Abstract:Objective: To ide.pngy the expression of ubiquitin specific peptidase 3 (USP3) in bladder cancer and explore the possibility of USP3 serving as a prognostic marker for bladder cancer. Methods: Oncomine database was used to compare the expression of USP3 between bladder cancer and normal tissues. Furthermore, we further confirmed the USP3 expression in bladder cancer through detecting the USP3 level in our bladder cancer tissues and adjacent tissues of cancer as well as in bladder cancer cell lines and normal urothelial cell line using immunohistochemistry, qRT-PCR and Western blotting. Then we used TCGA database to analyze the relationship between the expression of USP3 and the prognosis of bladder cancer patients. Finally, USP3 association networks were predicted by STRING database and The analysis of gene ontology enrichment and KEGG Pathway was performed on the USP3 interaction proteins were. Results: All the analyses in Oncomine demonstrated that the level of USP3 was higher in the bladder cancer tissues than in normal tissues (P<0.05). The results of immunohistochemistry and qRT-PCR te.pngied that the protein and mRNA levels of USP3 were significantly overexpressed in bladder cancer tissues as compared with those in adjacent tissues of cancer (P<0.05). At the cellular level, the results of Western blotting and qRT-PCR also illustrated that the protein and mRNA levels of USP3 in two bladder cancer cell lines were significantly higher than in the normal urothelial cell line SV-HUC-1 (P<0.05). The survival analyses through the TCGA database revealed that high transcription levels of USP3 were associated with poorer overall survival in bladder cancer patients (P<0.05), but not with recurrence (P>0.05). Ten USP3-interacting proteins were predicted by the STRING database and the GO analysis revealed that these proteins were enriched in many biological processes, such as histone deubiquitination, chromatin organization and histone modification. They also participated in systemic lupus erythematosus, alcoholism, viral carcinogenesis and basal transcription factors. Conclusions: USP3 is up-regulated in bladder cancer and is closely associated with prognosis, suggesting USP3 may participate in bladder cancer progression. USP3 is valuable to be a prognostic marker of bladder cancer.
[1] Chen W, Zheng R, Baade PD, et al. Cancer statistics in China, 2015. CA Cancer J Clin, 2016,66(2):115-132.
[2] 李秀宁,高超,刘翰楠,等.膀胱癌转移机制的生物信息学研究.医学信息,2015,16(18):10.
[3] 李飞,梁中锟,荆玉明,等.基于BRB-ArrayTools和GATHER工具对膀胱癌相关基因的挖掘及生物信息学分析.临床泌尿外科杂志,2011,26(11):852-855.
[4] Sloper-Mould KE, Eyre HJ, Wang XW, et al. Characterization and chromosomal localization of USP3, a novel human ubiquitin-specific protease. J Biol Chem, 1999,274(38):26878-26884.
[5] Nicassio F, Corrado N, Vissers JH, et al. Human USP3 is a chromatin modifier required for S phase progression and genome stability. Curr Biol, 2007,17(22):1972-1977.
[6] Wang ZZ, Yang J, Di JB, et al. Downregulated USP3 mRNA functions as a competitive endogenous RNA of SMAD4 by sponging miR-224 and promotes metastasis in colorectal cancer. Sci Rep, 2017,7(1):4281.
[7] Fu S, Shao SZ, Wang LQ, et al. USP3 stabilizes p53 protein through its deubiquitinase activity. Biochem Biophys Res Commun, 2017,492(2):178-183.
[8] Fuchs SY. The role of ubiquitin-proteasome pathway in oncogenic signaling. Cancer Biol Ther, 2002,1(4):337-341.
[9] Haas AL, Siepmann TJ. Pathways of ubiquitin conjugation. FASEB J, 1997,11(14):1257-1268.
[10] Sharma N, Zhu QZ, Wani G, et al. USP3 counteracts RNF168 via deubiquitinating H2A and gamma H2AX at lysine 13 and 15. Cell Cycle, 2014,13(1):106-114.
[11] 周晓华,张蓬波,张秀忠,等.泛素特异肽酶9与肿瘤的研究进展.中国肿瘤外科杂志,2017,9(4):261-263.
[12] 庄雅靖,廖志伟,喻芳,等.泛素特异性肽酶22基因与肿瘤发展和预后的研究进展.国际医药卫生导报,2014,20(17):2627-2631.