Visa Anna, Alza Lía, Casas-Benito Adrian, Herreros Judit, Cantí Carles
Universitat de Lleida-IRBlleida, Lleida, Spain.
Universitat de Lleida-IRBlleida, Lleida, Spain.
Drug Discov Today. 2022 Mar;27(3):743-758. doi: 10.1016/j.drudis.2021.11.021. Epub 2021 Nov 24.
Over the past 20 years, various studies have demonstrated a pivotal role of T-type calcium channels (TTCCs) in tumor progression. Cytotoxic effects of TTCC pharmacological blockers have been reported in vitro and in preclinical models. However, their roles in cancer physiology are only beginning to be understood. In this review, we discuss evidence for the signaling pathways and cellular processes stemming from TTCC activity, mainly inferred by inverse reasoning from pharmacological blocks and, only in a few studies, by gene silencing or channel activation. A thorough analysis indicates that drug-induced cytotoxicity is partially an off-target effect. Dissection of on/off-target activity is paramount to elucidate the physiological roles of TTCCs, and to deliver efficacious therapies suited to different cancer types and stages.
在过去20年里,多项研究表明T型钙通道(TTCCs)在肿瘤进展中起关键作用。TTCC药理学阻滞剂的细胞毒性作用已在体外和临床前模型中得到报道。然而,它们在癌症生理学中的作用才刚刚开始被了解。在这篇综述中,我们讨论了源于TTCC活性的信号通路和细胞过程的证据,这些证据主要通过药理学阻断的反向推理得出,仅在少数研究中通过基因沉默或通道激活得出。深入分析表明,药物诱导的细胞毒性部分是脱靶效应。剖析靶标活性对于阐明TTCCs的生理作用以及提供适合不同癌症类型和阶段的有效治疗至关重要。