4.5 Review

The progression of HMGB1-induced autophagy in cancer biology

Journal

ONCOTARGETS AND THERAPY
Volume 12, Issue -, Pages 365-377

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/OTT.S185876

Keywords

HMGB1; autophagy; cancer; noncoding RNA; drug resistance

Funding

  1. National Natural Science Foundation of China [81672307, 81871871]
  2. Medical Innovation Team Foundation of the Jiangsu Provincial Enhancement Health Project [CXTDA2017021]
  3. 333 high class Talented Man Project [BRA2016509]

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Autophagy is an important process of cellular degradation and has been proven to contribute to tumorigenesis. High-mobility group box 1 (HMGB1) is an abundant nonhistone protein that has been widely reported to play a central role in the induction of autophagy. In nucleus, HMGB1 upregulates the expression of HSP27 to induce autophagy. In cytoplasm, the Beclin-1/ PI3K-III complex can be activated by HMGB1 to promote autophagy. Extracellular HMGB1 binds to the receptor for advanced glycation end products to induce autophagy. Recent studies have shown that HMGB1-induced autophagy exerts multiple functions in various cancers like proliferation. Moreover, inhibition of HMGB1-induced autophagy can reverse chemoresistance, which is regulated by noncoding RNAs such as microRNAs and lncRNAs. Here, we provide a brief introduction to HMGB1 and HMGB1-induced autophagy in cancer. We also discuss the challenges associated with performing further investigations on this issue. HMGB1-induced autophagy exerts significant functions in cancer and has potential utility for new strategy to reverse drug resistance.

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