The 476th Hospital of PLA, Fuzhou, Fujian 350025, China.
J Neurooncol. 2012 Mar;107(1):81-7. doi: 10.1007/s11060-011-0728-9. Epub 2011 Nov 16.
Livin, a novel member of the human inhibitors of apoptosis protein family, plays an important role in tumor progression and occurrence by inhibiting cell apoptosis. It is selectively expressed in the most common human neoplasms and appears to be involved in tumor cell resistance to chemotherapeutic agents. The present study was designed to investigate the potential of using RNA interference (RNAi) technique to downregulate Livin expression, and the subsequent effect on human glioma cells. The results showed that knockdown of Livin expression by short interfering RNA (siRNA) significantly inhibited glioma cell proliferation and increased cell apoptosis through cell arrest in the G(1)/G(0) phase of cell cycle in vitro. Furthermore, Livin siRNA significantly suppressed tumor growth in nude mice. Together, these findings suggest that RNAi-mediated downregulation of Livin expression could lead to potent antitumor activity in glioma cells and might serve as a novel therapeutic strategy in clinic.
生存素是人类凋亡抑制蛋白家族的新成员,通过抑制细胞凋亡在肿瘤的发生和发展中发挥重要作用。它在最常见的人类肿瘤中选择性表达,似乎与肿瘤细胞对化疗药物的耐药性有关。本研究旨在探讨利用 RNA 干扰(RNAi)技术下调生存素表达及其对人神经胶质瘤细胞的后续影响的可能性。结果表明,短发夹 RNA(siRNA)下调生存素表达可显著抑制神经胶质瘤细胞的增殖,并通过细胞周期 G1/G0 期阻滞诱导细胞凋亡。此外,生存素 siRNA 可显著抑制裸鼠肿瘤生长。综上所述,这些发现表明 RNAi 介导的生存素表达下调可导致神经胶质瘤细胞产生强大的抗肿瘤活性,并可能成为临床治疗的新策略。