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GPCRs CysLTR1/2 介导的信号通路在黑素细胞增殖和衰老中的作用。

The role of signaling pathways mediated by the GPCRs CysLTR1/2 in melanocyte proliferation and senescence.

机构信息

Laboratory of Chemical Biology and Signal Transduction, Rockefeller University, New York, NY 10065, USA.

Tri-Institutional PhD Program in Chemical Biology, New York, NY 10065, USA.

出版信息

Sci Signal. 2024 Sep 17;17(854):eadp3967. doi: 10.1126/scisignal.adp3967.

DOI:10.1126/scisignal.adp3967
PMID:39288219
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11920964/
Abstract

In contrast with sun exposure-induced melanoma, rarer melanocytic tumors and neoplasms with low mutational burden present opportunities to study isolated signaling mechanisms. These include uveal melanoma and blue nevi, which are often driven by mutations within the G protein-coupled signaling cascade downstream of cysteinyl leukotriene receptor 2. Here, we review how the same mutations within this pathway drive the growth of melanocytes in one tissue but can inhibit the growth of those in another, exemplifying the role of the tissue environment in the delicate balance between uncontrolled cell growth and senescence.

摘要

与阳光照射引起的黑色素瘤相反,罕见的黑色素细胞肿瘤和突变负担较低的肿瘤为研究孤立的信号机制提供了机会。这些肿瘤包括葡萄膜黑色素瘤和蓝色痣,它们通常由半胱氨酰白三烯受体 2 下游的 G 蛋白偶联信号级联中的突变驱动。在这里,我们回顾了该途径中的相同突变如何驱动一种组织中黑素细胞的生长,但又可以抑制另一种组织中黑素细胞的生长,这说明了组织环境在失控的细胞生长和衰老之间的微妙平衡中的作用。

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Formyl Peptide Receptor 2-Dependent cPLA2 and 5-LOX Activation Requires a Functional NADPH Oxidase.甲酰肽受体2依赖性的胞浆型磷脂酶A2和5-脂氧合酶激活需要功能性NADPH氧化酶。
Antioxidants (Basel). 2024 Feb 8;13(2):220. doi: 10.3390/antiox13020220.
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1,4-dihydroxy quininib activates ferroptosis pathways in metastatic uveal melanoma and reveals a novel prognostic biomarker signature.
1,4-二羟基奎尼inib激活转移性葡萄膜黑色素瘤中的铁死亡途径,并揭示一种新的预后生物标志物特征。
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INPP5A phosphatase is a synthetic lethal target in GNAQ and GNA11-mutant melanomas.INPP5A 磷酸酶是 GNAQ 和 GNA11 突变型黑色素瘤的合成致死靶点。
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High-throughput chemogenetic drug screening reveals PKC-RhoA/PKN as a targetable signaling vulnerability in GNAQ-driven uveal melanoma.高通量化学遗传学药物筛选揭示 PKC-RhoA/ PKN 是 GNAQ 驱动的葡萄膜黑素瘤中可靶向的信号脆弱性靶点。
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