Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, 200040, China.
Institute of Urology, Fudan University, Shanghai, 200040, China.
Appl Biochem Biotechnol. 2024 Apr;196(4):2233-2245. doi: 10.1007/s12010-023-04569-9. Epub 2023 Jul 26.
The mammalian target of rapamycin (mTOR) is a key regulatory molecular target to treat cancer, and MTI-31 is a potent mTOR inhibitory agent for the therapeutically target of the renal cell carcinoma (RCC). However, the therapeutic efficacy of MTI-31 is limited by multiple factors, including autophagy. MTI-31 can activate cells to generate autophagy, which may in turn indirectly affect cell proliferation and apoptosis. We aimed to observe changes in cell protective autophagy via the ERK pathway and explore the potential mechanism underlying drug resistance of RCC cells to MTI-31. Different concentrations of 786-O and RCC4 cells were co-cultured with MTI-31 for distinct durations. The result of autophagy marker detection by Western blot showed that MTI-31 could induce RCC cells to produce autophagy in a dose and time-dependent manner. After treating the RCC cells with the autophagy inhibitor chloroquine (CQ), CCK8 and Western blot assays demonstrated that CQ could effectively enhance cell apoptosis induced by MTI-31 and that the autophagy induced by MTI-31 was cytoprotective. In addition, CCK8 and Western blot demonstrated that MTI-31 exerted its effect by activating the ERK pathway rather than the JNK or p38 pathway. The use of the ERK inhibitor AZD6244 to block the ERK pathway could effectively promote cell apoptosis induced by MTI-31. AZD6244 attenuated the autophagy induced by MTI-31 and increased the cytotoxicity of MTI-31. Western blot also demonstrated that MTI-31-induced autophagy was mediated by the downstream regulators of ERK pathways, including Beclin-1 and Bcl-2. It demonstrated that the MTI-31 mediated activation ERK pathway is associated with the induction of autophagy, and autophagy can attenuate the cytotoxicity of MTI-31 on RCC cells. In summary, inhibition of ERK pathway-mediated autophagy can rectify drug resistance to MTI-31 effectively.
哺乳动物雷帕霉素靶蛋白(mTOR)是治疗癌症的关键调节分子靶标,MTI-31 是一种有效的 mTOR 抑制剂,用于治疗肾细胞癌(RCC)。然而,MTI-31 的治疗效果受到多种因素的限制,包括自噬。MTI-31 可以激活细胞产生自噬,这可能会间接影响细胞增殖和凋亡。我们旨在通过 ERK 通路观察细胞保护性自噬的变化,并探讨 RCC 细胞对 MTI-31 产生耐药性的潜在机制。将不同浓度的 786-O 和 RCC4 细胞与 MTI-31 共同培养不同时间。Western blot 检测自噬标志物的结果表明,MTI-31 可以剂量和时间依赖性地诱导 RCC 细胞产生自噬。用自噬抑制剂氯喹(CQ)处理 RCC 细胞后,CCK8 和 Western blot 实验表明,CQ 可以有效增强 MTI-31 诱导的细胞凋亡,并且 MTI-31 诱导的自噬具有细胞保护作用。此外,CCK8 和 Western blot 表明,MTI-31 通过激活 ERK 通路而不是 JNK 或 p38 通路发挥作用。使用 ERK 抑制剂 AZD6244 阻断 ERK 通路可以有效促进 MTI-31 诱导的细胞凋亡。AZD6244 减弱了 MTI-31 诱导的自噬,并增加了 MTI-31 的细胞毒性。Western blot 还表明,MTI-31 诱导的自噬是通过 ERK 通路的下游调节因子介导的,包括 Beclin-1 和 Bcl-2。这表明,MTI-31 介导的 ERK 通路的激活与自噬的诱导有关,自噬可以减轻 MTI-31 对 RCC 细胞的细胞毒性。综上所述,抑制 ERK 通路介导的自噬可以有效纠正 MTI-31 的耐药性。