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Role of HMGB1 and its associated signaling pathways in human malignancies.

Authors :
Idoudi S
Bedhiafi T
Pedersen S
Elahtem M
Alremawi I
Akhtar S
Dermime S
Merhi M
Uddin S
Source :
Cellular signalling [Cell Signal] 2023 Dec; Vol. 112, pp. 110904. Date of Electronic Publication: 2023 Sep 25.
Publication Year :
2023

Abstract

The High-Mobility Group Box-1 (HMGB1), a non-histone chromatin-associated protein, plays a crucial role in cancer growth and response to therapy as it retains a pivotal role in promoting both cell death and survival. HMGB1 has been reported to regulate several signaling pathways engaged in inflammation, genome stability, immune function, cell proliferation, cell autophagy, metabolism, and apoptosis. However, the association between HMGB1 and cancer is complex and its mechanism in tumorigenesis needs to be further elucidated. This review aims to understand the role of HMGB1 in human malignancies and discuss the signaling pathways linked to this process to provide a comprehensive understanding on the association of HMGB1 with carcinogenesis. Further, we will review the role of HMGB1 as a target/biomarker for cancer therapy, the therapeutic strategies used to target this protein, and its potential role in preventing or treating cancers. In light of the recent growing evidence linking HMGB1 to cancer progression, we think that it may be suggested as a novel and emergent therapeutic target for cancer therapy. Hence, HMGB1 warrants paramount investigation to comprehensively map its role in tumorigenesis.<br />Competing Interests: Declaration of Competing Interest The authors declare that this work was conducted in the absence of any financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-3913
Volume :
112
Database :
MEDLINE
Journal :
Cellular signalling
Publication Type :
Academic Journal
Accession number :
37757902
Full Text :
https://doi.org/10.1016/j.cellsig.2023.110904