Scholarlink

Background <p>To investigate the role and mechanism of the transcription factor ETS2 in mediating resistance to neoadjuvant immunotherapy combined with chemotherapy in esophageal squamous cell carcinoma (ESCC).</p> Methods <p>Single-cell RNA sequencing (scRNA-seq) was performed on tumor tissues from ESCC patients who received neoadjuvant therapy. Integrated analyses were conducted using clinical information, genomic and transcriptomic data from public databases (TCGA) and a single-center patient cohort. Weighted gene co-expression network analysis (WGCNA) was employed to identify senescence-associated gene modules. The association between ETS2 expression and cellular senescence or signaling pathway activity was evaluated using gene set enrichment analysis (GSEA) and computational scoring of senescence-related gene sets.</p> Results <p>ETS2-high epithelial cells were localized at the terminal end of the differentiation trajectory inferred by pseudotime analysis and were enriched in tumors with poor treatment response. ETS2 was highly expressed in ESCC tumor tissues and significantly associated with adverse patient outcomes. Transcriptomic analysis (TCGA) demonstrated significant enrichment of TGF-β in the ETS2-high group. WGCNA identified a senescence-associated “coral” gene module, whose expression was significantly correlated with patient age and induced senescence gene set scores, and exhibited the strongest association with senescence among all modules.</p> Conclusion <p>High expression of ETS2 in ESCC predicts poor prognosis and resistance to neoadjuvant therapy. Its mechanism may involve inducing a senescent state in tumor cells and promoting aggressive tumor behavior through activation of key signaling pathways such as TGF-β. The “coral” module identified by WGCNA represents a critical senescence-related gene signature in ESCC.</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

Single-Cell RNA Sequencing Identifies a Distinct Epithelial Subpopulation Driving Resistance to Neoadjuvant Chemoimmunotherapy in Esophageal Squamous Cell Carcinoma

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年4月17日

查看全文
  • Zuoyu Chen,
  • Xin Yu,
  • Kaili Liu,
  • Yiping Zou,
  • Xue Ding,
  • Xiaolong Zhang,
  • Liangliang Wu,
  • Qiang Song,
  • Hailong Wang

摘要

Background

To investigate the role and mechanism of the transcription factor ETS2 in mediating resistance to neoadjuvant immunotherapy combined with chemotherapy in esophageal squamous cell carcinoma (ESCC).

Methods

Single-cell RNA sequencing (scRNA-seq) was performed on tumor tissues from ESCC patients who received neoadjuvant therapy. Integrated analyses were conducted using clinical information, genomic and transcriptomic data from public databases (TCGA) and a single-center patient cohort. Weighted gene co-expression network analysis (WGCNA) was employed to identify senescence-associated gene modules. The association between ETS2 expression and cellular senescence or signaling pathway activity was evaluated using gene set enrichment analysis (GSEA) and computational scoring of senescence-related gene sets.

Results

ETS2-high epithelial cells were localized at the terminal end of the differentiation trajectory inferred by pseudotime analysis and were enriched in tumors with poor treatment response. ETS2 was highly expressed in ESCC tumor tissues and significantly associated with adverse patient outcomes. Transcriptomic analysis (TCGA) demonstrated significant enrichment of TGF-β in the ETS2-high group. WGCNA identified a senescence-associated “coral” gene module, whose expression was significantly correlated with patient age and induced senescence gene set scores, and exhibited the strongest association with senescence among all modules.

Conclusion

High expression of ETS2 in ESCC predicts poor prognosis and resistance to neoadjuvant therapy. Its mechanism may involve inducing a senescent state in tumor cells and promoting aggressive tumor behavior through activation of key signaling pathways such as TGF-β. The “coral” module identified by WGCNA represents a critical senescence-related gene signature in ESCC.