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Association between Atopic Dermatitis and Colorectal Cancer: TET2 as a Shared Gene Signature and Prognostic Biomarker.
Zhan, Zhi-Qing; Huang, Ze-Min; Zeng, Rui-Qi; Luo, Yu-Hua; Xie, Zhi-Xin; Chen, Ying-Zhou; Chen, Pei-Zhen; Luo, Tian-Ye; Sun, Baoqing; Cheng, Zhangkai J.
Afiliação
  • Zhan ZQ; Department of Clinical Laboratory, National Center for Respiratory Medicine, National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Med
  • Huang ZM; Division of Gastroenterology and Hepatology; Shanghai Institute of Digestive Disease; NHC Key Laboratory of Digestive Diseases; State Key Laboratory for Oncogenes and Related Genes; Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
  • Zeng RQ; Department of Clinical Medicine, Guangzhou Medical University, Guangzhou, China.
  • Luo YH; Department of Clinical Medicine, Guangzhou Medical University, Guangzhou, China.
  • Xie ZX; Department of Clinical Medicine, Guangzhou Medical University, Guangzhou, China.
  • Chen YZ; Department of Clinical Medicine, Guangzhou Medical University, Guangzhou, China.
  • Chen PZ; Department of Gastroenterology and Hepatology, West China Hospital, Sichuan University, China.
  • Luo TY; Department of Clinical Medicine, Guangzhou Medical University, Guangzhou, China.
  • Sun B; Department of Clinical Medicine, Guangzhou Medical University, Guangzhou, China.
  • Cheng ZJ; Department of Clinical Laboratory, National Center for Respiratory Medicine, National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Med
J Cancer ; 15(5): 1414-1428, 2024.
Article em En | MEDLINE | ID: mdl-38356721
ABSTRACT

Background:

Recent studies have linked atopic dermatitis (AD) to colorectal cancer (CRC) risk. Their causality and potential molecular mechanisms remain unclear.

Methods:

We performed Mendelian randomization (MR) analysis to evaluate the causality between AD and CRC. Summary statistic data-based Mendelian randomization (SMR) analysis was used to identify CRC-related causal genes. Transcriptome analyses and immunohistochemical methods were applied to investigate the shared gene signature and potential mechanisms that contribute to the pathogenesis of both AD and CRC. A predictive analysis was performed to examine the shared gene signature associated with immunotherapy response in CRC.

Results:

MR analysis indicated a causal association between AD and a decreased risk of CRC. SMR analysis uncovered TET2 as a CRC-related causal gene, showing an inverse relationship with the risk of CRC. Transcriptome analyses identified TET2 as a shared gene signature between AD and CRC. Decreased TET2 expression is associated with impaired demethylation and worse prognosis in CRC patients. We observed ten pathways related to the inflammatory response and immune regulation that may be shared mechanisms underlying both AD and CRC. These findings were validated through single-cell analysis. TET2 shows promise as a powerful predictive biomarker for cancer prognosis and immunotherapy response in CRC.

Conclusion:

There is a causal association between AD and a decreased risk of CRC. AD may influence the occurrence of CRC by modulating immune and inflammatory responses. TET2 could serve as a potential biomarker for prognosis and may be considered a novel therapeutic target for methylation and immune-related interventions.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Cancer Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Cancer Ano de publicação: 2024 Tipo de documento: Article