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尿路上皮癌中作为预后生物标志物的表达与变异的综合分析

Integrative Analysis of Expression and Variants as Prognostic Biomarkers in Urothelial Cancer.

作者信息

Chung Chia-Min, Chang Han, Chang Chao-Hsiang, Chang Yi-Huei, Hsiao Po-Jen, Lien Chi-Shun, Chung Chi-Jung

机构信息

Graduate Institute of Biomedical Sciences, China Medical University, Taichung 404328, Taiwan.

Department of Psychiatry and Center for Addiction and Mental Health, China Medical University Hospital, Taichung 404327, Taiwan.

出版信息

Int J Mol Sci. 2025 Jul 2;26(13):6378. doi: 10.3390/ijms26136378.

Abstract

is a transcription factor involved in urothelial differentiation and is widely used as a diagnostic marker for urothelial carcinoma (UC). Although loss of GATA3 expression has been linked to more aggressive disease, its prognostic significance remains uncertain. Genetic variation within the locus, particularly rs1244159, may influence protein expression and clinical outcomes. We conducted a case control study in Taiwan including 461 UC cases and 586 controls genotyped for four SNPs. GATA3 expression was assessed via immunohistochemistry (IHC) in 98 tumor tissues. Logistic regression and Kaplan-Meier analyses were used to evaluate SNP associations and survival outcomes. An XGBoost-based machine learning model with SHAP (SHapley Additive exPlanations) was applied to rank survival predictors. The rs1244159 G allele was associated with a significantly reduced UC risk (adjusted OR = 0.48, = 0.0231) and higher GATA3 expression ( = 0.0173). High GATA3 expression predicted improved overall survival ( = 0.0092), particularly among G allele carriers ( = 0.0071). SHAP analysis identified age, chemotherapy, and GATA3 expression as the top predictors of survival, consistent with Cox regression results. In conclusion, our integrative analysis suggests that the rs1244159 G allele modulates GATA3 expression and influences UC prognosis. Combining genomics, pathology, and machine learning, may serve as a clinically useful biomarker for risk stratification and outcome prediction in UC.

摘要

是一种参与尿路上皮分化的转录因子,被广泛用作尿路上皮癌(UC)的诊断标志物。尽管GATA3表达缺失与更具侵袭性的疾病有关,但其预后意义仍不确定。该基因座内的基因变异,特别是rs1244159,可能影响蛋白质表达和临床结果。我们在台湾进行了一项病例对照研究,包括461例UC病例和586例对照,对四个单核苷酸多态性(SNP)进行基因分型。通过免疫组织化学(IHC)评估了98个肿瘤组织中的GATA3表达。使用逻辑回归和Kaplan-Meier分析来评估SNP关联和生存结果。应用基于XGBoost的带有SHAP(SHapley加性解释)的机器学习模型对生存预测因子进行排名。rs1244159的G等位基因与UC风险显著降低(调整后的OR = 0.48,P = 0.0231)和更高的GATA3表达(P = 0.0173)相关。高GATA3表达预测总体生存率提高(P = 0.0092),特别是在G等位基因携带者中(P = 0.0071)。SHAP分析确定年龄、化疗和GATA3表达是生存的主要预测因子,与Cox回归结果一致。总之,我们的综合分析表明,rs1244159的G等位基因调节GATA3表达并影响UC预后。结合基因组学、病理学和机器学习,其可能作为UC风险分层和结果预测的临床有用生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7060/12249568/90ad741a1e45/ijms-26-06378-g001.jpg

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