Department of General Surgery, The First Affiliated Hospital of Anhui Medical University, Anhui, China.
Biomed Pharmacother. 2013 Sep;67(7):615-9. doi: 10.1016/j.biopha.2013.03.007. Epub 2013 Apr 3.
Because of increased insensitivity or resistance to chemical treatment in tumor patients, specific apoptotic gene silence may provide a rational approach for the development of novel therapeutic strategies. This study was to investigate whether downregulation of Bcl-2 expression by small interfering RNA (siRNA) against the Bcl-2 gene would enhance the apoptosis and sensitivity of gastric adenocarcinoma SGC-7901 cell to 5-Fluorouracil. Transfections of SGC-7901 cells with siRNA were performed using cationic liposomes. Sequence-specific downregulation of Bcl-2 expression was measured by RT-PCR and Western blot analysis. Cell proliferation assay was determined by MTT assay and apoptotic cell rates were determined by flow cytometry assay. Results showed that the siRNA could downregulate Bcl-2 expression, which increased apoptosis and sensitivity of SGC-7901 cell to 5-Fluorouracil (P<0.05). This study indicated that inhibition of Bcl-2 expression by siRNA would be useful a new useful protocol to increase the effect of 5-Fluorouracil on treatment of gastric adenocarcinoma, which may play an important role in developing novel therapeutic strategies in the future.
由于肿瘤患者对化学治疗的敏感性或耐药性增加,特定的凋亡基因沉默可能为开发新的治疗策略提供合理的方法。本研究旨在探讨针对 Bcl-2 基因的小干扰 RNA(siRNA)下调 Bcl-2 表达是否会增强胃癌腺癌细胞 SGC-7901 对 5-氟尿嘧啶的凋亡和敏感性。使用阳离子脂质体转染 SGC-7901 细胞。通过 RT-PCR 和 Western blot 分析测定 Bcl-2 表达的序列特异性下调。通过 MTT 测定法测定细胞增殖测定法,并通过流式细胞术测定凋亡细胞率。结果表明,siRNA 可以下调 Bcl-2 的表达,从而增加 SGC-7901 细胞对 5-氟尿嘧啶的凋亡和敏感性(P<0.05)。本研究表明,siRNA 抑制 Bcl-2 的表达可能是增加 5-氟尿嘧啶治疗胃癌效果的一种新的有用方案,这可能在未来的治疗策略开发中发挥重要作用。