Evidence map›Paper›PMID 35416406›Full record

ArticleCancer medicine2022

Pan-cancer analysis of mutations in open chromatin regions and their possible association with cancer pathogenesis.

Chie Kikutake, Mikita Suyama

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In one paragraph

Article in Cancer medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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0cells of the map it votes in
6citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. [PINK1 suppresses colorectal cancer cell growth through epigenetic regulation of histone modifications].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2025
    Article
  2. Pan-cancer and multiomics: advanced strategies for diagnosis, prognosis, and therapy in the complex genetic and molecular universe of cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Chie KikutakeMedical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.ORCID 0000-0002-9571-641X
Mikita SuyamaMedical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.ORCID 0000-0001-9526-3193

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOpen chromatin is associated with gene transcription. Previous studies have shown that the density of mutations in open chromatin regions is lower than that in flanking regions because of the higher accessibility of DNA repair machinery. However, in several cancer types, open chromatin regions show an increased local density of mutations in activated regulatory regions. Although the mutation distribution within open chromatin regions in cancer cells has been investigated, only few studies have focused on their functional implications in cancer. To reveal the impact of highly mutated open chromatin regions on cancer, we investigated the association between mutations in open chromatin regions and their possible functions.

methodsWhole-genome sequencing data of 18 cancer types were downloaded from the PanCancer Analysis of Whole Genomes and Catalog of Somatic Mutations in Cancer. We quantified the mutations located in open chromatin regions defined by The Cancer Genome Atlas and classified open chromatin regions into three categories based on the number of mutations. Then, we investigated the chromatin state, amplification, and possible target genes of the open chromatin regions with a high number of mutations. We also analyzed the association between the number of mutations in open chromatin regions and patient prognosis.

resultsIn some cancer types, the proportion of promoter or enhancer chromatin state in open chromatin regions with a high number of mutations was significantly higher than that in the regions with a low number of mutations. The possible target genes of open chromatin regions with a high number of mutations were more strongly associated with cancer than those of other open chromatin regions. Moreover, a high number of mutations in open chromatin regions was significantly associated with a poor prognosis in some cancer types.

conclusionsThese results suggest that highly mutated open chromatin regions play an important role in cancer pathogenesis and can be effectively used to predict patient prognosis.

Indexed as

ChromatinNeoplasmsGenome, HumanHumansMutationPromoter Regions, GeneticChromatinbioinformaticscancer geneticsgenomicsmedical geneticsTCGA

Identifiers

PMID35416406
PMCPMC9582691

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