Histone Deacetylase Inhibitors and Anaplastic Thyroid Carcinoma

Anticancer Res. 2019 Mar;39(3):1119-1127. doi: 10.21873/anticanres.13220.

Abstract

Background/aim: Anaplastic thyroid cancer (ATC) is one of the most aggressive human malignancies, remaining generally incurable. Histone deacetylase (HDAC) seems to play a role in regulating transcription of genes involved in ATC, making HDAC inhibitors (HDACI) promising anticancer drugs for ATC. The purpose of this review was to evaluate the role of HDACIs in ATC treatment and describe the latest trends of current research on this field.

Materials and methods: This literature review was performed using the MEDLINE database. The keywords/phrases were; thyroid cancer, anaplastic, HDAC, histone, deacetylase*, HDACI.

Results: Compounds, such as SuberoylAnilide Hydroxamic Acid, valproic acid, sodium butyrate, butyrate, phenylbutyrate, trichostatin A, AB1-13, panobinostat or LBH589, belinostat, MS-275, depsipeptide, CUDC101, CUDC907, N-Hydroxy-7-(2-naphthylthio)-Hepanomide (HNHA), and PXD101 have shown promising antitumor effects against ATC.

Conclusion: HDACIs represent a promising therapy for ATC management, both as monotherapy and in combination with other anticancer drugs.

Keywords: HDAC; anaplastic; cancer; histone deacetylase inhibitors; review; thyroid.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • Histone Deacetylase Inhibitors / therapeutic use*
  • Humans
  • Thyroid Carcinoma, Anaplastic / drug therapy*
  • Thyroid Neoplasms / drug therapy*

Substances

  • Antineoplastic Agents
  • Histone Deacetylase Inhibitors