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肺癌进展中α5烟碱型乙酰胆碱受体的研究视角

Perspectives on the α5 nicotinic acetylcholine receptor in lung cancer progression.

作者信息

Cai Jiaying, Wang Jingting, Wang Zengping, Wang Jing, Jia Yanfei, Ma Xiaoli

机构信息

Research Center of Basic Medicine, Central Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.

出版信息

Front Cell Dev Biol. 2025 Mar 12;13:1489958. doi: 10.3389/fcell.2025.1489958. eCollection 2025.

DOI:10.3389/fcell.2025.1489958
PMID:40143965
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11937065/
Abstract

Nicotinic acetylcholine receptors (nAChRs) are widely expressed in a variety of cell types and are involved in multiple physiological regulatory mechanisms in cells, tissues and systems. Increasing evidence suggests that the α5 nicotinic acetylcholine receptor (α5-nAChR), encoded by the CHRNA5 gene, is one of a key mediator involved in lung cancer development and immune responses. Several studies have shown that it is a regulator that stimulates processes via various signaling pathways, including STAT3 in lung cancer. In addition, α5-nAChR has a profound effect on lung immune response through multiple immune-related factor pathways. In this review, we focus on the perspectives on α5-nAChR in lung cancer progression, which indicates that targeting α5-nAChR could provide novel anticancer and immune therapy strategies for lung cancer.

摘要

烟碱型乙酰胆碱受体(nAChRs)广泛表达于多种细胞类型中,并参与细胞、组织和系统中的多种生理调节机制。越来越多的证据表明,由CHRNA5基因编码的α5烟碱型乙酰胆碱受体(α5-nAChR)是参与肺癌发展和免疫反应的关键介质之一。多项研究表明,它是一种通过多种信号通路刺激相关过程的调节因子,包括肺癌中的信号转导和转录激活因子3(STAT3)。此外,α5-nAChR通过多种免疫相关因子途径对肺部免疫反应产生深远影响。在本综述中,我们重点探讨α5-nAChR在肺癌进展中的作用,这表明靶向α5-nAChR可为肺癌提供新的抗癌和免疫治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6cc/11937065/020c001deadd/fcell-13-1489958-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6cc/11937065/020c001deadd/fcell-13-1489958-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6cc/11937065/020c001deadd/fcell-13-1489958-g001.jpg

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本文引用的文献

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Nicotine promotes M2 macrophage polarization through α5-nAChR/SOX2/CSF-1 axis in lung adenocarcinoma.尼古丁通过α5-nAChR/ SOX2/ CSF-1 轴促进肺腺癌中 M2 巨噬细胞极化。
Cancer Immunol Immunother. 2024 Nov 2;74(1):11. doi: 10.1007/s00262-024-03866-4.
2
Genomic and Metagenomic Insights into the Distribution of Nicotine-degrading Enzymes in Human Microbiota.人类微生物群中尼古丁降解酶分布的基因组学和宏基因组学见解
Curr Genomics. 2024 May 31;25(3):226-235. doi: 10.2174/0113892029302230240319042208. Epub 2024 Mar 20.
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Spinosad blocks CHRNA5 mediated EGFR signaling pathway activation to inhibit lung adenocarcinoma proliferation.
斯皮诺菌素通过阻断 CHRNA5 介导的 EGFR 信号通路激活抑制肺腺癌增殖。
Biomed Pharmacother. 2024 Aug;177:117105. doi: 10.1016/j.biopha.2024.117105. Epub 2024 Jul 14.
4
Alpha5 nicotine acetylcholine receptor subunit promotes intrahepatic cholangiocarcinoma metastasis.Alpha5 尼古丁乙酰胆碱受体亚基促进肝内胆管癌转移。
Signal Transduct Target Ther. 2024 Mar 8;9(1):63. doi: 10.1038/s41392-024-01761-z.
5
Gut microbial metabolites reveal diet-dependent metabolic changes induced by nicotine administration.肠道微生物代谢产物揭示了尼古丁给药引起的饮食依赖性代谢变化。
Sci Rep. 2024 Jan 11;14(1):1056. doi: 10.1038/s41598-024-51528-3.
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Ionotropic and metabotropic responses by alpha 7 nicotinic acetylcholine receptors.α7 型烟碱型乙酰胆碱受体的离子型和代谢型反应。
Pharmacol Res. 2023 Nov;197:106975. doi: 10.1016/j.phrs.2023.106975. Epub 2023 Oct 29.
7
CircHERC1 promotes non-small cell lung cancer cell progression by sequestering FOXO1 in the cytoplasm and regulating the miR-142-3p-HMGB1 axis.环状 RNA(circRNA)HERC1 通过将 FOXO1 隔离在细胞质中并调节 miR-142-3p-HMGB1 轴来促进非小细胞肺癌细胞的进展。
Mol Cancer. 2023 Nov 6;22(1):179. doi: 10.1186/s12943-023-01888-7.
8
PLEK2 mediates metastasis and invasion via α5-nAChR activation in nicotine-induced lung adenocarcinoma.PLEK2通过尼古丁诱导的肺腺癌中α5烟碱型乙酰胆碱受体激活介导转移和侵袭。
Mol Carcinog. 2024 Feb;63(2):253-265. doi: 10.1002/mc.23649. Epub 2023 Nov 3.
9
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Carcinogenesis. 2023 Dec 15;44(10-11):773-784. doi: 10.1093/carcin/bgad061.
10
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