4.6 Review

DNA Methylation as a Diagnostic Biomarker for Malignant Mesothelioma: A Systematic Review and Meta-Analysis

期刊

JOURNAL OF THORACIC ONCOLOGY
卷 16, 期 9, 页码 1461-1478

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jtho.2021.05.015

关键词

Mesothelioma; Epigenetics; DNA methylation; Biomarker

资金

  1. Stichting tegen Kanker (Foun-dation against Cancer) [FAF-FA/2016/818]
  2. Kom op tegen Kanker (Stand up to Cancer)
  3. Flemish Cancer Society

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This study provides a systematic review of the research investigating DNA methylation in mesothelioma, identifying APC, miR-34b/c, and WIF1 as the most suitable candidate biomarkers. Further research on genome-wide DNA methylation profiling is needed for potential clinical applications.
Malignant mesothelioma is an aggressive cancer type linked to asbestos exposure. Because of several intrinsic challenges, mesothelioma is often diagnosed in an advanced disease stage. Therefore, there is a need for diagnostic biomarkers that may contribute to early detection. Recently, the epigenome of tumors is being extensively investigated to identify biomarkers. This manuscript is a systematic review summarizing the state-of-the-art research investigating DNA methylation in mesothelioma. Four literature databases (PubMed, Scopus, Web of Science, MEDLINE) were systematically searched for studies investigating DNA methylation in mesothelioma up to October 16, 2020. A meta-analysis was performed per gene investigated in at least two independent studies. A total of 53 studies investigated DNA methylation of 97 genes in mesothelioma and are described in a qualitative overview. Furthermore, ten studies investigating 13 genes (APC, CDH1, CDKN2A, DAPK, ESR1, MGMT, miR-34b/c, PGR, RAR beta, RASSF1, SFRP1, SFRP4, WIF1) were included in the quantitative meta-analysis. In this meta-analysis, the APC gene is significantly hypomethylated in mesothelioma, whereas CDH1, ESR1, miR-34b/c, PGR, RAR beta, SFRP1, and WIF1 are significantly hypermethylated in mesothelioma. The three genes that are the most appropriate candidate biomarkers from this metaanalysis are APC, miR-34b/c, and WIF1. Nevertheless, both study number and study objects comprised in this metaanalysis are too low to draw final conclusions on their clinical applications. The elucidation of the genome-wide DNA methylation profile of mesothelioma is desirable in the future, using a standardized genome-wide methylation analysis approach. The most informative CpG sites from this signature could then form the basis of a panel of highly sensitive and specific biomarkers that can be used for the diagnosis of mesothelioma and even for the screening of an at high-risk population of asbestos-exposed individuals. (C) 2021 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.

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