Tumour suppressor OTUD3 induces growth inhibition and apoptosis by directly deubiquitinating and stabilizing p53 in invasive breast carcinoma cells

Background P53 pathway inactivation plays an important role in the process of breast cancer tumourigenesis. Post-translational protein modification abnormalities have been confirmed to be an important mechanism underlying the inactivation of p53. Numerous deubiquitinating enzymes are aberrantly expressed in breast cancer, and a few deubiquitination enzymes are capable of deubiquitinating and stabilizing p53. Here, we report that OTUD3 is a deubiquitylase of p53 in breast carcinoma. Methods The correlation between the mRNA expression of OTUD3, TP53 and PTEN and the prognosis of BC was assessed with the Kaplan-Meier Plotter tool. OTUD3 protein expression in breast carcinoma was examined by immunohistochemistry and western blotting. The relationship among OTUD3, p53, and p21 proteins was analysed. Half-life analysis and ubiquitylation assay were performed to elucidate the molecular mechanism by which OTUD3 stabilizes p53. The interaction between OTUD3 and p53 in BC cells was verified by a co-immunoprecipitation assay and GST pulldown experiments. MTS proliferation detection, an apoptosis detection kit and colony formation asssy were used to investigate the functional effects of OTUD3 on breast cancer cells. Results OTUD3 downregulation is correlated with a poor prognosis in BC patients. OTUD3 expression is decreased in breast cancer tissues and independent of the histological grade.OTUD3 also inhibits cell proliferation and clone formation and increases the sensitivity of BC cells to apoptosis induced by chemotherapy drugs. A reduction in OTUD3 expression concomitant with decreased p53 abundance is correlated with human breast cancer progression. The ectopic expression of wild-type OTUD3, but not its catalytically inactive mutant, stabilizes and activates p53. Mechanistically, OTUD3 interacts directly with p53 through the amino-terminal OTU region. Finally, OTUD3 protects p53 from Mdm2-mediated ubiquitination and degradation, enabling the deubiquitination of p53 in BC cells. Conclusions summary, restoring in breast cancer cells and suggest that the OTUD3-p53 signalling axis plays a critical role in suppression. and

Results OTUD3 downregulation is correlated with a poor prognosis in BC patients. OTUD3 expression is decreased in breast cancer tissues and independent of the histological grade.OTUD3 also inhibits cell proliferation and clone formation and increases the sensitivity of BC cells to apoptosis induced by chemotherapy drugs. A reduction in OTUD3 expression concomitant with decreased p53 abundance is correlated with human breast cancer progression. The ectopic expression of wild-type OTUD3, but not its catalytically inactive mutant, stabilizes and activates p53. Mechanistically, OTUD3 interacts directly with p53 through the amino-terminal OTU region. Finally, OTUD3 protects p53 from Mdm2mediated ubiquitination and degradation, enabling the deubiquitination of p53 in BC cells.
Conclusions In summary, we establish that OTUD3 is a potential therapeutic target for restoring p53 function in breast cancer cells and suggest that the OTUD3-p53 signalling axis plays a critical role in tumour suppression. Background 3 Invasive breast carcinoma (BC) is the leading cause of all new cancer diagnoses in women [1].
Tumour protein p53 pathway inactivation plays an important role in the process of BC tumour genesis. Wild-type p53 is present in approximately 70% of BC cases [2], and the p53 pathway is partially abrogated through the inactivation of various signal or effector elements [3]. Accordingly, the role of p53 signalling in BC tumour genesis has attracted much attention [4]. In addition to point mutations and gene deletions, post-translational protein modification abnormalities have been confirmed to be an important mechanism underlying the inactivation of p53. Among these abnormalities, ubiquitination is more complex than phosphorylation and acetylation [5]. Most research focuses on the regulatory effect of ubiquitin ligase on the ubiquitination of p53 [6]; this research includes the well-known ubiquitination enzyme Mdm2 [7,8]. Recently, the N-terminal p53 TAD and Mdm2 pBD regions were studied to discover anticancer drug molecules [4]. However, limited success was achieved due to tumour recurrence [9] or TP53 gene mutations [10]. The intriguing nature of the regulation of p53 signalling and its role in tumourigenesis are certainly puzzling due to the complexity involved [4]. Therefore, it is particularly important to identify more ways to stabilize p53.
The ubiquitination of many proteins has been well documented to be reversed by deubiquitinating enzymes (DUBs), which belong to a superfamily of cysteine proteases and metalloproteases that cleave ubiquitin-protein bonds. The human genome encodes approximately 100 DUBs [11] that can be classified into the following six families: ubiquitin-specific proteases (USPs), ubiquitin car boxy- In BC, numerous DUBs [11], including breast cancer-promoting DUBs and cancer-suppressing DUBs are aberrantly expressed. However, only two deubiquitination enzymes are capable of deubiquitinating and stabilizing p53 [11].USP7 (HAUSP) might represent the first example [12].
However, TSPYL5 can bind USP7 and suppress its ability to deubiquitinate and stabilize p53 [13]. In addition, an interesting feedback loop exists in p53 regulation because USP7 also binds, 4 deubiquitinates and stabilizes Mdm2 more potently under physiologic conditions [14,15] and stabilizes p53 under genotoxic stress conditions [16,17]. USP10 can deubiquitinate cytoplasmic p53 and inhibit MDM-2-mediated p53 nuclear export and degradation. USP10 can also shuttle into the nucleus and stabilize p53 when DNA damage occurs [18]. However, USP10 may stabilize both wildtype p53 and mutant p53 [19] and is more highly expressed in breast cancer tissue than adjacent normal tissue [20]. Unsurprisingly, such an important tumour suppressor is controlled by multiple DUBs. However, few DUBs have been found in breast cancer, and the mechanisms regulating p53 deubiquitination remain enigmatic.
Our previous study found that OTU deubiquitinase 3 (OTUD3) can deubiquitinate and stabilizes PTEN [21]. In the current study, we found that the expression of OTUD3 was decreased in BC and proved for the first time that OTUD3 is an enzyme related to the deubiquitination of p53. Compared with PTEN, the high expression levels of OTUD3 and p53 are more indicative of a better prognosis in BC. This study further elucidated the influence of OTUD3 on BC cell biological function and its molecular mechanism and suggests that OTUD3 should be explored as a therapeutic target in breast cancer.

Kaplan-Meier Plotter
The correlation between the mRNA expression of OTUD3, TP53 and PTEN and the prognosis of BC was assessed with the Kaplan-Meier Plotter tool [22,23] (http://kmplot.com/analysis/index). BC patients were divided into two groups according to the median expression (high expression vs. low expression). A Kaplan-Meier survival chart was used in the analysis to evaluate the relapse-free survival (RFS) of the patients, and the risk ratio (HR) with its 95% confidence interval (CI) and logrank test were used to calculate the p-value.

Antibodies and reagents
An anti-OTUD3 antibody (HPA028544) for immunohistochemistry (IHC) and the proteasome inhibitor MG132 were purchased from Sigma-Aldrich, USA. An anti-OTUD3 antibody (ab107646), wild-type anti-p53 antibody (ab131442), and anti-p21 antibody (ab109520) for western blotting were purchased from Abcam, United Kingdom. An anti-glyceraldehyde 3-phosphate dehydrogenase (anti-GAPDH) and secondary antibodies were purchased from Santa Cruz Biotechnology, Inc., USA. The anti-Myc and anti-Flag antibodies were obtained from MBL BEIJING B&M BIO TECH CO.,LTD, Beijing China.

Immunohistochemistry
Immunohistochemistry was performed by using the avidin-biotin complex method, including heatinduced antigen-retrieval procedures. The incubation with an antibody against OTUD3 (1:100 dilution; HPA028544) was carried out at 4°C for 18 h. All staining was assessed by a quantitative imaging method (inForm, PerkinElmer) utilizing continuous measurement and pathologists blinded to the sample origins and subject outcomes. The widely accepted German semi-quantitative scoring system based on the staining intensity and area was used. Each specimen was assigned a score according to the intensity of the nuclear, cytoplasmic, and/or membrane staining (no staining=0; weak staining=1, moderate staining=2, and strong staining=3) and the extent of the stained cells (0%=0, 1-24%=1, 25=49%=2, 50-74%=3, and 75-100%=4). The final immunoreactive score was determined by multiplying the intensity score by the extent score, and this value ranged from 0 (minimum) to 12 (maximum).

Western blot analysis
The cells and tissue specimens were lysed using RIPA buffer (Sigma-Aldrich, St. Louis, MO, USA). The protein samples were separated using 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and transferred onto PVDF membranes (Millipore). The membranes were blocked with 5% non-fat milk at room temperature for 2 h and incubated overnight with primary antibodies at 4°C. After washing with TBST three times for 15 min each, the membranes were incubated with the appropriate horseradish peroxidase-conjugated secondary antibodies for 2 h at room temperature with slight shaking. GAPDH was used as the loading control. The immunoreactive bands were visualized using SuperSignal West Pico Chemiluminescent Substrates (Thermo, USA).

Protein half-life assay
For the p53 half-life assay, the MCF7 and DU4475 cells were grown in 2-cm plates to approximately 60% confluence, and then, the cells were transfected with OTUD3 shRNAs. After twenty-four hours, the cells were treated with the protein synthesis inhibitor cycloheximide (CHX, Sigma, 10 µg ml-1) for the indicated durations before collection.

Immunoprecipitation
The cultured cells were lysed with HEPES lysis buffer (20 mM HEPES, pH 7.2, 50 mM NaCl, 0.5% Triton X-100, 1 mM NaF and 1 mM dithiothreitol) supplemented with Protease Inhibitor Cocktail Tablets (Roche). The immunoprecipitations were performed using the indicated primary antibody and protein A/G agarose beads (Santa Cruz) at 4°C. Then, the immunocomplexes were washed with HEPES lysis buffer four times. Both the lysates and immunoprecipitates were examined using the indicated primary antibodies, followed by incubation with the appropriate secondary antibody and SuperSignal 7 West Pico Chemiluminescent Substrate (Thermo).

GST pulldown assays
Bacterial-expressed GST and GST-p53 bound to glutathione-Sepharose 4B beads (from GE) were incubated with Myc-OTUD3-expressing MCF7 cells for 2 h at 4°C. Then, the beads were washed with GST binding buffer (100 mM NaCl, 10 mM Tris,50 mM NaF, 2 mM EDTA, 0.5 mM Na 3 VO 4 and 1% Nonidet P40) four times, and the proteins were eluted and subjected to western blotting.

Ubiquitylation assay
The cells were treated with 20 mM MG132 proteasome inhibitor for 8 h. Then, the cells were washed with PBS and lysed in 0.5 ml of HEPES buffer (20 mM HEPES, pH 7.2, 50 mM NaCl, 1 mM NaF, and 0.5% Triton X 100) supplemented with 0.1% SDS and a protease inhibitor cocktail (Roche, Germany).
The lysates were centrifuged to obtain the cytosolic proteins. Briefly, the individual samples were incubated with primary antibodies for 3 h, followed by incubation with protein A/G agarose beads (Santa Cruz) for another 8 h at 4°C. The beads were washed three times with HEPES buffer. The proteins were released from the beads by boiling in 40 ml of 26SDS-PAGE sample buffer for 10 min.
The samples were subjected to a western blot analysis.

Colony formation assays
The cells were resuspended in DMEM containing 0.35% low-melting agarose (Sigma) and 10% FBS and seeded onto a coating of 0.7% low-melting agarose in DMEM containing 10% FBS. The plates were incubated at 37°C and 5% CO 2 , and the colonies were scored 3 weeks after preparation.
Colonies larger than 0.1 mm in diameter were scored as positive.

Statistical analysis
The difference between two independent groups was evaluated using unpaired Student's t-test. Chisquare tests and one-way ANOVA were used to compare the groups. A correlation analysis was performed by Spearman's rank correlation coefficient. All IHC and WB statistical analyses were performed with GraphPad Prism 7.00 and SPSS 19.0(IBM Corp, USA). All other results are expressed as the mean±standard deviation (SD) of three independent experiments unless stated otherwise. All statistical tests were two-sided, and P-values<0.05 (*) or <0.01 (**) were considered statistically significant.

High OTUD3 expression is down-regulated in BC tissues and associates with a better prognosis in BC patients
OTUD3 is not frequently mutated in the TCGA pan-cancer dataset (https://www.cbioportal.org/). To assess OTUD3 expression in BC patients, we first analysed the gene expression UALCAN [24] (datasetshttp://ualcan.path.uab.edu/)of human BC. The results showed that the OTUD3 mRNA levels in the BC tissues were significantly lower than those in normal breast tissues (Fig. 1A). The OTUD3 mRNA levels were not associated with the individual cancer stages (Fig. 1B). Although there were no differences in the OTUD3 mRNA levels between the luminal samples and HER2-positive or triplenegative BC samples, there was a difference in the OTUD3 mRNA levels between the HER2-positive and triple-negative BC samples (Fig. 1C). We used data obtained from the cBioPortal database [25,26] (https://www.cbioportal.org/)and found that decreases in OTUD3 mRNA levels may not be due to increased OTUD3 DNA methylation in BC (Fig. 1D).
Our previous results showed that OTUD3 could deubiquitinate and stabilize PTEN. Here,we want to find whether OTUD3 is an enzyme related to p53.Therefore, we performed a Kaplan-Meier survival analysis [22,23] (http://kmplot.com/analysis/index) to evaluate the association between OTUD3, TP53 and PTEN expression and survival in BC patients firstly. Interestingly, the RFS Recurrence-free survival rate in the high OTUD3 expression group (n=1986) was better than that in the low OTUD3 expression group (n=1965), p=0.00034 (Fig. 1 E). Similarly, the patients with high TP53 (n=1977) expression suffered a better RFS than the patients in the low expression group (n=1974), p=0.00054 (Fig. 1F). However, the expression level of PTEN was not an independent prognostic factor in the BC patients in the data set, p=0.62 (Fig. 1G). We speculate that high OTUD3 expression is associated with a better prognosis in BC patients and that the relationship between OTUD3 and p53 is the most significant.

OTUD3 expression is downregulated in BC tissue
Consistent with the OTUD3 mRNA results, the protein expression level of OTUD3 was also significantly lower in the BC tissue than the normal breast tissue. Immunohistochemical (IHC) staining with an anti-OTUD3 antibody was performed on 80 pairs of BC tissues and adjacent non-tumour tissues. Staining scores of 0-6 were considered negative, and scores of 6-12 were considered positive. As shown in Fig Notably, OTUD3 expression in the breast cancer tissue was not associated with the molecular type (χ =2.672,p=0.614) (Fig. 2B). Even if not statistically significant, there is a trend that OTUD3 may be down-regulated in luminal B (Her-2-positive) compared with adjacent tissue.
The half-life of the wild-type p53 protein is very short, and the p53 protein detected by IHC in various experiments is the mutant p53 protein [28,29]. Therefore, we analysed the expression of p53 and OTUD3 in 26 pairs of fresh and frozen BC tissues and adjacent normal tissue by WB. The expression of the p53 downstream protein p21 was also detected. P21 WAP1/cip1 is a p53-induced cell cycle kinase inhibitor (CDKI) [30]. P53 causes G1 cell arrest by regulating the expression of p21 [31].The knockout of p21 results in the complete loss of p53-mediated human tumour cell cycle (G1) arrest [32].The specimens were numbered by the date of collection and grouped by histological grade. Our experimental results prove for the first time that OTUD3 and p53 are both expressed in breast cancer and adjacent normal tissues.
Notably, the expression of OTUD3 p=0.0069 and p53(p=0.041) in all BC tissues was lower than that in the corresponding normal tissues (Fig. 2C). OTUD3 expression in the breast cancer tissue was independent of the histological grade (F=1.736, p=0.199) (Fig. 2D).Additionally, the analysis of the relationship between OTUD3 expression and p53 expression showed a significantly positive correlation (r=0.8849, 95% CI: 0.8068-0.9326, p<0.0001), and the levels of OTUD3 and p21 were also positively correlated (r=0.6427, 95% CI: 0.4484-0.779, p<0.0001) (Fig. 2E). Our clinical data fully proved that OTUD3 is downregulated in cancer tissues and is highly correlated with p53 expression.

OTUD3 maintains p53 stability in vitro
Since the expression levels of OTUD3 and p53 are correlated we tested whether the overexpression of OTUD3 affects p53 protein levels in breast cancer cells. Two well-established p53 target genes, p21 and the proapoptotic gene BCl-2-associated X protein (BAX), were assayed to reflect p53 activity.
Here, we used the luminal breast cancer cell line MCF7 and the TNBC cell line DU4475, both of which express wild-type p53 [33]. As shown in Fig. 3A, the p53 level was dramatically increased when OTUD3 was overexpressed in the MCF7 cells and DU4475 cells; increased p21 and BAX protein levels were also observed, indicating that OTUD3 also activates p53-dependent transcriptional activation. To confirm the role of OTUD3 in the regulation of p53, the MCF7 and DU4475 cells were transfected with sh-ctrl or sh-OTUD3 lentivirus. The changes in the p53 protein level were determined. We found that the OTUD3 knockdown in the BC cells resulted in a dramatic decrease in the protein level of endogenous p53 accompanied by a decrease in the two target genes (Fig. 3B). To test the possibility that OTUD3 regulation of p53 occurs through the modulation of p53 protein stability, we treated cells stably expressing OTUD3 shRNA with the proteasome inhibitor MG132 (20 µM, 8 h). The decrease in the p53 levels was reversed by the MG132 treatment (Fig. 3B). This finding suggests that OTUD3 regulates p53 levels by increasing its stability in a proteasome-dependent manner.
Ubiquitin-mediated degradation is the only way by which p53 is terminated by the proteasome [34].
To date, some p53 E3 ligases have been found, and MDM2 is the most important [35]. MDM2 (murine double minute 2, human HDM2) is an oncogene that promotes cell division and proliferation [36].
MDM2 mediates the sustainable degradation of most p53 proteins, resulting in a very low p53 intracellular level [37].P53 is regulated by Mdm2-mediated ubiquitination and degradation and has a short half-life (5-20 min) [38]. Subsequently, we examined the half-life of p53 in the absence or presence of OTUD3. We treated the control cells and cells stably expressing OTUD3 shRNA with or without OTUD3 overexpression with the protein synthesis inhibitor cycloheximide (CHX) and examined the p53 levels at various time points. The half-life of endogenous p53 was significantly shortened in the BC cells depleted of OTUD3, and this effect was fully reversed by the ectopic expression of OTUD3 (Fig. 3C). OTUD3 likely deubiquitinates p53 to counteract the action of the E3 ubiquitin ligase Mdm2. Indeed, as shown in Fig. 3D, ectopic Mdm2 expression significantly induced p53 degradation, while the coexpression of OTUD3 efficiently rescued p53 from Mdm2-induced degradation. These results demonstrate that OTUD3 can antagonize the reduction in p53 by Mdm2.

OTUD3 interacts with p53
Co-immunoprecipitation (CO-IP) assays were conducted in MCF7 cells and DU4475 cells to examine whether OTUD3 physically interacts with p53. As shown in Fig. 4A, endogenous OTUD3 was specifically co-immunoprecipitated with endogenous p53 in the cells by anti-p53 antibodies.
Furthermore, p53 co-immunoprecipitated with endogenous OTUD3 in the MCF7 cells and DU4475 cells (Fig. 4B). Then, we constructed OTUD3 truncated mutants as follows: OTUD3 was divided into two parts per its domain structure, namely, D1 (1-183) containing the OTU domain and D2 (184-398) containing the UBA domain and the C tail (Fig. 4C). Using the D1 and D2 constructs in coimmunoprecipitation experiments, we revealed that the OTU domain-containing region D1 (1-183) is critical for the interaction between OTUD3 and p53 (Fig. 4D). To determine whether the OTUD3-TP53 interaction was direct, we generated and purified recombinant Myc-OTUD3, Myc-D1 and Myc-D2.
Interestingly, Myc-D1 cultured from MCF7 cells was specifically bound by the purified GST-TP53 protein but not GST alone (Fig. 4E). This finding further illustrated the direct interaction between OTUD3 and p53.  4G, H). These results suggest that a direct interaction exists between OTUD3 and p53.

OTUD3 deubiquitinates p53
As OTUD3 is a deubiquitinase, we examined whether OTUD3 deubiquitinates p53. To elucidate the molecular mechanism by which OTUD3 stabilizes p53, we determined whether OTUD3 directly controls the levels of p53 ubiquitination. As indicated in Fig. 5A, a high level of ubiquitinated p53 was found in the MCF7 and DU4475 cells transfected with Mdm2 (lane 2); however, p53 ubiquitination was significantly abrogated by OTUD3 expression (comparison of lanes 3 and 2). Significantly, the enzyme activity of the mutant OTUD3 C76A lost its ability to deubiquitinate p53 (Fig. 5A, lane 4). This finding indicates that p53 stabilization by OTUD3 requires deubiquitinating enzymatic activity. In contrast, the OTUD3 downregulation by shRNA increased p53 ubiquitination in the MCF7 and DU4475 cells (Fig.   5B). Collectively, these data demonstrate that OTUD3 negatively regulates p53 ubiquitination in breast cancer cells and plays an important role in the balance between p53 ubiquitination and deubiquitination. We speculate that the balance between the Mdm2-mediated ubiquitination and OTUD3-mediated deubiquitination of p53 is critical for p53 stabilization.

13
P53 stabilization is crucial for its suppression of cell growth and apoptosis. To investigate the biological role of OTUD3, we first examined its effect on cell proliferation. We compared the proliferation rates of MCF7 and DU4475 cells stably transfected with OTUD3 and OTUD3 C76A with those of negative control cell lines using an MTS proliferation test kit. The results showed that cell proliferation slowed after the OTUD3 transfection and accelerated after the OTUD3 C76A transfection (Fig. 6A). Compared to the control cells, the knockdown of endogenous OTUD3 by shRNA in the MCF7 and DU4475 cells increased the cell proliferation rate. However, the DU4475 cells proliferated at a significantly slower rate after OTUD3 expression was restored. OTUD3 could rescue the accelerated cell proliferation caused by the OTUD3 knockdown, but the enzyme inactive mutant OTUD3 C76A could not inhibit the accelerated cell proliferation, indicating that the regulation of the effect of OTUD3 on cell proliferation depends on its ubiquitinase activity (Fig. 6B). These data suggest that OTUD3 can inhibit BC cell proliferation.

OTUD3 induces apoptosis in BC cells and inhibits colony formation
Chemotherapy is an important method for the treatment of BC. The P53-mediated pathways can be activated by genotoxic compounds, such as cisplatin chemotherapeutic compounds, leading to cell cycle arrest and cell death [39]. We treated BC cells with the chemotherapy drug cisplatin (10 mM, 24 h) and detected apoptosis. The results showed that the OTUD3-transfected cells were significantly more sensitive to cisplatin-induced apoptosis than the negative control cells (p<0.01); however, the sensitivity of the transfected OTUD3 C76A cells was significantly decreased (p<0.01) (Fig. 7A).
Compared with the negative control cells, the decreased OTUD3 protein levels increased the resistance of the tumour cells to cisplatin-induced apoptosis (p<0.01). The apoptosis rate was significantly increased when OTUD3 was restored to the levels of the cells not treated with shRNA (p<0.01), but when the levels of OTUD3 C76A were restored in the cells, the apoptosis rate did not significantly change (Fig. 7B). These results suggest that OTUD3 has a certain response to chemotherapy-induced BC cell apoptosis and that this response depends on its deubiquitinase activity.
14 Subsequently, we examined the effect of OTUD3 on cell growth using a colony formation assay. The BC cells were infected with either a control vector or a vector encoding OTUD3 or OTUD3 C76A and cultured for 2 weeks. Strikingly, OTUD3, but not OTUD3 C76A , strongly inhibited the number of colonies of BC cells (Fig. 7C). When OTUD3 was knocked down, the cell clone formation ability was enhanced, and when OTUD3 was restored, the clone formation ability was inhibited (Fig. 7D). However, the ability of cell cloning was significantly enhanced after the OTUD3 C76A overexpression.

Discussion
Our experiment proved for the first time that OTUD3 is a tumour-suppressing DUB in BC. The online database analysis showed that BC patients with high OTUD3 and p53 expression have a better RFS, thus revealing a potential prognostic biomarker of BC. In addition, the mRNA expression of OTUD3 was lower in the BC tissue compared to normal adjacent tissue and was unrelated to the staging or molecular type. The clinical sample study of the Qilu cohort further proved that the protein expression of OTUD3 in the BC tissues was lower than that in the adjacent tissues. OTUD3 expression in cancer tissues was independent of the molecular type and histological classification. Therefore, the absence of OTUD3 is associated with the occurrence of BC. As a tumour suppressor gene, OTUD3 may serve as a new biomarker of the occurrence and development of BC. Targeting the OTUD3 upstream and downstream pathways could be a useful therapeutic strategy because BC cells may have lost the expression of such tumour-suppressing DUBs.
Functional p53 prevents the progression of cancer by increasing growth inhibition in the form of apoptosis, senescence and/or autophagy [40]. Deubiquitination is a major mechanism that stabilizes p53 and induces apoptosis. The regulation of p53 ubiquitination and deubiquitination in BC is of great interest but remains poorly understood. Our study proves for the first time that the downregulation of OTUD3 in clinical BC samples highly coincides with the downregulation of p53. OTUD3 can directly interact with and stabilize p53 through deubiquitination in BC cells. The N terminal of OTUD3 contains an OTU domain that directly participates in the binding of the T2 and T3 sequences of p53. The decreased OTUD3 expression could be an important mechanism underlying the loss of TP53 function in breast cancer cells carrying WT TP53 alleles. Both breast cancer cell lines used in this study were p53 wild-type BC cells subtype of MCF-7 is luminal BC and DU4475 cell lines is TNBC. The functional experiments using BC cells further confirmed its anticancer function. OTUD3 supplements enzymes that can regulate p53 by deubiquitination and participates in protein-protein interactions in BC. Thus, OTUD3 is of great significance.
The major causes of death from breast cancer are due to relapse, drug-resistance and metastasis, which are highly related to the dysregulation of the mouse double minute (MDM) family [41][42][43] The MDM family comprises the E3 ligase MDM2 and its close homologue MDM4 (alternatively termed MDMX). MDM2 is a vital regulator of tumour suppressor p53 activity in the breast, [7,8,44] and has been identified as an independent prognostic biomarker in BC [45]. The complex between MDM2 and p53 is largely formed by the interaction between the N-terminal domain of MDM2 and the N-terminal transactivation (TA) domain of p53 (residues [15][16][17][18][19][20][21][22][23][24][25][26][27][28][29] [46,47]. The N-terminal domain of p53 contains the main Mdm2 binding site. The finding that OTUD3 potentially binds the N-terminus of p53 could suggest that both Mdm2 and OTUD3 compete for the same binding site in p53, possibly explaining the observed effects of OTUD3 overexpression and knockdown on p53 ubiquitination and p53 levels in cells. This spatially separates MDM2 from p53, resulting in the stabilization of the p53 protein and allowing p53 to regulate gene transcription, leading to p21 and BAX expression, cell cycle arrest, and/or cell death.
We found that OTUD3 deletion is generally associated with the obliteration of WT p53 in BC. This finding suggests that OTUD3 loss may be selected by tumours to disrupt the p53 pathway. Although our findings reveal an important mechanism by which p53 can be stabilized by direct deubiquitination and imply that OTUD3 might function as a tumour suppressor in vivo through the stabilization of p53, many questions remain unanswered. Our study found that the OTUD3 mRNA level was not related to DNA methylation through an online database thus, the reason for the decrease in OTUD3 expression in BC remains to be further explained. In addition, the effect of OTUD3 on other key regulators in the p53 pathway also needs to be examined.

Availability of data and materials:
The datasets generated during the current study are available from the corresponding author on reasonable request.

Ethical approval
All procedures performed in studies involving human participants were in accordance with the ethical standards of the Research Ethics Committee of Qilu Hospital (Qingdao) of Shandong University and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Consent for publication
Not applicable. No individual's data are presented in this article.

Supplementary Files
This is a list of supplementary files associated with this preprint. Click to download.
supplementary information.ppt