Scholarlink

Background <p>Gastric cancer (GC) remains a major global health challenge, characterized by high morbidity and mortality rates. Early diagnosis is essential for improving patient outcome. This study aims to develop a diagnostic model based on specific signature genes by investigating the association between double-negative (DN) T cells and GC.</p> Methods <p>A bidirectional Mendelian randomization (MR) analysis was conducted to assess the causal relationship between immune cell phenotypes and GC pathogenesis. Three machine learning (ML) algorithms, combined with logistic regression, were employed to identify featured genes. Real-world cohorts and animal experiments were applied to validate the expression levels of DN T cells and selected model genes. Virtual screening was further performed to identify potential therapeutic candidates.</p> Results <p>DN T cells were identified as significant risk factors for GC. A diagnostic model incorporating four genes—EML4, IL32, FXYD5, and TTC39C—was constructed using ML algorithms and demonstrated high predictive accuracy across multiple clinical cohorts. External validation and experimental analyses confirmed elevated DN T cell levels and increased expression of all model genes in GC tissues, correlating with poor prognosis. Virtual screening identified potential therapeutic compounds with strong binding affinity to target proteins, indicating their potential for GC treatment.</p> Conclusions <p>The study established a novel diagnostic model for GC based on DN T cell signature genes, which shows robust predictive performance and significant clinical benefit. The findings underscore the important role of DN T cells and model genes in GC, providing new insights into early diagnosis and potential therapeutic targets for effective management of GC.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Development and validation of a diagnostic machine learning model for gastric cancer risk based on double-negative T cell-related features

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年1月12日

查看全文
  • Zhijing Yin,
  • Ganghua Zhang,
  • Ziwei Yin,
  • Weina Ma,
  • Jingxin Yang,
  • Wenzhi Deng,
  • Ziyang Feng,
  • Zhanwang Wang,
  • Yi Jin,
  • Yuxing Zhu,
  • Ke Cao

摘要

Background

Gastric cancer (GC) remains a major global health challenge, characterized by high morbidity and mortality rates. Early diagnosis is essential for improving patient outcome. This study aims to develop a diagnostic model based on specific signature genes by investigating the association between double-negative (DN) T cells and GC.

Methods

A bidirectional Mendelian randomization (MR) analysis was conducted to assess the causal relationship between immune cell phenotypes and GC pathogenesis. Three machine learning (ML) algorithms, combined with logistic regression, were employed to identify featured genes. Real-world cohorts and animal experiments were applied to validate the expression levels of DN T cells and selected model genes. Virtual screening was further performed to identify potential therapeutic candidates.

Results

DN T cells were identified as significant risk factors for GC. A diagnostic model incorporating four genes—EML4, IL32, FXYD5, and TTC39C—was constructed using ML algorithms and demonstrated high predictive accuracy across multiple clinical cohorts. External validation and experimental analyses confirmed elevated DN T cell levels and increased expression of all model genes in GC tissues, correlating with poor prognosis. Virtual screening identified potential therapeutic compounds with strong binding affinity to target proteins, indicating their potential for GC treatment.

Conclusions

The study established a novel diagnostic model for GC based on DN T cell signature genes, which shows robust predictive performance and significant clinical benefit. The findings underscore the important role of DN T cells and model genes in GC, providing new insights into early diagnosis and potential therapeutic targets for effective management of GC.