Affiliations 

  • 1 Electronic Marketing and Social Media, Economic and Administrative Sciences, Zarqa University, Zarqa, Jordan. dr_sliman@yahoo.com
  • 2 Medical Engineering Department, Faculty of Engineering, Al-Ahliyya Amman University, Amman, 19328, Jordan
  • 3 Electronic Marketing and Social Media, Economic and Administrative Sciences, Zarqa University, Zarqa, Jordan
  • 4 Department of Chemistry and Biochemistry, School of Sciences, JAIN (Deemed to Be University), Bangalore, Karnataka, India
  • 5 Department of Information Technology, Faculty of Prince Al-Hussein bin Abdullah II of Information Technology, The Hashemite University, Zarqa, Jordan
  • 6 College of Pharmacy, the Islamic University, Najaf, Iraq
  • 7 Centre for Research Impact & Outcome, Chitkara University Institute of Engineering and Technology, Chitkara University, Rajpura, 140401, Punjab, India
  • 8 Department of Chemistry, Sathyabama Institute of Science and Technology, Chennai, Tamil Nadu, India
  • 9 Department of Pharmaceutical Sciences, Siksha 'O' Anusandhan (Deemed to Be University), Bhubaneswar, Odisha-751030, India
  • 10 Department of Mathematics, Chaudhary Charan Singh University, Meerut, India
Naunyn Schmiedebergs Arch Pharmacol, 2026 Mar;399(5):6165-6188.
PMID: 41288679 DOI: 10.1007/s00210-025-04758-9

Abstract

Macrophage polarization has been known as a critical step in balancing inflammatory responses by creating a balanced plasticity between M1 and M2 macrophages, which act as pro-inflammatory and anti-inflammatory mediators, respectively. Histone deacetylases (HDACs) have been shown to play a vital role in polarization, identifying them as possible contributors and therapeutic targets in metabolic diseases, cancer, inflammatory diseases, and other associated conditions. In this regard, isoform-specific HDAC inhibitors (HDACis) can selectively alter macrophage polarization, thereby overcoming the limitations of pan-HDAC inhibitors and offering therapeutic advantages. Moreover, combining HDAC inhibitors with other therapies has emerged as a promising approach, especially in cancer; however, further studies should determine the specificity of HDAC inhibitors as well as address possible problems in optimizing the bioavailability and reducing off-target effects and cytotoxicity to translate these results into practical therapeutic plans for disorders associated with inflammation.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.