Jin Xie, Xin-Yang Qu, Rui-Min Wu, Jie Liu, Fan Cheng, Yu Zhang, Xu-Sheng Liu
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Furthermore, functional enrichment analysis was conducted to explore the biological pathways involved, alongside promoter methylation and mutation analyses, to elucidate its regulatory mechanisms. TNNT1 protein levels were analyzed through immunohistochemistry (IHC) on tissue microarray (TMA) sections.</p><p><strong>Results: </strong>Our findings demonstrate that TNNT1 is significantly overexpressed in tumor tissues compared to normal tissues, with elevated expression levels correlating with poor prognosis specifically in colon adenocarcinoma (COAD), liver hepatocellular carcinoma and pancreatic adenocarcinoma. Functional analyses indicated that TNNT1 is involved in tumor aggressiveness-related processes such as epidermal development and keratinization. Notably, TNNT1 expression was linked to immune cell infiltration patterns, highlighting its potential role in modulating the tumor immune microenvironment. IHC analysis revealed significantly higher TNNT1 levels in COAD and rectum adenocarcinoma tissues compared to control samples.</p><p><strong>Conclusion: </strong>This study underscores the potential of TNNT1 as a prognostic biomarker and therapeutic target in digestive system tumors. Our findings pave the way for future research aimed at elucidating the intricate mechanisms underlying TNNT1's roles in tumor biology and its therapeutic implications in improving patient outcomes.</p>","PeriodicalId":10366,"journal":{"name":"Clinical Epigenetics","volume":"17 1","pages":"115"},"PeriodicalIF":4.8000,"publicationDate":"2025-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12232061/pdf/","citationCount":"0","resultStr":"{\"title\":\"Epigenetic regulation of TNNT1 in gastrointestinal cancers prognostic implications and clinical significance.\",\"authors\":\"Jin Xie, Xin-Yang Qu, Rui-Min Wu, Jie Liu, Fan Cheng, Yu Zhang, Xu-Sheng Liu\",\"doi\":\"10.1186/s13148-025-01928-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>This study aims to investigate the expression profile and clinical significance of the Troponin T Type 1 (TNNT1) gene across various digestive system tumors. 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引用次数: 0
摘要
目的:探讨肌钙蛋白T型1 (TNNT1)基因在不同消化系统肿瘤中的表达谱及临床意义。通过阐明TNNT1在肿瘤进展中的作用,我们希望确定其作为预后生物标志物和治疗靶点的潜力。方法:利用癌症基因组图谱(TCGA)和gene expression Omnibus (GEO)数据库的数据,采用生物信息学分析,包括差异基因表达分析和生存分析,评估TNNT1的表达水平。通过Cox回归分析评估TNNT1表达对患者预后的影响。此外,我们还进行了功能富集分析来探索其生物学途径,以及启动子甲基化和突变分析,以阐明其调控机制。通过组织芯片(TMA)切片的免疫组化(IHC)分析TNNT1蛋白水平。结果:我们的研究结果表明,与正常组织相比,TNNT1在肿瘤组织中明显过表达,表达水平升高与预后不良相关,特别是在结肠腺癌(COAD)、肝细胞癌和胰腺腺癌中。功能分析表明,TNNT1参与肿瘤侵袭性相关过程,如表皮发育和角化。值得注意的是,TNNT1表达与免疫细胞浸润模式有关,突出了其在调节肿瘤免疫微环境中的潜在作用。免疫组化分析显示,与对照样本相比,COAD和直肠腺癌组织中TNNT1水平显著升高。结论:本研究强调了TNNT1作为消化系统肿瘤预后生物标志物和治疗靶点的潜力。我们的发现为未来的研究铺平了道路,旨在阐明TNNT1在肿瘤生物学中的作用及其在改善患者预后方面的治疗意义的复杂机制。
Epigenetic regulation of TNNT1 in gastrointestinal cancers prognostic implications and clinical significance.
Objectives: This study aims to investigate the expression profile and clinical significance of the Troponin T Type 1 (TNNT1) gene across various digestive system tumors. By elucidating the role of TNNT1 in tumor progression, we hope to establish its potential as a prognostic biomarker and therapeutic target.
Methods: We assessed the expression levels of TNNT1 by employing bioinformatics analyses, including differential gene expression analysis and survival analysis utilizing data from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases. The impact of TNNT1 expression on patient prognosis was evaluated through Cox regression analyses. Furthermore, functional enrichment analysis was conducted to explore the biological pathways involved, alongside promoter methylation and mutation analyses, to elucidate its regulatory mechanisms. TNNT1 protein levels were analyzed through immunohistochemistry (IHC) on tissue microarray (TMA) sections.
Results: Our findings demonstrate that TNNT1 is significantly overexpressed in tumor tissues compared to normal tissues, with elevated expression levels correlating with poor prognosis specifically in colon adenocarcinoma (COAD), liver hepatocellular carcinoma and pancreatic adenocarcinoma. Functional analyses indicated that TNNT1 is involved in tumor aggressiveness-related processes such as epidermal development and keratinization. Notably, TNNT1 expression was linked to immune cell infiltration patterns, highlighting its potential role in modulating the tumor immune microenvironment. IHC analysis revealed significantly higher TNNT1 levels in COAD and rectum adenocarcinoma tissues compared to control samples.
Conclusion: This study underscores the potential of TNNT1 as a prognostic biomarker and therapeutic target in digestive system tumors. Our findings pave the way for future research aimed at elucidating the intricate mechanisms underlying TNNT1's roles in tumor biology and its therapeutic implications in improving patient outcomes.
期刊介绍:
Clinical Epigenetics, the official journal of the Clinical Epigenetics Society, is an open access, peer-reviewed journal that encompasses all aspects of epigenetic principles and mechanisms in relation to human disease, diagnosis and therapy. Clinical trials and research in disease model organisms are particularly welcome.