Department of Pharmaceutical Sciences and Natural Products, Central University of Punjab, Ghudda, Bathinda, 151401, India.
Med Oncol. 2022 Oct 29;40(1):3. doi: 10.1007/s12032-022-01864-z.
Thymidylate synthase is the rate-limiting enzyme required for DNA synthesis and overexpression of this enzyme causes resistance to cancer cells. Long treatments with 5-FU cause resistance to Thymidylate synthase targeting drugs. We have also compiled different mechanisms of drug resistance including autophagy and apoptosis, drug detoxification and ABC transporters, drug efflux, signaling pathways (AKT/PI3K, RAS-MAPK, WNT/β catenin, mTOR, NFKB, and Notch1 and FOXM1) and different genes associated with resistance in colorectal cancer. We can overcome 5-FU resistance in cancer cells by regulating thymidylate synthase by natural products (Coptidis rhizoma), HDAC inhibitors, mTOR inhibitors, Folate antagonists, and several other drugs which have been used in combination with TS inhibitors. This review is a compilation of different approaches reported for the regulation of thymidylate synthase to overcome resistance in colorectal cancer cells.
胸苷酸合成酶是 DNA 合成所需的限速酶,这种酶的过度表达导致癌细胞产生耐药性。5-FU 的长期治疗会导致胸苷酸合成酶靶向药物产生耐药性。我们还总结了不同的耐药机制,包括自噬和细胞凋亡、药物解毒和 ABC 转运体、药物外排、信号通路(AKT/PI3K、RAS-MAPK、WNT/β-catenin、mTOR、NFKB 和 Notch1 和 FOXM1)以及与结直肠癌耐药相关的不同基因。我们可以通过天然产物(黄连)、组蛋白去乙酰化酶抑制剂、mTOR 抑制剂、叶酸拮抗剂和其他几种已与 TS 抑制剂联合使用的药物来调节胸苷酸合成酶,从而克服癌细胞对 5-FU 的耐药性。这篇综述是对为克服结直肠癌细胞耐药性而调节胸苷酸合成酶的不同方法的总结。