Division of Respiratory Medicine, Medizinische Klinik-Innenstadt, Ziemssenstr. 1, 80336 Munich, Germany.
Anticancer Res. 2011 Mar;31(3):849-54.
BEZ235 is a dual phosphatidylinositol 3-kinase (PI(3)K)/mammalian target of rapamycin (mTOR) inhibitor that is orally available and that has been shown to be effective in several malignancies in vitro. Recently, BEZ235 entered clinical trials for solid tumors. We aimed at investigating if BEZ235 is effective in lung cancer cell lines.
The human lung cancer cell lines EPLC, HCC and H1339 were analysed by fluorescence in situ hybridization, gene sequencing and Western blot analysis. Cells were exposed to BEZ235 and/or cisplatin and the survival fraction was quantified.
In all cell lines, BEZ235 reduced pAkt and pS6 expression indicating interference with the epidermal growth factor (EGF) pathway. Furthermore, BEZ235 inhibited tumor cell growth and added to the effects of cisplatin. This was independent of EGFR amplification and EGFR, KRAS, PI3K and AKT mutation.
The dual PI3K/mTOR inhibitor BEZ235 is effective in lung cancer cell lines and a promising compound to be tested in clinical phase I studies.
BEZ235 是一种口服的双重磷脂酰肌醇 3-激酶(PI(3)K)/哺乳动物雷帕霉素靶蛋白(mTOR)抑制剂,已在体外多种恶性肿瘤中显示出疗效。最近,BEZ235 已进入实体瘤的临床试验阶段。我们旨在研究 BEZ235 是否对肺癌细胞系有效。
通过荧光原位杂交、基因测序和 Western blot 分析对人肺癌细胞系 EPLC、HCC 和 H1339 进行分析。将细胞暴露于 BEZ235 和/或顺铂,并定量存活分数。
在所有细胞系中,BEZ235 降低了 pAkt 和 pS6 的表达,表明其干扰了表皮生长因子(EGF)通路。此外,BEZ235 抑制肿瘤细胞生长,并增强了顺铂的作用。这与 EGFR 扩增以及 EGFR、KRAS、PI3K 和 AKT 突变无关。
双重 PI3K/mTOR 抑制剂 BEZ235 对肺癌细胞系有效,是一种很有前途的化合物,值得在临床 I 期研究中进行测试。