regression analysis, we further studied the association between expression status of Smurf2 relative to CNKSR2 in non-malignant (Normal/Benign) and malignant tumors (in situ and invasive breast carcinoma) (Additional file 1: Table S1, Tables 2 and 3). Despite the independent association between Smurf2 and CNKSR2 expression with progressive breast tumor stages, the expression pattern of Smurf2 and CNKSR2 showed a significant positive association (P < 0.001) between each other among non-malignant and malignant tumors (Table 4). These findings agree with the putative role of Smurf2 and CNKSR2 in proliferation and invasiveness of breast cancer.
Breast cancer is a heterogeneous disease with a wide spectrum of clinical, pathologic, and molecular features [27, 28]. Recently, Liu et al.,  reported that expression of Smurf2 is associated with the ER, PR, and HER2 status of breast tumors, which instigated us to analyze the crosstalk between Smurf2 and CNKSR2 expression with the hormonal (ER and PR) and HER2 status of breast tissue samples. Interestingly, we observed a statistically significant association between Smurf2 and CNKSR2 expression with the ER, PR, and HER2 status of non-malignant and malignant tumors (Tables 5 and 6). Overall, we observed a comparatively high expression of Smurf2 and CNKSR2 when the expression of ER and PR was low, and HER2 was high. Importantly, Smurf2 and CNKSR2 expression has been associated with features of tumor aggressivity, ER and PR negativity and HER2 overexpression.
In order to assess the physiological significance of Smurf2-CNKSR2 interaction, we stably knocked down Smurf2 using Smurf2 shRNA in MDA-MB-231 cells, and observed that Smurf2 knockdown induced CNKSR2 degradation (Fig. 11), which leads to reduced pro-proliferative and tumorigenic properties of breast cancer cells.
In summary, we illustrate a novel and specific interaction between Smurf2 and CNKSR2 which expand the list of substrates/interacting partners of Smurf2 E3 ubiquitin ligases by demonstrating that Smurf2 ubiquitinates, stabilizes, and positively regulates CNKSR2. However, the specific domain(s) involved in this interaction remains to be studied in detail. These results adopt CNKSR2 as a new family of targets by the Smurf E3 ubiquitin ligases and Smurfs as a new group of ubiquitin ligases that regulate CNKSR2 scaffold proteins. The interaction and stabilization of CNKSR2 are quite specific for the Smurf family, as they are highly preferred by Smurf2 rather than the closely related homolog, Smurf1 (Fig. 1). As reported previously  our observations have both basic as well as significant clinical relevance: (a) it identifies a molecular regulator, which may be critical in breast cancer cell–specific CNKSR2 overexpression (b) it also identifies Smurf2 as a novel therapeutic target, down-regulation of which can degrade CNKSR2 protein leading to reduced proliferation of breast cancer cells. Altogether, these findings motivate the investigation of the therapeutic efficacy of Smurf2 knockdown in treating CNKSR2-addicted cancers more effectively either as an individual therapy or in combination with already existing chemotherapy and/or radiotherapy.
Bone morphologenetic proteins
Connector enhancer of kinase suppressor of ras 2
Homologous to E6AP carboxyl terminus
Smad ubiquitin regulatory factor 2
Transforming growth factor β
Glickman MH, Ciechanover A. The ubiquitin-proteasome proteolytic pathway: destruction for the sake of construction. Physiol Rev. 2002;82:373–428.
Garrenton LS, Braunwarth A, Irniger S, Hurt E, Künzler M, Thorner J. Nucleus specific and cell cycle-regulated degradation of mitogen-activated protein kinase scaffold protein Ste5 contributes to the control of signaling competence. Mol Cell Biol. 2009;29:582–601.
Miah S, Goel RK, Dai C, Kalra N, Beaton-Brown E, Bagu ET, Bonham K, Lukong KE. BRK tgfargets Dok1 for ubiquitin-mediated proteasomal degradation to promote cell proliferation and migration. PLoS One. 2014;9:e87684.
Ardley H, Robinson P. E3 ubiquitin ligases. Essays Biochem. 2005;41:15–30.
David D, Nair SA, Pillai MR. Smurf E3 ubiquitin ligases at the cross roads of oncogenesis and tumor suppression. Biochim Biophys Acta. 1835;2013:119–28.
Du JX, Hagos EG, Nandan MO, Bialkowska AB, Yu B, Yang VW. The E3 ubiquitin ligase SMAD ubiquitination regulatory factor 2 negatively regulates Krüppel-like factor 5 protein. J Biol Chem. 2011;286:40354–64.
Therrien M, Wong AM, Rubin GM. CNK, a RAF-binding multidomain protein required for RAS signaling. Cell. 1998;95:343–53.
Fritz RD, Radziwill G. CNK1 and other scaffolds for Akt/FoxO signaling. Biochim Biophys Acta. 2011;181:1971–7.
David D, Jagadeeshan S, Hariharan R, Nair SA, Pillai MR. Smurf2 E3 ubiquitin ligase modulates proliferation and invasiveness of breast cancer cells in a CNKSR2 dependent manner. Cell Div. 2014;9:2.
Kavsak P, Rasmussen RK, Causing CG, Bonni S, Zhu H, Thomsen GH, Wrana JL. Smad7 binds to Smurf2 to form an E3 ubiquitin ligase that targets the TGFβ receptor for degradation. Mol Cell. 2000;6:1365–75.
Bravman T, Bronner V, Lavie K, Notcovich A, Papalia GA, Myszka DG. Exploring “one-shot” kinetics and small molecule analysis using the ProteOn XPR36 array biosensor. Anal Biochem. 2006;358:281–8.
Schmittgen TD, Livak KJ. Analyzing real-time PCR data by the comparative CT method. Nat Protoc. 2008;3:1101–8.
Franken NA, Rodermond HM, Stap J, Haveman J, Van Bree C. Clonogenic assay of cells in vitro. Nat Protoc. 2006;1:2315–9.
Jin C, Yang Y, Anver MR, Morris N, Wang X, Zhang YE. Smad ubiquitination regulatory factor 2 promotes metastasis of breast cancer cells by enhancing migration and invasiveness. Cancer Res. 2009;69:735–40.
Ebisawa T, Fukuchi M, Murakami G, Chiba T, Tanaka K, Imamura T, Miyazono K. Smurf1 interacts with transforming growth factor-β type I receptor through Smad7 and induces receptor degradation. J Biol Chem. 2001;276:12477–80.
Narimatsu M, Bose R, Pye M, Zhang L, Miller B, Ching P, Sakuma R, Luga V, Roncari L, Attisano L. Regulation of planar cell polarity by Smurf ubiquitin ligases. Cell. 2009;137:295–307.
Ozdamar B, Bose R, Barrios-Rodiles M, Wang HR, Zhang Y, Wrana JL. Regulation of the polarity protein Par6 by TGFß receptors controls epithelial cell plasticity. Science. 2005;307:1603–9.
Zhu H, Kavsak P, Abdollah S, Wrana JL, Thomsen GH. A SMAD ubiquitin ligase targets the BMP pathway and affects embryonic pattern formation. Nature. 1999;400:687–93.
Di Guglielmo GM, Le Roy C, Goodfellow AF, Wrana JL. Distinct endocytic pathways regulate TGF-β receptor signalling and turnover. Nat Cell Biol. 2003;5:410–21.
Stravalaci M, Bastone A, Beeg M, Cagnotto A, Colombo L, Di Fede G, Tagliavini F, Cantù L, Del Favero E, Mazzanti M. Specific recognition of biologically active amyloid-β oligomers by a new surface plasmon resonance-based immunoassay and an in vivo assay in Caenorhabditis elegans. J Biol Chem. 2012;287:27796–805.
Subramanian K, Fee CJ, Fredericks R, Stubbs RS, Hayes MT. Insulin receptor-insulin interaction kinetics using multiplex surface plasmon resonance. J Mol Recognit. 2013;26:643–52.
Yang B, Kumar S. Nedd4 and Nedd4-2: closely related ubiquitin-protein ligases with distinct physiological functions. Cell Death Differ. 2009;17:68–77.
Osmundson EC, Ray D, Moore FE, Gao Q, Thomsen GH, Kiyokawa H. The HECT E3 ligase Smurf2 is required for Mad2-dependent spindle assembly checkpoint. J Cell Biol. 2008;183:267–77.
Ray D, Ahsan A, Helman A, Chen G, Hegde A, Gurjar SR, Zhao L, Kiyokawa H, Beer DG, Lawrence TS. Regulation of EGFR protein stability by the HECT-type ubiquitin ligase SMURF2. Neoplasia. 2011;13:570–IN571.
Zhang H, Cohen SN. Smurf2 up-regulation activates telomere-dependent senescence. Genes Dev. 2004;18:3028–40.
Kononen J, Bubendorf L, Kallionimeni A, Bärlund M, Schraml P, Leighton S, Torhorst J, Mihatsch MJ, Sauter G, Kallionimeni OP. Tissue microarrays for high-throughput molecular profiling of tumor specimens. Nat Med. 1998;4:844–7.
Onitilo AA, Engel JM, Greenlee RT, Mukesh BN. Breast cancer subtypes based on ER/PR and Her2 expression: comparison of clinicopathologic features and survival. Clin Med Res. 2009;7:4–13.
Pinhel I, Hills M, Drury S, Salter J, Sumo G, A’hern R, Bliss JM, Sestak I, Cuzick J, Barrett-Lee P. ER and HER2 expression are positively correlated in HER2 non-overexpressing breast cancer. Breast Cancer Res. 2012;14:R46.
Liu X, Gu X, Sun L, Flowers AB, Rademaker AW, Zhou Y, Kiyokawa H. Downregulation of Smurf2, a tumor-suppressive ubiquitin ligase, in triple-negative breast cancers: involvement of the RB-microRNA axis. BMC Cancer. 2014;14:57.
Adams J. The proteasome: a suitable antineoplastic target. Nat Rev Cancer. 2004;4:349–60.
We thank Dr. Suresh Kumar Rayala for providing MCF10 AT and MCFDCIS breast cell lines and Dr. Jem Prabhakar for providing breast tissue samples. We also thank Mr. Anurup for help in confocal microscopy.
We thank the Department of Biotechnology (DBT), Government of India for the financial support to DD (DBT Award No: DBTJRF/0809/37) and Rajiv Gandhi Centre for Biotechnology (RGCB) for providing all the instrumental facilities for collection of data, analysis and interpretation.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
Immortalized normal human breast epithelial cell line MCF10A, and the human breast cancer MCF-7 and MDA-MB-231 cells were purchased from American Type Culture Collection (ATCC; Manassas, VA, USA) and collected from cell repository of Rajiv Gandhi Centre for Biotechnology. The pre-malignant and in situ grade cell lines-MCF10AT and MCFDCIS were a kind gift from Prof.Suresh Kumar Rayala (Indian Institute of Technology-Madras, India). Human breast tissue samples were collected from Regional Cancer Centre (RCC), Thiruvananthapuram, India after obtaining approval from the Institutional Human Ethics Committee HEC No. 42/2008, Regional Cancer Centre, Thiruvananthapuram. The samples were collected from patients who underwent primary surgery without prior chemotherapy or radiotherapy. Informed written consent was taken from all the patients prior surgery/excision of tissue.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.