Anti-cancer effects of naturally derived compounds targeting histone deacetylase 6-related pathways

Pharmacol Res. 2018 Mar:129:337-356. doi: 10.1016/j.phrs.2017.11.004. Epub 2017 Nov 11.

Abstract

Alterations of the epigenetic machinery, affecting multiple biological functions, represent a major hallmark enabling the development of tumors. Among epigenetic regulatory proteins, histone deacetylase (HDAC)6 has emerged as an interesting potential therapeutic target towards a variety of diseases including cancer. Accordingly, this isoenzyme regulates many vital cellular regulatory processes and pathways essential to physiological homeostasis, as well as tumor multistep transformation involving initiation, promotion, progression and metastasis. In this review, we will consequently discuss the critical implications of HDAC6 in distinct mechanisms relevant to physiological and cancerous conditions, as well as the anticancer properties of synthetic, natural and natural-derived compounds through the modulation of HDAC6-related pathways.

Keywords: (−)-epigallocatechin-3-gallate (PubChem CID: 65064); 20(S)-Rh2 (PubChem CID: 119307); ACY-1215 (PubChem CID: 53340666); ACY-241 (PubChem CID: 53340426); Cancer hallmarks; Cancer therapy; FK228 (PubChem CID: 5352062); HDAC6; HDAC6 inhibitors; LBH-589 (PubChem CID: 6918837); Natural compounds; PXD101 (PubChem CID: 6918638); SAHA (PubChem CID: 5311); aceroside VIII (PubChem CID: 21637600); butyrate (PubChem CID: 264); curcumin (PubChem CID: 969516); ellagic acid (PubChem CID: 5281855); genistein (PubChem CID: 5280961); salirepol (PubChem CID: 188287); sulforaphane (PubChem CID: 5350); trichostatin A (PubChem CID: 444732); tubacin (PubChem CID: 6675804); tubastatin A (PubChem CID: 49850262); ursodeoxycholic acid (PubChem CID: 31401); ursolic acid (PubChem CID: 64945).

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • Histone Deacetylase 6 / metabolism*
  • Humans
  • Neoplasms / drug therapy*
  • Neoplasms / metabolism
  • Signal Transduction

Substances

  • Antineoplastic Agents
  • Histone Deacetylase 6