- Research article
- Open Access
TIMP-2 regulates proliferation, invasion and STAT3-mediated cancer stem cell-dependent chemoresistance in ovarian cancer cells
BMC Cancer volume 20, Article number: 960 (2020)
The metzincin family of metalloproteinases and the tissue inhibitors of metalloproteinases (TIMPs) are essential proteins required for biological processes during cancer progression. This study aimed to determine the role of TIMP-2 in ovarian cancer progression and chemoresistance by reducing TIMP-2 expression in vitro in Fallopian tube secretory epithelial (FT282) and ovarian cancer (JHOS2 and OVCAR4) cell lines.
FT282, JHOS2 and OVCAR4 cells were transiently transfected with either single or pooled TIMP-2 siRNAs. The expression of different genes after TIMP-2 knock down (T2-KD) or in response to chemotherapy was determined at the mRNA level by quantitative real time PCR (qRT-PCR) and at the protein level by immunofluorescence. Sensitivity of the cell lines in response to chemotherapy after TIMP-2 knock down was investigated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and 5-Ethynyl-2′-deoxyuridine (EdU) assays. Cell invasion in response to TIMP-2 knockdown was determined by xCELLigence.
Sixty to 90 % knock down of TIMP-2 expression was confirmed in FT282, OVCAR4 and JHOS2 cell lines at the mRNA and protein levels. TIMP-2 knock down did not change the mRNA expression of TIMP-1 or TIMP-3. However, a significant downregulation of MMP-2 in T2-KD cells occurred at both the protein and activation levels, compared to Control (Cont; scrambled siRNA) and Parental cells (P, transfection reagent only). In contrast, membrane bound MT1-MMP protein levels were significantly upregulated in T2-KD compared to Cont and P cells. T2-KD cells exhibited enhanced proliferation and increased sensitivity to cisplatin and paclitaxel treatments. Enhanced invasion was observed in the T2-KD-JOSH2 and OVCAR4 cells but not in T2-KD-FT282 cells. Treatment with cisplatin or paclitaxel significantly elevated the expression of TIMP-2 in Cont cells but not in T2-KD cells, consistent with significantly elevated expression of chemoresistance and CSC markers and activation of STAT3. Furthermore, a potent inhibitor of STAT3 activation, Momelotinib, suppressed chemotherapy-induced activation of P-STAT3 in OVCAR4 cells with concomitant reductions in the expression of chemoresistance genes and CSC markers.
The above results suggest that TIMP-2 may have a novel role in ovarian cancer proliferation, invasion and chemoresistance.
Worldwide, of the 250,000 women who are diagnosed annually with ovarian cancer, about 140,000 die within 5 years. Ovarian cancer patients have the lowest survival rate among gynaecological cancers . Despite a high initial response to debulking surgery and first line chemotherapy consisting of taxane and platinum-based drugs, almost all patients relapse within a few months with a chemoresistance-associated disease, a trend that remains stagnant for the last three to four decades . Even though different mechanisms of chemoresistance have been described [2, 3], none have had an individual impact in a clinical setting. Hence, a more detailed knowledge of the biological mechanisms leading to chemoresistance is essential to achieve a better treatment outcome for persistent recurring ovarian cancer patients.
Matrix metalloproteinases (MMPs) are members of the metzincin family that facilitate extracellular matrix (ECM) degradation and thereby promote tumour angiogenesis, invasion and metastasis [4,5,6]. Conversely, tissue inhibitors of MMPs (TIMPs) are multifunctional proteins, which belong to a family of secreted and ECM bound proteins that naturally inhibit the proteolytic activity of MMPs [7, 8]. The four TIMP family members, TIMP-1, − 2, − 3 and − 4 share a substantial homology in their sequences . Of all the TIMPs, TIMP-2 only interacts with a cell-membrane bound MMP, commonly known as MT1-MMP and can act as either an initiator or an inhibitor of MMP-2 activation. As an initiator of MMP-2 activation, the catalytic domain of MT1-MMP binds to the N-terminal region of TIMP-2. This leaves the C-terminal region of TIMP-2 free for binding to the hemopexin-like domain of pro-MMP-2 . This ternary MT1-MMP-TIMP2 complex facilitates assembly of the extracellular secreted pro-MMP-2 on the cell surface in close proximity to TIMP-free active MT1-MMP. TIMP-free MT1-MMP then cleaves the pro-peptide from cell membrane bound pro-MMP-2 to produce mature MMP-2. In cases where TIMP-2 acts as an inhibitor of MMP-2, the C-terminal end of TIMP-2 acts as a receptor for the C-terminal region of MMP-2, binding of which prevents the interaction of TIMP-2 with MT1-MMP, thereby preventing subsequent MMP-2 activation .
The expression of TIMP-2 is universal in most cell types where it functions as an endogenous inhibitor of MMPs . In addition to its MMP-2 dependent functions, TIMP-2 can regulate signalling pathways by direct interaction with the cell surface receptors on normal and cancer cells [12, 13]. TIMP-2 also mediates anti-angiogenic effects by inhibiting endothelial cell migration and invasion through α3β1 integrin . The tumour microenvironment may provide paracrine cues that regulate these TIMP-2-dependent roles in cancer cells .
The concept that cancer stem cells (CSCs) are small populations of slowly proliferating, drug resistant cells that contribute to tumour initiation and progression, relapse and metastasis has gained substantial importance [16, 17]. Standard cancer therapies usually target and kill actively proliferating cancer cells thereby reducing tumour burden and decreasing cancer-associated symptoms. This however, does not remove the small population of drug-resistant CSCs. As a result, CSCs can contribute to persistent residual disease even after effective anti-cancer treatments. Hence, it has been proposed that CSCs initiate cancer relapse, which ultimately results in mortality. We and others, have previously shown a correlation between activated STAT3 pathway and the existence of chemoresistance-associated CSCs in residual tumours [18, 19, 20, 21]. Activated STAT3 was shown to be essential for the sustenance of glioblastoma stem cells , fast proliferating intestinal  and mammary stem cells . In addition, the activated STAT3 pathway has been associated with the progression and chemoresistance in ovarian and other cancers [25, 26].
In this study, we report significantly elevated expression of TIMP-2 in high-grade serous compared to benign ovarian tumours. By using siRNA, we examined the effect of TIMP-2 knock down (T2-KD) on MT1-MMP and MMP-2 expression levels, proliferation, invasion and chemosensitivity in Fallopian tube secretory epithelial cells and two ovarian cancer cell lines. We demonstrate that T2-KD cells are associated with increased expression of MT1-MMP and decreased expression and activity of MMP-2 in ovarian cancer and Fallopian tube epithelial cells. The knock down of TIMP-2 resulted in enhanced cell proliferation and increased sensitivity to chemotherapy treatments in ovarian cancer and Fallopian tube epithelial cells. However, increased invasion was only observed in ovarian cancer T2-KD cells but not in T2-KD Fallopian tube cells. Increased sensitivity to chemotherapy in T2-KD cancer cells was associated with an inability to activate the STAT3 pathway and a consequent deficit in chemotherapy resistance and CSC traits. These data reveal a potential role of TIMP-2 in the regulation of proliferation, invasion and chemoresistance in ovarian cancer cells and identifies TIMP-2 as a potential target to circumvent chemoresistance in ovarian cancer.
Patients and tissue samples
Ovarian tumours were acquired from ovarian cancer patients admitted to The Royal Women’s Hospital after procuring written consents under officially accepted ethical approval (Ethics approval #09/09) by the Research and Ethics Committee of Royal Women’s Hospital, Melbourne, Australia. High-grade serous epithelial ovarian tumours were obtained from seventeen patients undergoing surgery at the Oncology Dysplasia Unit of The Royal Women’s Hospital, Melbourne, Australia. Eight normal/benign samples were obtained from patients undergoing abdominal hysterectomy or bilateral salpingo-oophorectomy due to pre-existing medical conditions. At the time of collection, tissues were fixed in 4% paraformaldehyde. Information on tumour grade, stage and histopathology for individual tumour was obtained from pathology reports. The clinical information on each tumour sample is described in Table 1. Patients recruited in this study did not undergo treatment with chemotherapy, immunotherapy or radiation.
Immunohistochemistry and quantitative analysis of protein expression
Immunohistochemistry staining of tumours was outsourced to the Anatomical Pathology Laboratory Services at The Royal Children’s Hospital, Melbourne, Australia. Briefly, paraffin embedded tissue samples were sectioned at 4 μm thickness and stained using 1:100 TIMP-2 polyclonal antibody (PAB11827, Abnova, Taipei, Taiwan) and OptiView DAB IHC Detection kit (Ventana Medical Systems, Inc., Arizona, USA). The samples were processed on Ventana Benchmark Immunostainer (Ventana Medical Systems, Inc., Arizona, USA) as described previously . Negative controls used in this study were prepared by incubating samples in diluent without primary antibodies followed by the secondary antibody. Sections of human placental and tonsil tissues were used in each slide as positive controls to determine the staining efficiency of the antibodies used. Stained slides were then scanned at X40 magnification by the Southern Health Tissue Bank at Monash Medical Centre (Victoria, Australia) using the Aperio Scanscope XT (Aperio-Leica Microsystems Pty Ltd) and imaged using the Aperio ImageScope v184.108.40.20613 software (Leica Biosystems Pathology Imaging 2003–2016). Sections were evaluated microscopically for positive DAB staining in conjunction with positive CA125 (Ventana Medical Systems, Inc., Arizona, USA) staining. Three to eight random areas were selected and DAB positivity over each of these areas was calculated and divided by the average of negative control of each group. Results were plotted on a bar graph using PRISM software.
Two established ovarian cancer cell lines were used for this study. JHOS2 (cell line derived from a primary tumour of a patient with high-grade serous cystadenocarcinoma, original repository: RIKEN, catalogue RCB 1521) [27, 28] and OVCAR4 (a cell line derived from the ascites of a patient diagnosed with ovarian serous adenocarcinoma, pre-treated with cyclophosphamide cisplatin and doxorubicin chemotherapies, Cellosaurus cell line, CVCL_1627) . These cell lines were obtained from Professor David Bowtell (Peter MacCallum Cancer Centre, Parkville, Australia). The immortalised Fallopian tube secretory epithelial cell line, FT282, used as a non-cancer control, was a gift from Professor Ronny Drapkin (University of Pennsylvania)  and was obtained from Professor David Bowtell’s laboratory in Peter MacCallum Cancer Centre, Melbourne Australia.
OVCAR4 cells were maintained in RPMI-1640 (Sigma-Aldrich, Sydney, Australia); JHOS2 and FT282 were maintained in F-12 and DMEM medium (1:1). Each cell line medium was supplemented with L-glutamine (2 mM), and antibiotics (Fungizone, streptomycin and penicillin 1% v/v) and FBS (10% v/v) with the exception of the FT282 cell line which was supplemented with Ultroser™ G serum substitute (PALL, Life Sciences, NY, USA) instead of FBS. JHOS2 culture medium was supplemented with non-essential amino acids (1% v/v). Cell lines were maintained at 37 °C in 5% CO2. All cell lines were passaged at least twice a week once they reached a confluence of 65–80%.
Transient transfections of cell lines
Three unique 27mer small interfering RNA (siRNA A, B, C) duplexes directed against human TIMP-2 (OriGene Technologies, SR304838, MD, USA) and a pooled siRNA (A + B + C) directed against TIMP-2 were used to knock down TIMP-2 expression (T2-KD) in FT282, JOSH-2 and OVCAR4 cell lines. A Universal non-targeting siRNA duplex was used as a Control (Cont) (OriGene Technologies, SR30004, MD, USA) in these experiments. To avoid off-target effects, the lowest TIMP-2 siRNA concentrations were optimized for each cell line (range tested was from 1 nM to 10 nM) and transfected cells were collected for RNA analysis 48 h after transfection. Transfection efficiency for each cell line was evaluated by using 15 nM siGLO™ Red Transfection Indicator (Dharmacon) as per manufacturer’s instructions. Parental cells (P) were cells treated with transfection reagent but no siRNA. Untreated cells (Unt) are parental cells without any treatment.
Immunofluorescence analysis was conducted on cell lines as described previously . Briefly, 1 X 104 cells were cultured overnight on 8-well chamber slides (Lab-Tek II Chamber Slide System) in complete growth medium at 37 °C in 5% CO2. Next day the cells were fixed with paraformaldehyde (PFA)/PBS solution, permeabilized using 0.1 (v/v) Triton X-100 (Sigma-Aldrich) in PBS, washed with cold PBS and incubated for 2 h with blocking buffer (1% BSA/PBS) followed by primary antibody treatment overnight at 4 °C (Table 2). Cells were stained with appropriate secondary antibodies (1:200 dilutions) (Table 2) in blocking buffer for 2 h. DAPI (4′,6-diamidino-2-phenylindole) (Invitrogen, Carlsbad, USA) was used to stain cellular nuclei at a 1:2000 dilution for 10 min at room temperature. Fluorescence imaging was visualized using an OLYMPUS BX53F upright microscope (Olympus, Tokyo, Japan) and images were taken using an Olympus DP70 camera and the Olympus CellsSens Dimension version 1.7.1 software (Olympics Corporation). The microscope filter parameters used for the individual fluorophore are provided in the supplementary Table 1. To avoid biased measurements, equal intensity acquisition parameters were set prior to imaging (for example the fluorophores DAPI acquisition time was set at 5 ms, Alexa 488 at 300 ms, Alexa 568 at 150 ms and Alexa 594 at 450 ms). The intensity units were measured using FIJI analysis software [ImageJ software 1.51j8 (Wayne Rasband National Institute of Health, USA)] according to DAPI location. This was repeated at least 4–9 times for each photograph and at least two images were taken for each well.
For zymography analysis, complete growth media was discarded and replaced by OPTIMEM media (GIBCO Life Technology, NY, USA). The serum free medium was collected and concentrated using 10 kDa Amicon ultra-4 spin columns (Merck-Millipore, Billerica, MA, USA). Secreted proteins in the conditioned medium were separated using SDS-PAGE gel (10%) containing 1% gelatin as described previously . The gels were stained with Coomassie Blue, and distained at room temperature. To measure MMP activities, gels were incubated in 10 mM EDTA (Fisher, Fair Lawn, NJ USA) and a proteolytic inhibitor, as described previously . Bands were visualized and analysed using the Fuji Film LAS-3000 gel doc system and the Image Lab software version 6.0.0 (Bio-Rad Laboratories, Inc., Gladesville, NSW, Australia). Semi-quantitative densitometry analysis was performed using Image J software 1.51j8 (Wayne Rasband National Institute of Health, USA).
This was performed as described previously [19, 31]. Cells (3X104) were seeded and transfected in 96-well plates on the same day and after 24 h, cell culture medium was replaced. Chemotherapy (paclitaxel or cisplatin) at different concentrations (0 to 320 μg/ml) was added to cells for 48 h after which culture medium was replaced and 100 μL of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) (MTT) solution (Sigma-Aldrich) dissolved in 1x PBS solution (0.5 mg/ml, final concentration) (Sigma-Aldrich) was added to the cells. After 2 h incubation, cell culture medium was replaced with 100 μl of dimethyl sulfoxide (DMSO). Absorbance was read at OD595nm using the CLARIOstar Plate Reader (BMG Labtech, Germany) and MARS Data Analysis Computer Software (BMG Labtech, Mornington, Victoria, Australia).
This assay was performed using the Click-IT™ Plus EdU Flow Cytometry Assay Kit (Invitrogen/Thermo Fisher Scientific North Ryde, NSW, Australia) essentially as described previously . Briefly, 2X104 cells were grown and transfected in 24-well plates for 48 h prior to the assay. 5-Ethynyl-2′-deoxyuridine (EdU) was added at a final concentration of 10 μM and the cells were incubated for 1 h at 37 °C. Cells were trypsinized, centrifuged at 1200 rpm for 5 min and washed with 1% BSA in PBS and fixed in Click-IT fixative. Cell pellets were washed with Perm-wash buffer, stained with Alexa Fluor 647 Picoyl Azide, washed in Perm-wash and resuspended in Perm-wash containing 20 μg/ml propidium iodide. The cells were then analysed by flow cytometer using 633/635 nm excitation with a red emission filter for the detection of Alexa Fluor 647 Azide. Single cells were gated using forward scatter height vs area. Single cells were then plotted according to EdU/Alexa 647 Azide (Log scale, y-axis) to identify cells in S-phase based on incorporation of EdU and PI staining (linear scale, x-axis) and to separate cells in G0/G1, S-phase and G2/M based on DNA content. Cells for which EdU or Alexa 647 Azide were omitted were used as negative controls for EdU staining.
Cell invasion assay was performed by using the Roche xCELLigence DP instrument as described previously . The upper chamber of the 16-well CIM plate (Roche, NSW, Australia) was coated with 20 μl of matrigel and left to set for 30 min at 37 °C. Cells (4X104) suspended in 130ul Gibco® Opti-MEM™ Media (Thermo-Fisher Scientific, NSW, Australia) were seeded on the top compartment of the pre-equilibrated 16-well CIM plate (Roche). Readings were taken every 15 min for ~ 40 h. Each plate contained two duplicate wells and each experiment was repeated 3 times. Mean values from three experiments on each Cont and T2-KD cell lines are illustrated graphically using PRISM software. Linear regression analysis of two slopes arising from Cont and T2-KD cells were used to obtain significant values.
RNA extraction, quantitative and relative real-time PCR (qRT-PCR)
RNA was extracted from chemotherapy-treated (cisplatin or paclitaxel) and untreated cell lines using TRIzol® reagent (Ambion-Life Technologies, Carlsbad, CA, USA) followed by the chloroform: phenol method as described previously . Five hundred ng of total RNA was reverse transcribed using the high capacity cDNA Reverse Transcription Kit (Applied Biosystems, CA, USA) and qRT-PCR amplification was performed using the Applied Biosystems ViiA 7 Real-Time PCR (Thermo Fisher Scientific, NSW, Australia) as described previously . Table 3 lists the sequences and accession numbers of genes analysed. Data are presented as absolute values (fg) normalized to 18S (Fig. 2a)  or relative expression normalized to housekeeping gene 18S [Fig. 3 (b-c), Fig. 5 (a-d), Fig. 6 (c-e), Fig. 7 (b-c), Fig. 8 (a-b) and Fig. 9 (b-e)].
When only two treatment groups were compared, an unpaired Man-Whitney’s non-parametric t-test was used. However, when more than two treatment groups were compared a One-Way ANOVA was used. Data are presented as mean ± standard error of the mean (SEM). xCELLigence data was analysed by linear regression analysis, and presented as the standard deviation (SD) of the mean. For statistical significance, the probability levels adopted were p < 0.05(*), p < 0.01(**), p < 0.001 (***) and p < 0.0001 (****). All data were analysed by Graph Pad PRISM software and Microsoft Excel 2016. All experiments were performed for a minimum of three times (unless otherwise indicated) in triplicate.
The expression of TIMP-2 is significantly higher in human serous high-grade ovarian tumours compared to benign tumours
Twenty-five paraffin embedded tissues (Table 1), consisting of eight benign serous ovarian tumours and seventeen poorly differentiated high-grade serous tumours were analysed by immunohistochemistry using an anti-human TIMP-2 specific antibody. In > 90% tumours TIMP-2 expression was noted in the epithelial tumour cells also expressing CA-125, while in a few others stromal expression of TIMP-2 was also noted (Fig. 1a). Staining was mostly confined to the cytoplasm but in some cases, discrete membrane staining of the tumour cells was also evident (Fig. 1a). Diffuse TIMP-2 staining was noted in the stroma of some tumours, which was mainly cytoplasmic. In the case of benign tumours, only the ovarian surface epithelium stained positive for TIMP-2. The staining was weak and confined mainly to the cytoplasm. Expression of TIMP-2 was significantly enhanced in high-grade ovarian tumours compared to benign tumours (Fig. 1b).
Expression of TIMPs, MMP-2 and MT1-MMP in a normal fallopian tube and two ovarian cancer cell lines
The mRNA expression of TIMP-1, − 2 and − 3 was measured in the ovarian cancer cell lines, JHOS2 and OVCAR4 and a Fallopian tube secretory epithelial cell line, FT282, which was used as a non-cancer control (Fig. 2a). All three cell lines expressed mRNA for TIMP-1, − 2 and − 3, with TIMP-2 mRNA expression being several-fold greater than the other TIMPs in each cell line. TIMP-2, MMP-2 and MT1-MMP protein was also detected using immunofluorescence in all three cell lines (Fig. 2b, Supplementary Fig. 1), but all three proteins were detected at higher levels in OVCAR4 cells compared to JHOS2 and FT282 cells.
Reduction of TIMP-2 expression by siRNA had no significant effect on the expression of TIMP-1 and TIMP-3 mRNAs in the normal fallopian tube and ovarian cancer cell lines
To assess the function of TIMP-2 in cancer cell lines, the expression of TIMP-2 was knocked down in ovarian cancer cell lines JOSH2 and OVCAR4 and FT282 Fallopian cell line using three unique 27mer siRNA duplexes individually, or a pooled siRNA duplex directed against human TIMP-2 (T2-KD). A non-targeting universal siRNA was used as a Control (Cont) in these experiments. TIMP-2 protein expression was reduced by 90% in FT282 and 80% in both JOSH2 and OVCAR4 cell lines compared to Cont and Parental (P) cell lines using pooled TIMP-2 siRNA (Fig. 3a, Supplementary Fig. 2). Similar trends of TIMP-2 mRNA knockdown, 60% in FT282 cell line and 80% in both JOSH2 and OVCAR4 cell lines was observed using single 27mer TIMP-2 siRNA duplexes or with the pooled TIMP-2, siRNAs compared to Cont and Parental (P) cell lines (Fig. 3b, Supplementary Fig. 3A). However, knock down of TIMP-2 in FT282; JOSH2 and OVCAR4 cell lines had no significant effect on the mRNA expression of TIMP-1 and TIMP-3 (Fig. 3b, Supplementary Figs. 3 B-C).
Reduction of TIMP-2 mRNA expression significantly enhanced the expression of MT1-MMP but decreased the activation and expression of MMP-2
As TIMP-2 is known to regulate MT1-MMP and MMP-2 by its direction interaction with these proteases, we next assessed the effect of TIMP-2 knockdown on the expression of MT1-MMP and MMP2. FT282, OVCAR4 and JHOS2 T2-KD cells had significantly enhanced expression of MT1-MMP compared to corresponding Cont and P cells as shown by immunofluorescence (Fig. 4a). However, MMP-2 expression was significantly downregulated after TIMP-2 knock down compared to Cont and P cells in the three cell lines studied (Fig. 4b). Consistent with the immunofluorescence analyses, zymography showed decreased activation of MMP-2 and lower expression of the pro-zymogen form of MMP-2 in T2-KD OVCAR4 and JHOS2 cells compared to Cont and P cells (Fig. 4c).
As the expression of E-cadherin (E-Cad) has been shown to decrease with upregulation of MT1-MMP in many cancer cell lines , we compared the mRNA expression of E-Cad in T2-KD cells with the corresponding Cont and P cells (Fig. 5a). Significantly, decreased mRNA expression of E-Cad was observed in T2-KD FT282 and OVCAR4 cells compared to matched Cont and P cell (Fig. 5a). However, no such decrease in E-Cad expression was observed in T2-KD JHOS2 cells compared to its matched control. To determine if the decrease in E-Cad expression correlated with an increase in N-cadherin (N-Cad) and vimentin (VIM) expression, consistent with an epithelial mesenchymal transition (EMT) pattern in these cells, the mRNA expression of N-Cad and VIM was investigated. A significant increase in the expression of N-Cad was noted in T2-KD OVCAR4 cells and an increasing trend in T2-KD JOSH2 and FT282 cells, compared to Cont and P cells (Fig. 5b). The mRNA expression of VIM was significantly upregulated in JHOS-2 and FT282 T2-KD cells compared to their respective control cells (Fig. 5c). However, T2-KD OVCAR4 cells showed an increasing trend in VIM mRNA expression compared to corresponding controls (Fig. 5c).
In order to determine if the classical EMT pathway  was influenced by the knock down of TIMP-2, we evaluated the mRNA expression of three known EMT transcription factors, SLUG, TWIST and SNAIL in T2-KD FT282, JOSH2 and OVCAR4 cells, and their relevant Cont and P cells. However, there was no change in the expression of SLUG and TWIST in T2-KD FT282 and JOSH2 cells compared to Cont and P cells (Supplementary Fig. 4), and neither TWIST nor SLUG expression was detectable in OVCAR4 cell line.
As MT1-MMP dependent collagen degradation promotes remodelling of tissues during cancer progression , we determined the expression of collagen 12A1 (COL12A1, fibril associated collagen that modifies the interaction between collagen 1 and the surrounding matrix) in FT282, OVCAR4 and JHOS2 cells following TIMP-2 knockdown. The suppression of TIMP-2 in all three cell lines correlated with a significant decrease in COL12A1 mRNA expression compared to their respective Cont and P cells (Fig. 5d). These results suggest that enhancement in MT1-MMP expression due to loss of TIMP-2 in FT282; OVCAR4 and JHOS2 cells may enhance collagen degradation-dependent extracellular matrix remodelling.
Reduction of TIMP-2 expression significantly enhanced the proliferation of FT282 and JOSH2 and OVCAR4 cell lines but enhanced invasion was observed only in JOSH2 and OVCAR4 cell lines
The proliferation of T2-KD FT282, OVCAR4 and JHOS2 and the relevant Cont and P cells was analysed 48 h after siRNA transfection using the MTT assay (Fig. 6a) and by measuring EdU (5-ethynyl-2′-deoxyuridine) incorporation into DNA using flow cytometry (Fig. 6b, Supplementary Fig. 5). Both assays revealed a significant enhancement in cellular proliferation in all T2-KD cells compared to the matched Cont and P cells. To further characterize the proliferative capacity of T2-KD cells, we evaluated the mRNA expression of the cell cycle enzymes, CDC25A, CDC25B and CDC25C . The expression of CDC25B was significantly upregulated in T2-KD FT282, OVCAR4 and JHOS2 cells compared to their respective control cells (Fig. 6c). However, CDC25C was only upregulated in T2-KD OVCAR4 and JOSH2 cancer cells compared to their corresponding control cells (Fig. 6d) and there was no change in the expression of CDC25A in any of the T2-KD cells compared to its respective controls (Fig. 6e).
We next evaluated the invasive capacities of T2-KD cells by xCELLigence Real Time Cell Analysis. This revealed a significant enhancement of invasion through Matrigel by T2-KD JOSH2 and OVCAR4 cells compared to the respective control cells. In contrast, non-cancerous FT282 T2-KD cells showed significantly decreased invasion compared to the relevant control cells (Fig. 6f).
Reduction of TIMP-2 expression enhanced cell sensitivity to chemotherapy
Next, we evaluated the response of T2-KD FT282, JOSH2, OVCAR4 cells and their corresponding controls to cisplatin and paclitaxel-based chemotherapy, standard drugs used for the cure of ovarian cancer patients. All three cell lines showed enhanced sensitivity to paclitaxel and cisplatin in response to T2-KD as shown by the reductions in IC50 values (50% cell killing) (7A). The T2-FT282 cell line was more sensitive to both chemotherapeutic agents than the cancer cell lines. The IC50 value in the T2-KD FT282 cell line was reduced 800–1000 fold by both paclitaxel and cisplatin treatments (Fig. 7a). However, in the OVCAR4 cell line there was a 5–6 fold decrease in the IC50 values in chemotherapy-treated T2-KD cells compared to the corresponding control cells (Fig. 7a). T2-KD JHOS2 cell line showed 3–5-fold lower IC50 values in response to chemotherapy treatment compared to its matched control (Fig. 7a).
Chemotherapy treatments regulated MT1-MMP and MMP-2 in a TIMP 2 dependent manner
To determine if chemotherapy treatments have any effect on the expression of TIMP-2, MT1-MMP and MMP-2, mRNA and protein levels were evaluated in the OVCAR4 cells before and after chemotherapy treatments and TIMP-2 knock down. Treatment of OVCAR4 cells with individual IC50 doses of paclitaxel or cisplatin significantly enhanced TIMP-2 mRNA and protein levels compared to untreated Cont cells (Fig. 7b). However, this response to paclitaxel and cisplatin was not observed in T2-KD cells as TIMP2 was expressed at only basal levels following TIMP2 knock down (Fig. 7b).
Consistent with our earlier experiments (Fig. 4a), the basal protein expression of MT1-MMP was higher and MMP-2 was lower in T2-KD compared to Cont OVCAR4 cells in the absence of paclitaxel or cisplatin (ie untreated control – column 1 compared to column 4, Fig. 7c). As in the case of TIMP-2, both paclitaxel or cisplatin treatment substantially increased MT1-MMP and MMP-2 mRNA and protein levels in Cont cells (Fig. 7c, columns 2 and 3 compared to column 1 in each graph). In contrast, while MT1-MMP and MMP-2 mRNA still increased in T2-KD cells in response to chemotherapy, this effect was substantially blunted in T2-KD cells compared to Cont cells (Fig. 7c, columns 5 and 6 compared to 4 in each graph). Similarly, while MMP-2 protein increased in T2-KD cells in response to cisplatin and paclitaxel, this response was blunted by TIMP-2 knock down. Interestingly, this TIMP-2 knock down dependent blunting effect appeared more pronounced in paclitaxel treatment group than in the cisplatin treatment (Fig. 7c). While the MT1-MMP protein levels appeared reduced in T2-KD cells compared to the cisplatin or paclitaxel treated Cont cells, there was no difference between the untreated T2-TD cells compared to those treated with paclitaxel or cisplatin (Fig. 7c).
Chemotherapy treatments enhanced chemoresistance and CSC markers in a TIMP2 dependent manner
In order to explore further the mechanisms by which knock down of TIMP-2 increased chemosensitivity in OVCAR4 cells, we evaluated the expression of two chemoresistance markers, DNA excision repair complex protein 1 (ERCC1) and tubulin β type III (TUBB3), and cancer stem cell (CSC) markers [Pou5f1 (OCT4), CD44, CD133 and EpCAM)] at the mRNA and protein levels. The expression of both chemoresistance and all CSC markers were significantly enhanced at the mRNA and protein levels in Cont OVCAR4 cells in response to either chemotherapy treatment (Fig. 8a and b). However, the enhancement level of chemoresistance and CSC markers was substantially blunted in T2-KD OVCAR4 cells compared to Cont OVCAR4 cells, strongly indicating that the upregulation of these chemoresitance and CSC markers in response to either chemotherapy agent is TIMP-2 dependent.
Chemotherapy treatment enhanced STAT3 phosphorylation in a TIMP2 dependent manner
We previously reported that phosphorylation of STAT3 (P-STAT3) occurs in response to chemotherapy treatments in ovarian cancer cell lines [18, 19, 31]. Consistent with our previous findings, OVCAR4 cells exhibited significantly enhanced STAT3 phosphorylation in response to either paclitaxel or cisplatin treatment (Fig. 8c). However, this response was abolished when TIMP-2 was reduced in the T2-KD OVCAR4 cells (Fig. 8c). The level of total STAT3 (T-STAT3) remained unchanged in response to all treatments.
Chemotherapy dependent upregulation of chemoresistance and CSC markers requires STAT3 signalling and is correlated with a loss of TIMP-2 expression
We next used a JAK2/STAT3 specific inhibitor, Momelotinib, to determine whether chemotherapy dependent upregulation of chemoresistance and CSC and markers depended on STAT3 signalling in OVCAR4 P cells. Momelotinib specifically inhibited cisplatin and paclitaxel-induced STAT3 phosphorylation in OVCAR4 cells (Fig. 9a). Moreover, Momelotinib also reduced paclitaxel-induced expression of TIMP-2 (Fig. 9b), MT1-MMP, MMP-2 (Fig. 9c), the expression of chemoresistance makers ERCC1 and TUBB3 (Fig. 9d) and the CSC markers OCT4 and CD133 (Fig. 9e) strongly indicating that chemotherapeutic induction of these markers requires STAT3 signalling.
In order to explore if paclitaxel-induced P-STAT3 also regulates the expression of TIMP-1 and TIMP-3, mRNA expression of TIMP-1 and TIMP-3 was evaluated on OVCAR4 paclitaxel and Momelotinib treated cells. We demonstrate that besides TIMP-2, paclitaxel significantly enhanced the mRNA expression of TIMP-1 but had no effect on the expression of TIMP-3 (Fig. 9b). However, while the inhibitory effect of Momelotinib was observed on paclitaxel-induced TIMP-2 expression, the expression of TIMP-1 and TIMP-3 remained unaffected (Fig. 9b). These results suggest that chemotherapy induced enhancement in P-STAT3 activation is associated with TIMP-2 and is independent of TIMP-1 and TIMP-3 expression.
There has been a substantial progress in the last few years in understanding the biological role of MMPs and their endogenous tissue inhibitors (TIMPs) in tumour progression [41, 6, 42]. It is now evident that TIMP-2, defined as a tissue inhibitor of MMPs, plays an important regulatory role in tumour biology through both MMP-inhibitory and MMP-independent mechanisms [7, 43, 44]. In this study, we demonstrate that TIMP-2 expression in high-grade serous ovarian tumours is significantly higher than in benign tumours of the same origin. We also demonstrate for the first time that suppression of TIMP-2 expression in Fallopian tube secretory epithelial cells and two ovarian cancer cell lines by an in vitro transient knock down (siRNA) modulates ovarian cell proliferation, invasion and sensitivity to chemotherapy.
The expression of TIMP-2 coincided mostly with the expression of CA125 in high-grade serous tumours, indicating that TIMP-2 is mainly expressed by epithelial tumour cells. However, some diffuse stromal staining of TIMP-2 was also evident in some malignant tumours. In benign tumours, weak expression of TIMP-2 was confined to the ovarian surface epithelium. Previous reports on the expression of TIMP-2 in ovarian tumours and its prognostic impact on the clinical outcome in patients have been ambiguous [45,46,47,48]. These indefinite findings regarding the expression of TIMP-2 in ovarian tumours may be due to different affinities of the antibodies used and differences in the experimental methods used for analysis of the studied protein. Alternatively, it could be due to differences in the pathology of high-grade serous tumours as distinct histopathological and genetically different sub-types of high-grade serous tumours have been described [49, 50].
Since our study demonstrated higher expression of TIMP-2 in high-grade serous ovarian tumours, we used normal secretory Fallopian tube and cancer cell lines that expressed relatively more TIMP-2 than TIMP-1 or TIMP-3, to investigate in vitro the cellular functions of TIMP-2 by transient knockdown. We transiently suppressed the TIMP-2 expression by siRNA in a Fallopian tube secretory epithelial cell line, FT282, and two ovarian cancer cell lines, JHOS2 and OVCAR4. Suppression of TIMP-2 in vitro in the three cell lines was associated with an increase in MT1-MMP expression but inhibition of MMP-2 expression and enzyme activation. Enhanced expression of MT1-MMP and the loss of expression and activation of MMP-2 in response to suppression of TIMP-2 may result due to unavailability of TIMP-2 to bind to MT1-MMP to initiate the activation MMP-2.
We also report for the first time that the suppression of TIMP-2 in ovarian cancer cell lines is associated with a loss of E-Cad mRNA expression with a corresponding increase in the mRNA expression of N-Cad, VIM and a decrease in the mRNA expression of COL12A1. These results are consistent with the study in a non-small cell lung cancer model which showed that overexpression of TIMP-2 upregulated E-Cad expression in in vitro and in vivo models, contributing to the maintenance of cell-cell adhesion and inhibition of tumour growth [44, 51]. Another study using gastric carcinoma cells has shown an inverse relationship between MT1-MMP expression and E-Cad expression, where knock down of MT1-MMP resulted in increased E-Cad expression which was related to inhibition of proliferation and invasion of gastric cancer cells . The loss of E-Cad expression in response to suppression of TIMP-2 expression in ovarian cancer cells in our study did not lead to a change in the expression of classical EMT transcription factors downstream of E-Cad such as SLUG, SNAIL and TWIST. However, a decrease in COL12A1 (alpha chain of type XII collagen, associated with type I collagen) mRNA expression in response to TIMP-2 suppression may be correlated with increased expression of MT1-MMP, a potent protease involved with the degradation of ECM-related fibrillar collagen implicated in tissue remodelling . In this context, it should be mentioned that the mesothelial layer of the peritoneum is rich in interstitial collagen that provides structural support for optimum tissue assembly and hinders foreign implantation . MT1-MMP is also essential for the release of ovarian cancer cells (either as sheets of cells or single cells) from primary tumours, which later accumulate as multicellular aggregates in the peritoneum prior to attachment on the mesothelial lining of the peritoneum . MT1-MMP also promotes migration, cell-matrix detachment, ECM invasion, angiogenesis, formation of multicellular aggregates and growth in three-dimensional collagen matrices in ovarian cancer cells . In addition, active MT1-MMP facilitates the shedding of ectodomain of MUC16/CA125 in ovarian cancer which restrains adhesion and invasion of cancer cells to the peritoneum . These MT1-MMP-mediated functions may explain the enhanced invasion observed in the ovarian cancer cell lines with decreased TIMP-2 expression after siRNA treatment. Enhanced proliferation in response to TIMP-2 suppression may result due to enhancement in the expression of cell cycle analogues CDC25B and CDC25C, which may drive cells through G2 and M phases . However, in the FT282 cell line, knockdown of TIMP-2 may only enhance the M2 phase of the cell cycle through CDC25B. This indicates that TIMP-2 may mediate proliferation in FT282 and ovarian cancer cell lines through different cell cycle mediated mechanisms.
Enhanced proliferation and invasion by knockdown of TIMP-2 in ovarian cancer cell lines is consistent with previous studies that have shown that overexpression of TIMP-2 reduced invasion and proliferation in cells. In melanoma B16F10 cell line TIMP-2 overexpression reduced invasion and angiogenic abilities of these cells . Overexpression of TIMP-2 in rat smooth muscle cells produced a dose-dependent reduction in proliferation . Consistent with that study, silencing miR939 produced an overexpression of endogenous TIMP-2 with consequent significant loss of proliferation of non-small cell lung cancer cell line (NSCLC) .
We have previously reported that both paclitaxel and cisplatin, standard chemotherapies used for the treatment of ovarian cancer patients, promotes an increase in the expression of the chemoresistant markers ERCC1 and TUBB3 and the CSC markers CD44, CD133, OCT4A and EpCAM in ovarian cancer cells, [16, 18, 19, 60]. In this study, we report similar findings in OVCAR4 cells. The increase in chemoresistance and CSC marker expression coincided with the upregulation of TIMP-2 expression and overlapped with the activation of STAT3 pathway in Cont OVCAR4 cells. However, T2-KD OVCAR4 cells, which had reduced TIMP-2 expression, did not exhibit activation of STAT3 or an increase in the expression of chemoresistance and CSC markers in response to chemotherapy treatments. These results may suggest that TIMP-2 and STAT3 activation are intrinsically associated with chemotherapy resistance in ovarian cancer. It can be speculated that the extracellular microenvironment initiated by the cytotoxic damage of the cancer cells may be associated with the activation of STAT3. In this context, the synthesis and secretion of cytokines like interleukin-6 (IL-6), a potent STAT3 activator, have been reported in response to cytotoxic damage in cancer cells . In addition, the concentration of IL-6 increases after platinum treatment of ovarian tumours, and IL-6 secreted by stromal fibroblasts activates STAT3 and enriches the numbers of ALDH+ CSCs in residual tumours . To date, no study has provided a drect link between TIMP-2, STAT3 and chemoresistance. However, a recent paper has demonstrated TIMP-1 mediated chemoresistance in a non-small cell lung carcinoma model via induction of IL-6 secretion . In addition, in vitro TIMP-1 production in primary mouse hepatocytes was enhanced by IL-6 treatment, but it was less in STAT3-deficient hepatocytes .
Accumulating data suggests that the chemotherapy treated tumours facilitate the selection of therapy-resistant CSCs through elimination of sensitive cells, which makes the residual recurrent tumour aggressive and resistant to therapy [16, 64]. In addition, chemotherapy labile apoptotic/necrotic cells release intracellular metabolites and soluble cytokines/chemokines and growth factors which therapy-resistant cancer cells may require for the re-growth and establishment of recurrent tumours [4, 65, 66]. Furthermore, CSCs may escape host immune surveillance by upregulating checkpoint regulators . The embryonic stem cell marker Nanog interacts with the cancer stem cell marker CD44 to activate the STAT3 pathway in ovarian cancer cells . An enhanced expression of STAT3 has been reported in recurrent ovarian tumours extracted from metastatic ovarian lesions and ascites-derived tumours, compared to primary tumours and chemonaive ascites-derived tumours [69, 70]. The genomic and proteomic signatures of recurrent ovarian tumours have been associated with CSCs [21, 69]. Analyses of clinical samples have shown that the expression of CSC markers (CD44, CD133 and ALDH1A) is low in primary tumours but is enhanced in tumours immediately after chemotherapy treatment but reduces back to their original levels at recurrence, suggesting that the initial expression of CSCs markers identifies chemoresistant cells . Our recent study has shown that daily oral treatment with Momelotinib (a potent JAK2/STAT3 inhibitor) as a maintenance treatment in conjunction with chemotherapy suppresses STAT3 activation, the CSC traits, and extends the disease-free period by deterring peritoneal spread in a mouse model of ovarian cancer . Our current study also highlights the important role of the activated STAT3 pathway in CSC-mediated chemoresistance whereby we show a lack of an active STAT3-associated CSC pathway in T2-KD cells.
We report that a STAT3 inhibitor, Momelotinib, inhibits P-STAT3 activation in parental OVCAR4 cells resulting in loss of paclitaxel-induced TIMP-2 upregulation and concomitant loss in the enhancement of the expression of chemoresistance and CSC markers. Although paclitaxel enhanced TIMP-1 expression on parental OVCAR4 cells, Momelotinib had no effect on its expression, strongly suggesting that TIMP-2 mediated chemotherapy-induced STAT3 activation is essential for chemoresistant and CSC phenotypes in ovarian cancer.
TIMPs are secreted by normal and tumour cells and most likely have paracrine effects on the cells in the cellular microenvironment. It is possible that high expression of TIMP-2 in tumours is a pre-requisite for constitutive activation of STAT3 in many cancers or vice versa, constitutive activation of STAT3 may sustain enhanced TIMP-2 expression in certain cancers. In that context, we have demonstrated persistent activation of STAT3 in advanced-stage ovarian cancer . Nuclear existence of activated (phosphorylated) STAT3 has been observed in 70% of advanced-stage ovarian cancer and that has been associated with decreased survival . Whether this persistent STAT3 activation is responsible for enhanced expression of TIMP-2 in ovarian tumours or enhanced expression of TIMP-2 drives constitutive STAT3 activation remains to be determined. In the chemotherapy treatment scenario, it is possible that the chemotherapy-induced acute secretory process, which causes the release of soluble factors (including TIMP-2), may control the activation of STAT3 in ovarian cancer cells. In T2-KD OVCAR4 cells, this aspect of the secretory process may have been compromised resulting in the inability of the cells to activate the STAT3 pathway resulting in the loss of a chemoresistant population. This suggested role of TIMP-2 requires further investigation.
The data from this study indicates opposing roles of TIMP-2 in ovarian tumourigenesis. In the first instance, we show that knock down of TIMP-2 in ovarian cancer cells results in enhanced proliferation and invasion, processes essential for the progression of cancer. However, we also demonstrate that knock down of TIMP-2 enhances the chemosensitivity of ovarian cancer cells, a process that potentially contradicts processes involved with tumourigenesis. We propose that the growth and invasive functions of TIMP-2 in ovarian tumour biology in vitro is MMP-dependent and are regulated by MT1-MMP, while the chemosensitivity aspect may be dependent on chemotherapy-induced activation of the STAT3 pathway. However, as both TIMP-2 and STAT3 are overexpressed in ovarian tumours, activated STAT3 and high TIMP-2 expression may play a dual role in maintaining in vivo ovarian tumourigenesis. Targeting the TIMP-2/STAT3 axis may provide a novel strategy to enhance the efficacy of current chemotherapy regimens, resulting in a much-needed better clinical outcome for this lethal disease. Based on our results, a proposed model of TIMP-2 regulating ovarian cancer proliferation, invasion and chemotherapy-induced chemoresistance is described in Fig. 10.
Availability of data and materials
The data presented in the study are not publicly available as it is a part of a PhD dissertation still in progress. However, the data can be made available from the corresponding author on a reasonable request.
Tissue inhibitor of metalloproteinases
High grade serous ovarian carcinoma
TIMP-2 knocked down cells
Small interfering RNA
Scrambled vector transfected control cells
- P :
Parental cells treated with transfection reagent
- Unt :
Membrane type 1 metalloproteinase
Cancer stem cells
Janus activated kinase
Signal transducer and activator of transcription 3
Excision repair cross-complementation group 1
Tubulin beta 3 class III
Epithelial cell adhesion molecule
Epithelial mesenchymal transition
Sodium dodecyl sulfate-polyacrylamide gel electrophoresis
Quantitative Reverse Transcription Polymerase Chain Reaction
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This work was made possible through the Victorian State Government Operational Infrastructure Support to the Hudson Institute of Medical Research.
This work was supported by the John Turner Cancer Research Funds to Fiona Elsey Cancer Research Institute, Ballarat, Australia. NA is supported by John Turner Cancer Research Funds; RME is a recipient of Australian postgraduate award. MB is supported by Ovarian Cancer Research Foundation, Australia.
Ethics approval and consent to participate
This study was approved by the Research and Ethics Committee of Royal Women’s Hospital (Approval#09/09), Melbourne, Australia. Human ovarian tumour samples were acquired from patients after obtaining written patient information consent as indicated in the Ethics Approval (09/09).
Consent for publication
All authors have seen the contents in the manuscript and agree for its publication. The authors also agree with the order of authorship in the manuscript.
The authors declare no competing interest.
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Figure S3. Reduction of TIMP-2 by siRNA. TIMP-2 was knocked down by predesigned three 27mer small interfering RNA (siRNA A, B, C) duplexes and a pooled siRNA (ABC) directed against TIMP-2 in FT282, JOSH-2 and OVCAR4 cell lines as described in the Methods. (A) mRNA expression of TIMP-2, (B-C) TIMP-1 and 3 was determined by qRT-PCR as described in Methods. Each experiment was repeated three times and was performed in triplicate. Significance was determined by one-way ANOVA *p > 0.05; **p > 0.01; ***p > 0.001; ****p < 0.0001.
Effect of TIMP-2 knock down on the expression of SLUG, SNAIL and TWIST in FT282 and ovarian cancer cell lines. The mRNA expression of SLUG, SNAIL and TWIST in FT282, JHOS2 and OVCAR4 cell lines was evaluated by qRT-PCR. The experiment was repeated three times in triplicate. Error bars are presented as mean ± of SEM.
Quantification of EdU staining in Cont, P and T2-KD FT282, JOSH2 and OVCAR4 cells. Cells were stained with EdU and PI as described in the Methods. Flow cytometer representation of percentage of EdU stained cells in S-phase of the cell cycle.
Microscope filters used for the Immunofluorescence study
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Escalona, R.M., Bilandzic, M., Western, P. et al. TIMP-2 regulates proliferation, invasion and STAT3-mediated cancer stem cell-dependent chemoresistance in ovarian cancer cells. BMC Cancer 20, 960 (2020). https://doi.org/10.1186/s12885-020-07274-6
- Ovarian cancer
- Cancer stem cells