Shi Qian, Yang Zijing, Yang Huan, Xu Lihui, Xia Jing, Gu Jie, Chen Mengting, Wang Yan, Zhao Xiaohong, Liao Zehua, Mou Yiping, Gu Xidong, Xie Tian, Sui Xinbing
School of Pharmacy, Hangzhou Normal University, Hangzhou, Zhejiang, China.
General Surgery, Cancer Center, Department of Gastrointestinal-Pancreatic Surgery, Zhejiang Provincial People's Hospital, Hangzhou Medical University, Hangzhou, Zhejiang, China.
Theranostics. 2025 Jan 1;15(2):521-545. doi: 10.7150/thno.103384. eCollection 2025.
Ion channels, as functional molecules that regulate the flow of ions across cell membranes, have emerged as a promising target in cancer therapy due to their pivotal roles in cell proliferation, metastasis, apoptosis, drug resistance, and so on. Recently, increasing evidence suggests that dysregulation of ion channels is a common characteristic of cancer cells, contributing to their survival and the resistance to conventional therapies. For example, the aberrant expression of sodium (Na) and potassium ion (K) channels is significantly correlated with the sensitivity of chemotherapy drugs. The endogenous calcium (Ca) channels contribute to the acquired resistance of osimertinib in epidermal growth factor receptor (EGFR) mutant non-small cell lung cancer cell lines. Ferrous ions (Fe) enhance the sensitivity of breast cancer cells to doxorubicin treatment. Preclinical models have also demonstrated the effect of specific ion channel blockers or modulators on anticancer drug resistance. This review describes the current understanding about the interaction between ion channels and the therapeutic efficacy of anticancer drugs. Then, the therapeutic potential of ion channel blockers or modulators in enhancing the sensitivity or overcoming the resistance of cancer cells to anticancer therapies is discussed. Targeting ion channels will hopefully offer a novel and promising strategy for overcoming cancer drug resistance.
离子通道作为调节离子跨细胞膜流动的功能分子,由于其在细胞增殖、转移、凋亡、耐药性等方面的关键作用,已成为癌症治疗中一个有前景的靶点。最近,越来越多的证据表明,离子通道失调是癌细胞的一个共同特征,有助于其生存和对传统疗法的耐药性。例如,钠(Na)和钾离子(K)通道的异常表达与化疗药物的敏感性显著相关。内源性钙(Ca)通道导致表皮生长因子受体(EGFR)突变的非小细胞肺癌细胞系对奥希替尼产生获得性耐药。亚铁离子(Fe)增强乳腺癌细胞对多柔比星治疗的敏感性。临床前模型也证明了特定离子通道阻滞剂或调节剂对抗癌药物耐药性的影响。本综述描述了目前对离子通道与抗癌药物治疗效果之间相互作用的理解。然后,讨论了离子通道阻滞剂或调节剂在提高癌细胞对抗癌治疗的敏感性或克服耐药性方面的治疗潜力。靶向离子通道有望为克服癌症耐药性提供一种新的、有前景的策略。