Yeoh Yeelon, Low Teck Yew, Abu Nadiah, Lee Pey Yee
UKM Medical Molecular Biology Institute (UMBI), Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
PeerJ. 2021 Oct 22;9:e12338. doi: 10.7717/peerj.12338. eCollection 2021.
Resistance to anti-cancer treatments is a critical and widespread health issue that has brought serious impacts on lives, the economy and public policies. Mounting research has suggested that a selected spectrum of patients with advanced colorectal cancer (CRC) tend to respond poorly to both chemotherapeutic and targeted therapeutic regimens. Drug resistance in tumours can occur in an intrinsic or acquired manner, rendering cancer cells insensitive to the treatment of anti-cancer therapies. Multiple factors have been associated with drug resistance. The most well-established factors are the emergence of cancer stem cell-like properties and overexpression of ABC transporters that mediate drug efflux. Besides, there is emerging evidence that signalling pathways that modulate cell survival and drug metabolism play major roles in the maintenance of multidrug resistance in CRC. This article reviews drug resistance in CRC as a result of alterations in the MAPK, PI3K/PKB, Wnt/β-catenin and Notch pathways.
抗癌治疗耐药性是一个关键且普遍存在的健康问题,已对生命、经济和公共政策造成严重影响。越来越多的研究表明,一部分晚期结直肠癌(CRC)患者往往对化疗和靶向治疗方案反应不佳。肿瘤中的耐药性可通过内在或获得性方式产生,使癌细胞对抗癌治疗不敏感。多种因素与耐药性相关。最明确的因素是癌症干细胞样特性的出现以及介导药物外排的ABC转运蛋白的过表达。此外,越来越多的证据表明,调节细胞存活和药物代谢的信号通路在CRC多药耐药性的维持中起主要作用。本文综述了由于MAPK、PI3K/PKB、Wnt/β-连环蛋白和Notch信号通路改变导致的CRC耐药性。