Ca2+ 稳态:癌症疗法的潜在靶点。

Min Su, Shanliang Zheng, Hao Liu, Tie-Shan Tang, Ying Hu
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引用次数: 0

摘要

钙离子(Ca2+)作为次级信使,在可兴奋和不可兴奋细胞中都发挥着至关重要的作用。参与钙处理的蛋白质和分子系统十分复杂,可传递 Ca2+ 信号。在癌细胞中,这些钙处理工具包蛋白的突变、异常表达和失调会破坏细胞外空间、细胞膜、内质网和线粒体之间正常的 Ca2+ 通量,以及 Ca2+ 信号的时空模式。这导致钙依赖效应器失调,而钙依赖效应器控制着癌细胞增殖、存活和侵袭的关键信号通路。尽管在了解癌细胞中钙平衡的重塑和确定促进恶性表型的关键钙转运分子方面取得了进展,但要将这些基本发现转化为通过靶向 Ca2+ 平衡诊断和治疗癌症的新工具,仍有许多工作要做。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ca2+ homeostasis: a potential target for cancer therapies.

Calcium ions (Ca2+) play a crucial role as secondary messengers in both excitable and non-excitable cells. A complex system of proteins and molecules involved in calcium handling allows Ca2+ signals to be transduced. In cancer cells, mutations, aberrant expression, and dysregulation of these calcium handling toolkit proteins disrupt the normal Ca2+ flux between extracellular space, cytosol, endoplasmic reticulum and mitochondria, as well as the spatio-temporal patterns of Ca2+ signalling. This leads to the dysregulation of calcium-dependent effectors that control key signaling pathways involved in cancer cell proliferation, survival and invasion. Although there has been progressing in understanding the remodelling of calcium homeostasis in cancer cells and identifying key calcium transport molecules that promote malignant phenotypes, much work remains to be done to translate these fundamental findings into new tools for diagnosing and treating cancer by targeting Ca2+ homeostasis.

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