Wang Huan, Luo Wenqin, Wang Xuliang, Xue Dingwei, Ren Liangliang, Xu Li, Ge Guangju, Xia Liqun, Yu Shicheng, Wang Mingchao, Zhou Zhenwei, Li Gonghui, Wu Haiyang
Department of Urology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Department of Urology, The Affiliated Hangzhou First People's Hospital of Zhejiang University School of Medicine, Hangzhou, China.
Front Mol Biosci. 2021 Sep 20;8:670409. doi: 10.3389/fmolb.2021.670409. eCollection 2021.
Testicular nuclear receptor 4 (TR4) is a member of the nuclear hormone receptor family and acts as a ligand-activated transcription factor and functions in many biological processes, such as development, cellular differentiation, and homeostasis. Recent studies have shown that TR4 plays an important role in prostate cancer, renal cell carcinoma, and hepatocellular carcinoma; however, its potential link to bladder cancer (BC) remains unknown. This study found that bladder cancer exhibited a higher expression of TR4 compared to normal tissues. Overexpressed TR4 promoted the bladder cancer cell proliferation, and knocked down TR4 with TR4-siRNA suppressed the bladder cancer cell proliferation. Mechanistic studies reveal that TR4 functions by altering the expression of Bcl-2 to regulate apoptosis in bladder cancer cells. Furthermore, knocking down Bcl-2 reversed the BC proliferation induced by TR4. , we also confirmed that TR4 knockdown mice (TR4) showed slower bladder cancer growth than wild-type mice (TR4) induced by the carcinogenic chemicals. Moreover, TR4 mice showed a lower grade of histopathology than the control group. In conclusion, these results indicate that TR4 plays a key role in bladder cancer proliferation, and targeting TR4 would probably be a potential strategy for bladder cancer treatment.
睾丸核受体4(TR4)是核激素受体家族的成员,作为配体激活的转录因子,在许多生物学过程中发挥作用,如发育、细胞分化和体内平衡。最近的研究表明,TR4在前列腺癌、肾细胞癌和肝细胞癌中起重要作用;然而,其与膀胱癌(BC)的潜在联系仍不清楚。本研究发现,与正常组织相比,膀胱癌中TR4的表达更高。过表达的TR4促进膀胱癌细胞增殖,而用TR4-siRNA敲低TR4则抑制膀胱癌细胞增殖。机制研究表明,TR4通过改变Bcl-2的表达来调节膀胱癌细胞的凋亡。此外,敲低Bcl-2可逆转TR4诱导的BC增殖。我们还证实,敲低TR4的小鼠(TR4)比由致癌化学物质诱导的野生型小鼠(TR4)的膀胱癌生长更慢。此外,TR4小鼠的组织病理学分级低于对照组。总之,这些结果表明TR4在膀胱癌增殖中起关键作用,靶向TR4可能是膀胱癌治疗的潜在策略。