Skip to content
2000
Volume 15, Issue 9
  • ISSN: 1389-5575
  • E-ISSN: 1875-5607

Abstract

Histone Deacetylase (HDAC) is an established and validated target for the treatment of cancer. It has been attempted to present a comprehensive review on the inhibitors for Class-I Histone Deacetylase enzyme family, reported during the period from 2002 to 2012. This review has summarized the inhibitors, based on their specificity towards different isoforms within this class. Further various recent United State (US) patents and the HDAC inhibitors, used singly or in combination undergoing clinical trial as anticancer agents have been reviewed. Three such inhibitors SAHA, Romidepsin and Belinostat have already been approved by the US-FDA for the treatment of cancer.

Loading

Article metrics loading...

/content/journals/mrmc/10.2174/1389557515666150521162237
2015-07-01
2025-12-06
Loading full text...

Full text loading...

/content/journals/mrmc/10.2174/1389557515666150521162237
Loading

  • Article Type:
    Research Article
Keyword(s): cancer; Histone Deacetylase; isoform; Romidepsin; US-FDA
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test