Critical role of the high mobility group A proteins in hematological malignancies.

Hematol Oncol

Department of Molecular Medicine and Medical Biotechnology (DMMBM), National Research Council (CNR), Institute for Experimental Endocrinology and Oncology (IEOS) "G. Salvatore", University of Naples "Federico II", Naples, Italy.

Published: February 2022

AI Article Synopsis

  • The HMGA protein family consists of non-histone chromatin remodeling proteins that function as architectural transcriptional factors and regulate gene expression by binding to DNA.
  • HMGA proteins are crucial during embryogenesis and have been implicated in various human cancers, particularly in hematological malignancies where they are often overexpressed and associated with poor survival.
  • Recent research indicates a potential therapeutic target by inhibiting both HMGA and EZH2 proteins in diffuse B-cell lymphomas, suggesting a novel approach to treatment.

Article Abstract

The high mobility group A (HMGA) protein family is composed of three non-histone chromatin remodeling proteins that act as architectural transcriptional factors. Indeed, although HMGA proteins lack transcriptional activity per se, they bind the minor groove of DNA at AT-rich sequences, and, interacting with the transcription machinery, are able to modify chromatin modeling, thus regulating the expression of several genes. HMGA proteins have been deeply involved in embryogenesis process, and a large volume of studies has pointed out their key role in human cancer. Here, we review the studies on the role of the HMGA proteins in human hematological malignancies: they are overexpressed in most of the cases and their expression correlates with a reduced survival. In some cases, such as in acute lymphoblastic leukemia and acute myelogenous leukemia, HMGA2 gene rearrangements have been also described. Finally, recent studies evidence a synergism between HMGA and EZH2 in diffuse B-cell lymphomas, suggesting an innovative therapy for this disease based on the inhibition of the function of both these proteins.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293314PMC
http://dx.doi.org/10.1002/hon.2934DOI Listing

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