Your browser doesn't support javascript.
loading
Polycomb complexes in normal and malignant hematopoiesis.
Di Carlo, Valerio; Mocavini, Ivano; Di Croce, Luciano.
Affiliation
  • Di Carlo V; Centre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona, Spain.
  • Mocavini I; Centre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona, Spain.
  • Di Croce L; Centre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona, Spain luciano.dicroce@crg.eu.
J Cell Biol ; 218(1): 55-69, 2019 01 07.
Article in En | MEDLINE | ID: mdl-30341152
ABSTRACT
Epigenetic mechanisms are crucial for sustaining cell type-specific transcription programs. Among the distinct factors, Polycomb group (PcG) proteins are major negative regulators of gene expression in mammals. These proteins play key roles in regulating the proliferation, self-renewal, and differentiation of stem cells. During hematopoietic differentiation, many PcG proteins are fundamental for proper lineage commitment, as highlighted by the fact that a lack of distinct PcG proteins results in embryonic lethality accompanied by differentiation biases. Correspondingly, proteins of these complexes are frequently dysregulated in hematological diseases. In this review, we present an overview of the role of PcG proteins in normal and malignant hematopoiesis, focusing on the compositional complexity of PcG complexes, and we briefly discuss the ongoing clinical trials for drugs targeting these factors.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hematopoietic Stem Cells / Hematologic Neoplasms / Epigenesis, Genetic / Polycomb-Group Proteins / Hematopoiesis Limits: Animals / Humans Language: En Journal: J Cell Biol Year: 2019 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hematopoietic Stem Cells / Hematologic Neoplasms / Epigenesis, Genetic / Polycomb-Group Proteins / Hematopoiesis Limits: Animals / Humans Language: En Journal: J Cell Biol Year: 2019 Document type: Article Affiliation country:
...