Department of Molecular and Experimental Medicine, Avera Cancer Institute, Sioux Falls, SD ; Department of Internal Medicine, University of South Dakota, Vermillion, SD.
Department of Molecular and Experimental Medicine, Avera Cancer Institute, Sioux Falls, SD.
Neoplasia. 2014 Jan;16(1):43-72. doi: 10.1593/neo.131694.
Phosphoinositide 3-kinase (PI3K) pathway, in addition to its pro-proliferative and antiapoptotic effects on tumor cells, contributes to DNA damage repair (DDR). We hypothesized that GDC-0980, a dual PI3K-mammalian target of rapamycin (mTOR) inhibitor, would induce an efficient antitumor effect in BRCA-competent triple negative breast cancer (TNBC) model when combined with ABT888 and carboplatin. Mechanism-based in vitro studies demonstrated that GDC-0980 treatment alone or in combination led to DNA damage (increased pγH2AX(S139); Western blot, immunofluorescence), gain in poly ADP-ribose (PAR), and a subsequent sensitization of BRCA-competent TNBC cells to ABT888 plus carboplatin with a time-dependent 1) decrease in proliferation signals (pAKTT308/S473, pP70S6KT421/S424, pS6RPS235/236), PAR/poly(ADP-ribose) polymerase (PARP) ratios, PAR/pγH2AX ratios, live/dead cell ratios, cell cycle progression, and three-dimensional clonogenic growths and 2) increase in apoptosis markers (cleaved caspases 3 and 9, a pro-apoptotic BH3-only of Bcl-2 family (BIM), cleaved PARP, annexin V). The combination was effective in vitro in BRCA-wild-type PIK3CA-H1047R-mutated BT20 and PTEN-null HCC70 cells. The combination blocked the growth of established xenograft tumors by 80% to 90% with a concomitant decrease in tumor Ki67, CD31, phosphorylated vascular endothelial growth factor receptor, pS6RPS235/236, and p4EBP1T37/46 as well as an increase in cleaved caspase 3 immunohistochemistry (IHC) levels. Interestingly, a combination with GDC-0941, a pan-PI3K inhibitor, failed to block the tumor growth in MDA-MB231. Results demonstrate that the dual inhibition of PI3K and mTOR regulates DDR. In a BRCA-competent model, GDC-0980 enhanced the antitumor activity of ABT888 plus carboplatin by inhibiting both tumor cell proliferation and tumor-induced angiogenesis along with an increase in the tumor cell apoptosis. This is the first mechanism-based study to demonstrate the integral role of the PI3K-AKT-mTOR pathway in DDR-mediated antitumor action of PARP inhibitor in TNBC.
磷酸肌醇 3-激酶 (PI3K) 途径除了对肿瘤细胞具有促增殖和抗凋亡作用外,还参与 DNA 损伤修复 (DDR)。我们假设,双重 PI3K-哺乳动物雷帕霉素靶蛋白 (mTOR) 抑制剂 GDC-0980 与 ABT888 和卡铂联合使用时,在 BRCA 功能正常的三阴性乳腺癌 (TNBC) 模型中会产生有效的抗肿瘤作用。基于机制的体外研究表明,GDC-0980 单独或联合治疗导致 DNA 损伤 (增加 pγH2AX(S139);Western blot、免疫荧光)、聚 ADP-核糖 (PAR) 增加,以及随后 BRCA 功能正常的 TNBC 细胞对 ABT888 加卡铂的敏感性增加,具有时间依赖性 1)减少增殖信号 (pAKTT308/S473、pP70S6KT421/S424、pS6RPS235/236)、PAR/PARP 比、PAR/pγH2AX 比、活/死细胞比、细胞周期进程和三维克隆生长,以及 2)增加凋亡标志物 (cleaved caspases 3 和 9、Bcl-2 家族的促凋亡 BH3-only (BIM)、cleaved PARP、annexin V)。该组合在 BRCA 野生型 PIK3CA-H1047R 突变 BT20 和 PTEN 缺失 HCC70 细胞中在体外具有疗效。该组合通过 80%至 90%的比例阻断已建立的异种移植肿瘤的生长,同时降低肿瘤 Ki67、CD31、磷酸化血管内皮生长因子受体、pS6RPS235/236 和 p4EBP1T37/46 的水平,并增加 cleaved caspase 3 免疫组化 (IHC) 水平。有趣的是,与 GDC-0941(一种泛 PI3K 抑制剂)联合使用未能阻止 MDA-MB231 中的肿瘤生长。结果表明,PI3K 和 mTOR 的双重抑制通过抑制肿瘤细胞增殖和肿瘤诱导的血管生成以及增加肿瘤细胞凋亡来调节 DDR。在 BRCA 功能正常的模型中,GDC-0980 通过抑制肿瘤细胞增殖和肿瘤诱导的血管生成以及增加肿瘤细胞凋亡,增强了 ABT888 加卡铂的抗肿瘤活性。这是第一项基于机制的研究,证明了 PI3K-AKT-mTOR 通路在 PARP 抑制剂介导的 TNBC 肿瘤 DDR 抗肿瘤作用中的整体作用。