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内质网-线粒体钙转运的调控及其在抗癌治疗中的重要性

Regulation of Endoplasmic Reticulum-Mitochondria Ca Transfer and Its Importance for Anti-Cancer Therapies.

作者信息

Pedriali Gaia, Rimessi Alessandro, Sbano Luigi, Giorgi Carlotta, Wieckowski Mariusz R, Previati Maurizio, Pinton Paolo

机构信息

Department of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, Laboratory for Technologies of Advanced Therapies (LTTA), University of Ferrara, Ferrara, Italy.

Department of Biochemistry, Nencki Institute of Experimental Biology, Warsaw, Poland.

出版信息

Front Oncol. 2017 Aug 31;7:180. doi: 10.3389/fonc.2017.00180. eCollection 2017.

Abstract

Inter-organelle membrane contact sites are emerging as major sites for the regulation of intracellular Ca concentration and distribution. Here, extracellular stimuli operate on a wide array of channels, pumps, and ion exchangers to redistribute intracellular Ca among several compartments. The resulting highly defined spatial and temporal patterns of Ca movement can be used to elicit specific cellular responses, including cell proliferation, migration, or death. Plasma membrane (PM) also can directly contact mitochondria and endoplasmic reticulum (ER) through caveolae, small invaginations of the PM that ensure inter-organelle contacts, and can contribute to the regulation of numerous cellular functions through scaffolding proteins such as caveolins. PM and ER organize specialized junctions. Here, many components of the receptor-dependent Ca signals are clustered, including the ORAI1-stromal interaction molecule 1 complex. This complex constitutes a primary mechanism for Ca entry into non-excitable cells, modulated by intracellular Ca. Several contact sites between the ER and mitochondria, termed mitochondria-associated membranes, show a very complex and specialized structure and host a wide number of proteins that regulate Ca transfer. In this review, we summarize current knowledge of the particular action of several oncogenes and tumor suppressors at these specialized check points and analyze anti-cancer therapies that specifically target Ca flow at the inter-organelle contacts to alter the metabolism and fate of the cancer cell.

摘要

细胞器间膜接触位点正逐渐成为调节细胞内钙浓度和分布的主要场所。在此,细胞外刺激作用于多种通道、泵和离子交换器,以在多个区室之间重新分配细胞内钙。由此产生的高度明确的钙移动时空模式可用于引发特定的细胞反应,包括细胞增殖、迁移或死亡。质膜(PM)也可通过小窝直接与线粒体和内质网(ER)接触,小窝是质膜的小内陷,可确保细胞器间的接触,并可通过诸如小窝蛋白等支架蛋白参与多种细胞功能的调节。质膜和内质网形成特化连接。在此,受体依赖性钙信号的许多成分聚集在一起,包括ORAI1-基质相互作用分子1复合物。该复合物构成了钙进入非兴奋性细胞的主要机制,受细胞内钙的调节。内质网和线粒体之间的几个接触位点,称为线粒体相关膜,具有非常复杂和特化的结构,并容纳大量调节钙转运的蛋白质。在本综述中,我们总结了目前关于几种癌基因和肿瘤抑制因子在这些特化检查点的特定作用的知识,并分析了专门针对细胞器间接触处钙流以改变癌细胞代谢和命运的抗癌疗法。

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