Institute of Toxicology, University Medical Center Mainz, Obere Zahlbacher Str. 67, D-55131 Mainz, Germany.
Cells. 2022 Aug 19;11(16):2588. doi: 10.3390/cells11162588.
A first-line therapeutic for high-grade glioma, notably glioblastoma (GBM), is the DNA methylating drug temozolomide (TMZ). Previously, we showed that TMZ induces not only apoptosis and autophagy, but also cellular senescence (CSEN). We presented the hypothesis that GBM cells may escape from CSEN, giving rise to recurrent tumors. Furthermore, the inflammatory phenotype associated with CSEN may attenuate chemotherapy and drive tumor progression. Therefore, treatments that specifically target senescent cells, i.e., senolytic drugs, may lead to a better outcome of GBM therapy by preventing recurrences and tumor inflammation. Here, we tested Bcl-2 targeting drugs including ABT-737, ABT-263 (navitoclax), several natural substances such as artesunate, fisetin and curcumin as well as lomustine (CCNU) and ionizing radiation (IR) for their senolytic capacity in GBM cells. Additionally, several proteins involved in the DNA damage response (DDR), ATM, ATR, Chk1/2, p53, p21, NF-kB, Rad51, PARP, IAPs and autophagy, a pathway involved in CSEN induction, were tested for their impact in maintaining CSEN. Treatment of GBM cells with a low dose of TMZ for 8-10 days resulted in >80% CSEN, confirming CSEN to be the major trait induced by TMZ. To identify senolytics, we treated the senescent population with the compounds of interest and found that ABT-737, navitoclax, chloroquine, ATMi, ATRi, BV-6, PX-866 and the natural compounds fisetin and artesunate exhibit senolytic activity, inducing death in senescent cells more efficiently than in proliferating cells. Curcumin showed the opposite effect. No specific effect on CSEN cells was observed by inhibition of Chk1/Chk2, p21, NF-kB, Rad51 and PARP. We conclude that these factors neither play a critical role in maintaining TMZ-induced CSEN nor can their inhibitors be considered as senolytics. Since IR and CCNU did not exhibit senolytic activity, radio- and chemotherapy with alkylating drugs is not designed to eliminate TMZ-induced senescent cancer cells.
替莫唑胺(TMZ)是高级别神经胶质瘤(尤其是胶质母细胞瘤,GBM)的一线治疗药物。此前,我们发现 TMZ 不仅能诱导细胞凋亡和自噬,还能诱导细胞衰老(CSEN)。我们提出假设,即 GBM 细胞可能会逃避 CSEN,从而产生复发性肿瘤。此外,与 CSEN 相关的炎症表型可能会减弱化疗效果并促进肿瘤进展。因此,专门针对衰老细胞的治疗方法(即衰老细胞清除药物),通过防止复发和肿瘤炎症,可能会改善 GBM 治疗的效果。在这里,我们测试了包括 ABT-737、ABT-263(navitoclax)在内的 Bcl-2 靶向药物、青蒿琥酯、非瑟酮和姜黄素等几种天然物质以及洛莫司汀(CCNU)和电离辐射(IR),以确定它们在 GBM 细胞中的衰老细胞清除能力。此外,还测试了参与 DNA 损伤反应(DDR)的几种蛋白(ATM、ATR、Chk1/Chk2、p53、p21、NF-kB、Rad51、PARP、IAPs 和自噬,这是 CSEN 诱导所涉及的途径),以确定它们在维持 CSEN 中的作用。用低剂量 TMZ 处理 GBM 细胞 8-10 天可导致>80%的 CSEN,证实 CSEN 是 TMZ 诱导的主要特征。为了鉴定衰老细胞清除剂,我们用感兴趣的化合物处理衰老细胞群,发现 ABT-737、navitoclax、氯喹、ATR 抑制剂、BV-6、PX-866 以及天然化合物非瑟酮和青蒿琥酯具有衰老细胞清除活性,在衰老细胞中的诱导死亡比在增殖细胞中更有效。姜黄素则表现出相反的效果。抑制 Chk1/Chk2、p21、NF-kB、Rad51 和 PARP 对 CSEN 细胞没有特定作用。我们得出的结论是,这些因素既不是维持 TMZ 诱导的 CSEN 的关键因素,也不能将其抑制剂视为衰老细胞清除剂。由于 IR 和 CCNU 没有表现出衰老细胞清除活性,因此用烷化剂进行放射和化学疗法不是为了消除 TMZ 诱导的衰老癌细胞。