Cited by 55Epigenetics and DNA MethylationChromatin Remodeling and CancerAcute Myeloid Leukemia Research

Polycomb repressive complexes in hematological malignancies

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Iwama, Atsushi·2017·Blood

Abstract

The deregulation of polycomb repressive complexes (PRCs) has been reported in a number of hematological malignancies. These complexes exert oncogenic or tumor-suppressive functions depending on tumor type. These findings have revolutionized our understanding of the pathophysiology of hematological malignancies and the impact of deregulated epigenomes in tumor development and progression. The therapeutic targeting of PRCs is currently attracting increasing attention and being extensively examined in clinical studies, leading to new therapeutic strategies that may improve the outcomes of patients with hematological malignancies.

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Crossref · 10.1182/blood-2017-02-739490

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Authors
Iwama, A.
Affiliations
Chiba University (JP)
Corresponding author
Iwama, Atsushi
Venue
Blood
Published
2017-07-06
Volume
130
Issue
1
Pages
23-29
ISSN
  • 0006-4971 (ISSN-L)
  • 1528-0020
OpenAlex
W2613020405
Cited by
55
References
96
Citations by year
2026: 5 · 2025: 4 · 2024: 2 · 2023: 4 · 2022: 2 · 2021: 6 · 2020: 9 · 2019: 9 · 2018: 12 · 2017: 1 · 2016: 1
FWCI
0.79
Type
journal article
Language
en
Open access
Locations
  • Blood (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Ministry of Education, Culture, Sports, Science and Technology (#25115002, 15H02544)
  • Japan Society for the Promotion of Science (15H02544, 26115002, 16K15498)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
  • Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
Keywords
polycomb repressive complex, hematologic malignancies, epigenetic dysregulation, tumor suppressor function, oncogenic function, epigenome
MeSH terms
Animals, Humans, Neoplasm Proteins, Gene Expression Regulation, Neoplastic, Hematologic Neoplasms, Epigenesis, Genetic, Polycomb-Group Proteins

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