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X连锁肿瘤抑制因子TSPX调节参与表皮生长因子受体(EGFR)信号通路和细胞活力的基因以抑制肺腺癌。

The X-Linked Tumor Suppressor TSPX Regulates Genes Involved in the EGFR Signaling Pathway and Cell Viability to Suppress Lung Adenocarcinoma.

作者信息

Kido Tatsuo, Kong Hui, Lau Yun-Fai Chris

机构信息

Division of Cell and Developmental Genetics, Department of Medicine, Veterans Affairs Medical Center, and the Institute for Human Genetics, University of California, San Francisco, CA 94121, USA.

出版信息

Genes (Basel). 2025 Jan 11;16(1):75. doi: 10.3390/genes16010075.

Abstract

TSPX is an X-linked tumor suppressor that was initially identified in non-small cell lung cancer (NSCLC) cell lines. However, its expression patterns and downstream mechanisms in NSCLC remain unclear. This study aims to investigate the functions of TSPX in NSCLC by identifying its potential downstream targets and their correlation with clinical outcomes. : RNA-seq transcriptome and pathway enrichment analyses were conducted on the TSPX-overexpressing NSCLC cell lines, A549 and SK-MES-1, originating from lung adenocarcinoma and squamous cell carcinoma subtypes, respectively. In addition, comparative analyses were performed using the data from clinical NSCLC specimens (515 lung adenocarcinomas and 502 lung squamous cell carcinomas) in the Cancer Genome Atlas (TCGA) database. : TCGA data analysis revealed significant downregulation of TSPX in NSCLC tumors compared to adjacent non-cancerous tissues (Wilcoxon matched pairs signed rank test < 0.0001). Notably, the TSPX expression levels were inversely correlated with the cancer stage, and higher TSPX levels were associated with better clinical outcomes and improved survival in lung adenocarcinoma, a subtype of NSCLC (median survival extended by 510 days; log-rank test, = 0.0025). RNA-seq analysis of the TSPX-overexpressing NSCLC cell lines revealed that TSPX regulates various genes involved in the cancer-related signaling pathways and cell viability, consistent with the suppression of cell proliferation in cell culture assays. Notably, various potential downstream targets of TSPX that correlated with patient survival (log-rank test, = 0.016 to 4.3 × 10) were identified, including EGFR pathway-related genes , , , and , which were downregulated. : Our results suggest that TSPX plays a critical role in suppressing NSCLC progression by downregulating pro-oncogenic genes, particularly those in the EGFR signaling pathway, and upregulating the tumor suppressors, especially in lung adenocarcinoma. These findings suggest that TSPX is a potential biomarker and therapeutic target for NSCLC management.

摘要

TSPX是一种X连锁肿瘤抑制因子,最初在非小细胞肺癌(NSCLC)细胞系中被鉴定出来。然而,其在NSCLC中的表达模式和下游机制仍不清楚。本研究旨在通过鉴定其潜在的下游靶点及其与临床结局的相关性,来研究TSPX在NSCLC中的功能。对分别源自肺腺癌和肺鳞癌亚型的TSPX过表达NSCLC细胞系A549和SK-MES-1进行了RNA测序转录组和通路富集分析。此外,使用癌症基因组图谱(TCGA)数据库中临床NSCLC标本(515例肺腺癌和502例肺鳞癌)的数据进行了比较分析。TCGA数据分析显示,与相邻非癌组织相比,NSCLC肿瘤中TSPX显著下调(Wilcoxon配对符号秩检验<0.0001)。值得注意的是,TSPX表达水平与癌症分期呈负相关,较高的TSPX水平与更好的临床结局以及NSCLC亚型肺腺癌的生存期改善相关(中位生存期延长510天;对数秩检验,P = 0.0025)。对TSPX过表达NSCLC细胞系的RNA测序分析表明,TSPX调节参与癌症相关信号通路和细胞活力的各种基因,这与细胞培养试验中细胞增殖的抑制一致。值得注意的是,鉴定出了与患者生存相关的TSPX的各种潜在下游靶点(对数秩检验,P = 0.016至4.3×10),包括EGFR通路相关基因,这些基因被下调。我们的结果表明,TSPX通过下调促癌基因,特别是EGFR信号通路中的基因,并上调肿瘤抑制因子,在抑制NSCLC进展中起关键作用,尤其是在肺腺癌中。这些发现表明,TSPX是NSCLC治疗的潜在生物标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2055/11764513/51500ae7133d/genes-16-00075-g001.jpg

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