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TRPM 在黑素细胞和黑色素瘤中的作用。

Role of TRPM in melanocytes and melanoma.

机构信息

Department of Pathology, Westchester Medical Center, New York Medical College, Valhalla, NY, USA.

出版信息

Exp Dermatol. 2012 Sep;21(9):650-4. doi: 10.1111/j.1600-0625.2012.01565.x.

DOI:10.1111/j.1600-0625.2012.01565.x
PMID:22897572
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3422761/
Abstract

Transient receptor potential (TRP) cation channel superfamily plays important roles in variety cellular processes including polymodal cellular sensing, cell adhesion, cell polarity, proliferation, differentiation and apoptosis. One of its subfamilies are TRPM channels. mRNA expression of its founding member, TRPM1 (melastatin), correlates with terminal melanocytic differentiation and loss of its expression has been identified as an important diagnostic and prognostic marker for primary cutaneous melanoma. Because TRPM1 gene codes two transcripts: TRPM1 channel protein in its exons and miR-211 in one of its introns, we propose a dual role for TRPM1 gene where the loss of TRPM1 channel protein is an excellent marker of melanoma aggressiveness, while the expression of miR-211 is linked to the tumor suppressor function of TRPM1. In addition, three other members of this subfamily, TRPM 2, 7 and 8 are implicated in the regulation of melanocytic behaviour. TRPM2 is capable of inducing melanoma apoptosis and necrosis. TRPM7 can be a protector and detoxifier in both melanocytes and melanoma cells. TRPM8 can mediate agonist-induced melanoma cell death. Therefore, we propose that TRPM1, TRPM2, TRPM7 and TRPM8 play crucial roles in melanocyte physiology and melanoma oncology and are excellent diagnostic markers and theraputic targets.

摘要

瞬时受体电位 (TRP) 阳离子通道超家族在多种细胞过程中发挥重要作用,包括多模态细胞感应、细胞黏附、细胞极性、增殖、分化和凋亡。其亚家族之一是 TRPM 通道。其创始成员 TRPM1(melastatin)的 mRNA 表达与终末黑素细胞分化相关,其表达的丧失已被确定为原发性皮肤黑素瘤的重要诊断和预后标志物。因为 TRPM1 基因编码两个转录本:其外显子中的 TRPM1 通道蛋白和其一个内含子中的 miR-211,我们提出 TRPM1 基因具有双重作用,TRPM1 通道蛋白的丧失是黑色素瘤侵袭性的极好标志物,而 miR-211 的表达与 TRPM1 的肿瘤抑制功能相关。此外,该亚家族的另外三个成员,TRPM2、7 和 8,参与了黑素细胞行为的调节。TRPM2 能够诱导黑色素瘤细胞凋亡和坏死。TRPM7 可以在黑素细胞和黑色素瘤细胞中充当保护剂和解毒剂。TRPM8 可以介导激动剂诱导的黑色素瘤细胞死亡。因此,我们提出 TRPM1、TRPM2、TRPM7 和 TRPM8 在黑素细胞生理学和黑色素瘤肿瘤学中发挥着至关重要的作用,是极好的诊断标志物和治疗靶点。

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Recent trends in cutaneous melanoma incidence and death rates in the United States, 1992-2006.美国 1992-2006 年皮肤黑色素瘤发病率和死亡率的最新趋势。
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Transient receptor potential channels as therapeutic targets.瞬时受体电位通道作为治疗靶点。
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The odyssey of the TR(i)P journey to the cellular membrane.TR(i)P向细胞膜的旅程奇遇。
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PLoS One. 2010 Nov 1;5(11):e13779. doi: 10.1371/journal.pone.0013779.