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PMID: 23723299 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

HMGB1 in cancer: good, bad, or both?

Kang R, Zhang Q, Zeh HJ, Lotze MT, Tang D

Abstract

Forty years ago, high mobility group box 1 (HMGB1) was discovered in calf thymus and named according to its electrophoretic mobility in polyacrylamide gels. Now, we know that HMGB1 performs dual functions. Inside the cell, HMGB1 is a highly conserved chromosomal protein acting as a DNA chaperone. Outside of the cell, HMGB1 is a prototypical damage-associated molecular pattern, acting with cytokines, chemokines, and growth factors. During tumor development and in cancer therapy, HMGB1 has been reported to play paradoxical roles in promoting both cell survival and death by regulating multiple signaling pathways, including inflammation, immunity, genome stability, proliferation, metastasis, metabolism, apoptosis, and autophagy. Here, we review the current knowledge of both HMGB1's oncogenic and tumor-suppressive roles and the potential strategies that target HMGB1 for the prevention and treatment of cancer.

MeSH Terms
Apoptosis/genetics Autophagy/genetics Cell Nucleus/metabolism Cell Survival/genetics Chemokines/metabolism Cytokines/metabolism HMGB1 Protein/genetics,metabolism Humans Intercellular Signaling Peptides and Proteins/metabolism Neoplasms/genetics,pathology,therapy Signal Transduction/genetics
Chemicals
Chemokines Cytokines HMGB1 Protein HMGB1 protein, human Intercellular Signaling Peptides and Proteins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Kang Rui
Department of Surgery, University of Pittsburgh Cancer Institute, Hillman Cancer Center, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Zhang Qiuhong
Zeh Herbert J
Lotze Michael T
Tang Daolin
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Article Info
Journal
Clinical cancer research : an official journal of the American Association for Cancer Research
Abbr.
Clin Cancer Res
ISSN
1557-3265
Published
2013-08-01
Epub
2013-00-30
Pages
4046-57
Language
English
Region
United States
NLM ID
9502500
PMCID
PMC3732559
Subset
IM
Grants
NCI NIH HHS · R01 CA160417 · United States
NCATS NIH HHS · UL1 TR000005 · United States
NCI NIH HHS · R01CA160417 · United States
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