4.7 Article

Prognostic value of JAK3 promoter methylation and mRNA expression in clear cell renal cell carcinoma

期刊

JOURNAL OF ADVANCED RESEARCH
卷 40, 期 -, 页码 153-166

出版社

ELSEVIER
DOI: 10.1016/j.jare.2021.11.016

关键词

Janus kinase 3; Renal cell carcinoma; Epigenetic biomarker; Tumor immune microenvironment; Tumor immune cell infiltration

资金

  1. National Natural Science Foundation of China
  2. Guangdong Esophageal Cancer Institute Science and Technology Program
  3. [81972569]
  4. [81772925]
  5. [81972623]
  6. [81702761]
  7. [M201802]

向作者/读者索取更多资源

This study investigates the biological and clinical significance of JAK3 promoter methylation in clear cell renal cell carcinoma (ccRCC). The results show that JAK3 promoter is significantly hypomethylated in ccRCC tumor tissues and is strongly correlated with high JAK3 mRNA expression. JAK3 promoter hypomethylation predicts advanced clinicopathological characteristics and shorter overall survival. Furthermore, JAK3 promoter methylation is associated with immune cell infiltration and expression of immune checkpoint molecules. The findings suggest that JAK3 promoter methylation may serve as a molecular biomarker for predicting responses to immune checkpoint inhibitors in ccRCC.
Introduction: Janus kinase 3 (JAK3) is a well-established oncogene in clear cell renal cell carcinoma (ccRCC). The methylation status of oncogene promoters has emerged as biomarkers for cancer diagnosis and prognosis.Objective: This study aims to investigate the biological and clinical significance of JAK3 promoter methy-lation in ccRCC.Methods: We analyzed the relationship of JAK3 promoter methylation with its mRNA expression, overall survival, and immune cell infiltration in a cohort obtained from The Cancer Genome Atlas (TCGA), which was further validated by another independent cohort. We further validated correlations of JAK3 promoter methylation with JAK3 expression, overall survival, and immune cell infiltration in an independent ccRCC cohort (Sun Yat-sen University Cancer Center (SYSUCC) cohort) by methods of immunohistochemistry (IHC) and pyrosequencing.Results: We found JAK3 promoter was significantly hypomethylated in tumor tissues compared to normal adjacent tissues in ccRCC, and JAK3 promoter hypomethylation was strongly correlated with high JAK3 mRNA expression in all three ccRCC cohorts we examined. JAK3 promoter hypomethylation predicted advanced clinicopathological characteristics and shorter overall survival (TCGA cohort and SYSUCC cohort). Furthermore, we found that JAK3 promoter methylation was significantly associated with immune cell infiltration and expression of immune checkpoint molecules (TCGA cohort and CPTAC cohort). Finally, our SYSUCC cohort validated that JAK3 promoter methylation was correlated with CD4' and CD8' T cell infiltration in ccRCC tumor tissues.Conclusion: Our data demonstrated that the crucial role of JAK3 promoter methylation in its expression regulation and tumor microenvironment. JAK3 promoter methylation and expression are associated with clinicopathological characteristics, overall survival, and immune cell infiltration in ccRCC. We propose a rationale for further validation of JAK3 promoter methylation as a molecular biomarker for predicting responses to immune checkpoint inhibitors in ccRCC.(c) 2022 The Authors. Published by Elsevier B.V. on behalf of Cairo University. This is an open access article

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