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The down-regulation of SNCG inhibits the proliferation and invasiveness of human bladder cancer cell line 5637 and suppresses the expression of MMP-2/9

机译:SNCG的下调抑制了人膀胱癌细胞系5637的增殖和侵袭性抑制了MMP-2/9的表达

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摘要

γ-synuclein (SNCG) is highly expressed in bladder cancer tissues and associated with tumor recurrence. However, the functional effect of SNCG on the development of bladder cancer remains unknown. In the present study, the effects of SNCG down-regulation by RNA interference (RNAi) on the proliferation and invasiveness of human bladder cancer cell line 5637 were explored. Three pairs of SNCG-specific small interference RNA (siRNA) were designed and transfected into the 5637 cell lines, and then the SNCG expressions in the three siRNA were assessed using reverse transcription-polymerase chain reactions (RT-PCR) and Western blot, while the cell proliferation and invasiveness of the 5637 cells were evaluated using cell counting kit-8 (CCK-8) and transwell assays, respectively. In addition, the expressions of matrix metalloproteinase-2 and -9 (MMP-2/9) were analyzed using enzyme-linked immunosorbent assays after the down-regulation of SNCG. The results showed that compared with the negative and empty vector controls, all three SNCG siRNAs were observed to significantly inhibit the SNCG expressions at the mRNA and protein levels (P < 0.05), among which the lowest SNCG expression was measured in SNCG-siRNA-244. And the SNCG suppression mediated by RNAi successfully inhibited the proliferation and invasiveness of the 5637 cell lines (P < 0.05), as well as the down-regulation of MMP-2/9. In conclusion, the proliferation and invasiveness of bladder cancer cells can be decreased by specifically interfering with the SNCG expression. And SNCG siRNA deserves further study as a novel target for biomedical therapy in bladder cancer.
机译:γ-突触核蛋白(SNCG)在膀胱癌组织中高度表达并与肿瘤复发相关。然而,SNCG对膀胱癌发展的功能作用仍然未知。在本研究中,探讨了RNA干扰(RNAi)对人膀胱癌细胞系5637的增殖和侵袭性的影响。设计并转染三对SNCG特异性小干扰RNA(siRNA),然后使用逆转录 - 聚合酶链反应(RT-PCR)和Western印迹评估三个siRNA中的SNCG表达。使用细胞计数试剂盒-8(CCK-8)和Transwell测定来评估5637细胞的细胞增殖和侵袭。此外,使用在SNCG的下调后使用酶联免疫吸附测定分析基质金属蛋白酶-2和-9(MMP-2/9)的表达。结果表明,与阴性和空载体对照相比,所有三个SNCG siRNA被观察到显着抑制mRNA和蛋白质水平的SNCG表达(P <0.05),其中在SNCG-siRNA中测量最低的SNCG表达式 - 244。通过RNAi介导的SNCG抑制成功抑制了5637细胞系(P <0.05)的增殖和侵袭性,以及MMP-2/9的下调。总之,通过特异性干扰SNCG表达可以降低膀胱癌细胞的增殖和侵袭。 SNCG siRNA值得进一步研究作为膀胱癌的生物医学治疗的新靶点。

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