Potential functions of TRPM2 and TRPM7 channels in the tumor microenvironment.

IF 3.6 3区 医学 Q3 CELL BIOLOGY
Irma Yadira Izaguirre-Hernández, Adriana Sumoza-Toledo
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引用次数: 0

Abstract

The tumor microenvironment (TME) is a complex and dynamic ecosystem consisting of both cellular and non-cellular components that collectively modulate the anti-tumor immune response, as well as cancer growth, invasion, metastasis, immune evasion, and resistance to therapy. Calcium (Ca2+) and magnesium (Mg2+) are two essential ions for a wide range of cellular processes including proliferation, differentiation, migration and protein secretion. The intracellular homeostasis and spatio-temporal distribution of these two ions are tightly regulated by ion channels, notably members of the transient receptor potential melastatin (TRPM) subfamily such as TRPM2 and TRPM7. TRPM2 is a Ca2+-permeable channel activated by ADP-ribose (ADPR) and reactive oxygen species (ROS), whereas TRPM7 permeates both Ca2+ and Mg2+ ions and exhibit constitutive activity. Both channels have been involved in redox-sensitive signaling and function as temperature sensors across various physiological and pathological context, such as cancer. Here we provide an overview of the potential roles of TRPM2 and TRPM7 in regulating cellular dynamics within the TME, with a focus on their contributions to immune modulation.

TRPM2和TRPM7通道在肿瘤微环境中的潜在功能。
肿瘤微环境(TME)是一个复杂的、动态的生态系统,由细胞和非细胞成分组成,它们共同调节抗肿瘤免疫反应,以及肿瘤的生长、侵袭、转移、免疫逃避和对治疗的抵抗。钙(Ca2+)和镁(Mg2+)是细胞增殖、分化、迁移和蛋白质分泌等一系列细胞过程中必不可少的两个离子。这两种离子的细胞内稳态和时空分布受到离子通道的严格调控,尤其是瞬时受体电位美拉抑素(TRPM)亚家族成员,如TRPM2和TRPM7。TRPM2是一种由adp核糖(ADPR)和活性氧(ROS)激活的Ca2+渗透通道,而TRPM7同时渗透Ca2+和Mg2+离子并表现出组成活性。这两个通道都参与氧化还原敏感信号传导,并在各种生理和病理环境(如癌症)中作为温度传感器发挥作用。在这里,我们概述了TRPM2和TRPM7在调节TME内细胞动力学中的潜在作用,重点介绍了它们对免疫调节的贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Leukocyte Biology
Journal of Leukocyte Biology 医学-免疫学
CiteScore
11.50
自引率
0.00%
发文量
358
审稿时长
2 months
期刊介绍: JLB is a peer-reviewed, academic journal published by the Society for Leukocyte Biology for its members and the community of immunobiologists. The journal publishes papers devoted to the exploration of the cellular and molecular biology of granulocytes, mononuclear phagocytes, lymphocytes, NK cells, and other cells involved in host physiology and defense/resistance against disease. Since all cells in the body can directly or indirectly contribute to the maintenance of the integrity of the organism and restoration of homeostasis through repair, JLB also considers articles involving epithelial, endothelial, fibroblastic, neural, and other somatic cell types participating in host defense. Studies covering pathophysiology, cell development, differentiation and trafficking; fundamental, translational and clinical immunology, inflammation, extracellular mediators and effector molecules; receptors, signal transduction and genes are considered relevant. Research articles and reviews that provide a novel understanding in any of these fields are given priority as well as technical advances related to leukocyte research methods.
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