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基因组分析确定TJP3为口腔鳞状细胞癌放疗和放化疗的预后标志物。

Genomic analysis identifies TJP3 as a prognostic marker for radiotherapy and chemoradiotherapy in oral squamous cell carcinoma.

作者信息

Kuk Su Kyung, Lee Jae Il, Lee Jong-Ho, Kwon Ik-Jae, Pang Kang Mi

机构信息

Division of Biomedical Informatics, College of Medicine, Seoul National University, 101 Daehak-ro, Jongno-gu, Seoul, 03080, Republic of Korea.

Department of Oral Pathology, School of Dentistry, Seoul National University, 101 Daehak-ro, Jongno-gu, Seoul, 03080, Republic of Korea.

出版信息

Sci Rep. 2025 Aug 21;15(1):30778. doi: 10.1038/s41598-025-05025-w.

Abstract

This study analyzed somatic mutations and differentially expressed genes in primary oral squamous cell carcinoma (OSCC) tumors to identify prognostic markers for radiotherapy (RT) and concurrent chemo-radiation therapy (CCRT). We used longitudinal whole-exome sequencing (WES) data from a patient who developed radiation-induced sarcoma (RIS) after CCRT with public datasets (TCGA and GSE41613) to identify genes associated with 24-month overall survival (OS). Candidates were further refined using Cox regression for OS. Twenty-two prognostic genes were identified and validated in WES data, functioning as indicators of RT and CCRT resistance. In patients with poor outcomes within 24 months post-RT, CLTCL1, RGL3 and H3C12 showed significant prognostic value in multivariate Cox analyses, while SLC35G5, GARS1 and JPH3 were identified as prognostic markers for CCRT. Limited overlap was observed between RT and CCRT, with TJP3 being the only common gene. RNA-seq data from the GSE217645 revealed that TJP3 exhibited significantly altered expression between radiosensitive and radioresistant cell lines (p = 0.037). RT-related genes were predominantly found in primary tumors, whereas CCRT-related genes were distributed across primary tumor, inflamed granulation tissue, inflammatory myofibroblastic proliferation and RIS. These findings provide insights into molecular mechanisms underlying RT and CCRT resistance, supporting future directions in precision medicine.

摘要

本研究分析了原发性口腔鳞状细胞癌(OSCC)肿瘤中的体细胞突变和差异表达基因,以确定放疗(RT)和同步放化疗(CCRT)的预后标志物。我们使用了一名在CCRT后发生放射性肉瘤(RIS)患者的纵向全外显子测序(WES)数据,并结合公共数据集(TCGA和GSE41613)来识别与24个月总生存期(OS)相关的基因。通过Cox回归对OS进一步筛选候选基因。在WES数据中鉴定并验证了22个预后基因,它们可作为RT和CCRT耐药性的指标。在放疗后24个月内预后较差的患者中,CLTCL1、RGL3和H3C12在多变量Cox分析中显示出显著的预后价值,而SLC35G5、GARS1和JPH3被确定为CCRT的预后标志物。RT和CCRT之间观察到有限的重叠,TJP3是唯一的共同基因。来自GSE217645的RNA测序数据显示,TJP3在放射敏感和放射抗性细胞系之间表现出显著改变的表达(p = 0.037)。RT相关基因主要在原发性肿瘤中发现,而CCRT相关基因分布在原发性肿瘤、炎性肉芽组织、炎性肌成纤维细胞增殖和RIS中。这些发现为RT和CCRT耐药的分子机制提供了见解,为精准医学的未来方向提供了支持。

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