HNRNPA2B1的机制洞察:肺癌的全面泛癌分析和功能表征。

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xinjie Kuang , Linghao Wu , Yufan Deng , Hongmei Huang , Yonghui Yu , Jiachun Lu , Fuman Qiu
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引用次数: 0

摘要

异质核核糖核蛋白A2B1 (HNRNPA2B1)是hnRNPs的a /B亚家族成员,在肿瘤发生中起关键作用,但其表达模式、分子机制和预后意义尚不充分。在这项研究中,我们利用多个公共数据库进行了全面的泛癌症分析,揭示了HNRNPA2B1在大多数肿瘤类型中一致过表达,并与几种恶性肿瘤的不良预后相关。通路富集分析强调了其参与RNA选择性剪接、运输和稳定性,以及促进肿瘤进展的过程。表观遗传学分析发现,基因扩增和选择性剪接是驱动HNRNPA2B1过表达的潜在机制。此外,HNRNPA2B1水平升高导致对包括达沙替尼在内的多种化疗药物产生耐药性。功能研究表明,HNRNPA2B1通过上调TARDBP和细胞周期相关基因来促进肺癌细胞的增殖和迁移,其中m6A修饰是一个关键的调控机制。总之,这些发现确立了HNRNPA2B1作为多种癌症类型的致癌因子,强调了其作为预后标志物和有希望的治疗靶点的价值,特别是在肺癌中,为靶向治疗策略提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanistic insights into HNRNPA2B1: A comprehensive pan-cancer analysis and functional characterization in lung cancer
Heterogeneous nuclear ribonucleoprotein A2B1 (HNRNPA2B1), a member of the A/B subfamily of hnRNPs, plays a critical role in tumorigenesis, yet its expression patterns, molecular mechanisms, and prognostic significance remain inadequately characterized. In this study, we performed a comprehensive pan-cancer analysis utilizing multiple public databases, revealing that HNRNPA2B1 is consistently overexpressed in most tumor types and correlates with poor prognosis across several malignancies. Pathway enrichment analysis highlighted its involvement in RNA alternative splicing, transport, and stability, processes that contribute to tumor progression. Epigenetic analyses identified gene amplification and alternative splicing as potential mechanisms driving HNRNPA2B1 overexpression. Furthermore, elevated HNRNPA2B1 levels conferred resistance to multiple chemotherapeutics, including Dasatinib. Functional studies demonstrated that HNRNPA2B1 enhances lung cancer cell proliferation and migration by upregulating TARDBP and cell cycle-related genes, with m6A modification serving as a critical regulatory mechanism. Collectively, these findings establish HNRNPA2B1 as an oncogenic factor across multiple cancer types, underscoring its value as a prognostic marker and a promising therapeutic target, particularly in lung cancer, offering new insights for targeted therapeutic strategies.
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来源期刊
CiteScore
12.30
自引率
0.00%
发文量
218
审稿时长
32 days
期刊介绍: BBA Molecular Basis of Disease addresses the biochemistry and molecular genetics of disease processes and models of human disease. This journal covers aspects of aging, cancer, metabolic-, neurological-, and immunological-based disease. Manuscripts focused on using animal models to elucidate biochemical and mechanistic insight in each of these conditions, are particularly encouraged. Manuscripts should emphasize the underlying mechanisms of disease pathways and provide novel contributions to the understanding and/or treatment of these disorders. Highly descriptive and method development submissions may be declined without full review. The submission of uninvited reviews to BBA - Molecular Basis of Disease is strongly discouraged, and any such uninvited review should be accompanied by a coverletter outlining the compelling reasons why the review should be considered.
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