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IP 受体生物学与内质网钙离子动力学在癌症中的作用

IP Receptor Biology and Endoplasmic Reticulum Calcium Dynamics in Cancer.

机构信息

Laboratory for Molecular and Cellular Signaling, Department of Cellular and Molecular Medicine & Leuven Cancer Institute, KU Leuven, Leuven, Belgium.

出版信息

Prog Mol Subcell Biol. 2021;59:215-237. doi: 10.1007/978-3-030-67696-4_11.

Abstract

Intracellular Ca signaling regulates a plethora of cellular functions. A central role in these processes is reserved for the inositol 1,4,5-trisphosphate receptor (IPR), a ubiquitously expressed Ca-release channel, mainly located in the endoplasmic reticulum (ER). Three IPR isoforms (IPR1, IPR2 and IPR3) exist, encoded respectively by ITPR1, ITPR2 and ITPR3. The proteins encoded by these genes are each about 2700 amino acids long and assemble into large tetrameric channels, which form the target of many regulatory proteins, including several tumor suppressors and oncogenes. Due to the important role of the IPRs in cell function, their dysregulation is linked to multiple pathologies. In this review, we highlight the complex role of the IPR in cancer, as it participates in most of the so-called "hallmarks of cancer". In particular, the IPR directly controls cell death and cell survival decisions via regulation of autophagy and apoptosis. Moreover, the IPR impacts cellular proliferation, migration and invasion. Typical examples of the role of the IPRs in these various processes are discussed. The relative levels of the IPR isoforms expressed and their subcellular localization, e.g. at the ER-mitochondrial interface, is hereby important. Finally, evidence is provided about how the knowledge of the regulation of the IPR by tumor suppressors and oncogenes can be exploited to develop novel therapeutic approaches to fight cancer.

摘要

细胞内钙信号调节着众多的细胞功能。在这些过程中,肌醇 1,4,5-三磷酸受体 (IPR) 起着核心作用,它是一种普遍表达的钙释放通道,主要位于内质网 (ER) 中。存在三种 IPR 同工型(IPR1、IPR2 和 IPR3),分别由 ITPR1、ITPR2 和 ITPR3 编码。这些基因编码的蛋白质每条都约 2700 个氨基酸长,并组装成大型四聚体通道,这些通道是许多调节蛋白的靶标,包括一些肿瘤抑制因子和癌基因。由于 IPR 在细胞功能中的重要作用,它们的失调与多种病理有关。在这篇综述中,我们强调了 IPR 在癌症中的复杂作用,因为它参与了大多数所谓的“癌症特征”。特别是,IPR 通过调节自噬和细胞凋亡直接控制细胞死亡和细胞存活的决定。此外,IPR 还影响细胞增殖、迁移和侵袭。讨论了 IPR 在这些不同过程中的典型作用。表达的 IPR 同工型的相对水平及其亚细胞定位,例如在内质网-线粒体界面,是很重要的。最后,提供了证据表明,如何利用肿瘤抑制因子和癌基因对 IPR 的调节知识来开发新的治疗癌症的方法。

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