ASIC3 激活的新脂质合成关键酶支持乳酸驱动的 EMT 和结直肠癌细胞的转移。

IF 8.2 2区 生物学 Q1 CELL BIOLOGY
Xing Wan, Feng Li, Zhigui Li, Liming Zhou
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引用次数: 0

摘要

酸性微环境是癌症进展的驱动因素之一,其核心机制不清阻碍了新诊断或治疗靶点的发现。ASIC3 是细胞外质子传感器,对酸敏感,但其在结直肠癌酸性肿瘤微环境中的作用尚未见报道。功能分析数据显示,结直肠癌细胞会对特定浓度的乳酸做出反应,加速侵袭和转移,而ASIC3是这一过程中的主要角色。机制揭示了从头脂质合成是ASIC3的调控过程,下调的ASIC3增加并与ACC1和SCD1相互作用,而ACC1和SCD1是从头脂质合成途径中的关键酶,这种相互作用导致不饱和脂肪酸增加,进而诱导EMT促进转移,过表达ASIC3可减少酸性TME增强的结直肠癌转移。结直肠癌的临床样本也显示 ASIC3 表达减少,而 ASIC3 的低表达与结直肠癌的转移和分期有关。本研究首次确定了ASIC3-ACC1/SCD1轴在酸性增强的结直肠癌转移中的作用。ASIC3在结直肠癌中的表达模式与在其他类型癌症中的表达模式明显不同,ASIC3可作为结直肠癌酸性微环境的新型可靠标记物,并可能成为治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ASIC3-activated key enzymes of de novo lipid synthesis supports lactate-driven EMT and the metastasis of colorectal cancer cells.

Acidic microenvironments is a cancer progression driver, unclear core mechanism hinders the discovery of new diagnostic or therapeutic targets. ASIC3 is an extracellular proton sensor and acid-sensitive, but its role in acidic tumor microenvironment of colorectal cancer is not reported. Functional analysis data show that colorectal cancer cells respond to specific concentration of lactate to accelerate invasion and metastasis, and ASIC3 is the main actor in this process. Mechanism reveal de novo lipid synthesis is a regulatory process of ASIC3, down-regulated ASIC3 increases and interacts with ACC1 and SCD1, which are key enzymes in de novo lipid synthesis pathway, this interaction results in increased unsaturated fatty acids, which in turn induce EMT to promote metastasis, and overexpression of ASIC3 reduces acidic TME-enhanced colorectal cancer metastasis. Clinical samples of colorectal cancer also exhibit decreased ASIC3 expression, and low ASIC3 expression is associated with metastasis and stage of colorectal cancer. This study is the first to identify the role of the ASIC3-ACC1/SCD1 axis in acid-enhanced colorectal cancer metastasis. The expression pattern of ASIC3 in colorectal cancer differs significantly from that in other types of cancers, ASIC3 may serve as a novel and reliable marker for acidic microenvironmental in colorectal cancer, and potentially a therapeutic target.

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来源期刊
CiteScore
11.00
自引率
0.00%
发文量
180
期刊介绍: Cell Communication and Signaling (CCS) is a peer-reviewed, open-access scientific journal that focuses on cellular signaling pathways in both normal and pathological conditions. It publishes original research, reviews, and commentaries, welcoming studies that utilize molecular, morphological, biochemical, structural, and cell biology approaches. CCS also encourages interdisciplinary work and innovative models, including in silico, in vitro, and in vivo approaches, to facilitate investigations of cell signaling pathways, networks, and behavior. Starting from January 2019, CCS is proud to announce its affiliation with the International Cell Death Society. The journal now encourages submissions covering all aspects of cell death, including apoptotic and non-apoptotic mechanisms, cell death in model systems, autophagy, clearance of dying cells, and the immunological and pathological consequences of dying cells in the tissue microenvironment.
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