Tang Jian, Wang Zheng, Liu Jiahua, Zhou Chao, Chen Jinxian
Department of Gastrointestinal Surgery, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, P.R. China.
Oncol Lett. 2018 Nov;16(5):6100-6108. doi: 10.3892/ol.2018.9351. Epub 2018 Aug 23.
5-hydroxytryptamine receptor 3A () is an important member of the 5-HT family, which has been suggested to contribute to human tumor development. However, the functions of in human cancer, particularly in colorectal carcinoma (CRC) have not been well-characterized. Reverse transcription quantitative polymerase was performed to detect endogenous expression in 6 CRC cell lines. was then knocked down via a lentivirus-mediated shRNA system to detect the effect of silencing on cell proliferation and apoptosis by MTT, colony formation, flow cytometry and western blotting assays in CRC. was expressed at different levels in the 6 CRC cell lines. In addition, knockdown inhibited CRC cell proliferation and colony formation, resulting in cell cycle arrest and the promotion of cell apoptosis. Additionally, the expression levels of apoptosis-associated proteins including BAD and BAX were increased, while Bcl-2 expression was decreased following knockdown. In summary, the data of the present study indicated that serves an important role in colon carcinogenesis, but in-depth studies of the mechanisms underlying these data are required to demonstrate whether it may be used as a novel target for CRC therapy.
5-羟色胺受体3A()是5-羟色胺(5-HT)家族的重要成员,已表明其与人类肿瘤发展有关。然而,其在人类癌症,尤其是在结直肠癌(CRC)中的功能尚未得到充分表征。进行逆转录定量聚合酶反应以检测6种CRC细胞系中的内源性表达。然后通过慢病毒介导的短发夹RNA(shRNA)系统敲低,以通过MTT、集落形成、流式细胞术和蛋白质印迹分析检测沉默对CRC细胞增殖和凋亡的影响。在6种CRC细胞系中表达水平各异。此外,敲低抑制了CRC细胞增殖和集落形成,导致细胞周期停滞并促进细胞凋亡。此外,敲低后,包括BAD和BAX在内的凋亡相关蛋白的表达水平升高,而Bcl-2表达降低。总之,本研究数据表明在结肠癌发生中起重要作用,但需要对这些数据背后的机制进行深入研究,以证明其是否可作为CRC治疗的新靶点。