Cited by 171Histone Deacetylase Inhibitors ResearchEpigenetics and DNA MethylationGenomics and Chromatin Dynamics

Recent histone deacetylase inhibitors in cancer therapy

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Parveen, Roza, Harihar, Divya, Chatterji, Biswa Prasun·2023·Cancer

Abstract

Cancer metastasis increases the complexity of the disease and escalates patient mortality. Traditional chemotherapy has been associated with low efficacy and marked side effects. Studies pivot toward histone deacetylase (HDAC) enzymes and inhibitors because they are critical for chromatin structure, gene regulation, and cellular activities that are linked to metastasis and cancer progression. HDAC inhibitors (HDACi) can alter gene expression patterns and can lead to cell‐cycle arrest and apoptosis in neoplastic cells. Several HDACi drugs like vorinostat, romidepsin, panobinostat, and belinostat are approved by the Food and Drug Administration. China and Japan have approved the use of tucidinostat, a new subtype‐selective HDACi that inhibits class 1 HDAC1, HDAC2, HDAC3, as well as class 2b HDAC10. These drugs have shown promising results in the treatment of multiple carcinoma including cervical cancer, T‐cell lymphoma, brain cancer, and breast cancer. This review highlights the HDACi classes, the mechanism of action of these inhibitors, their preclinical and clinical efficacy, and the latest clinical trials and patents used in cancer therapeutics. Overall, this review focuses on patents and clinical trials data from 2019 onward to give a better viewpoint on current trends in HDACis as chemotherapy agents.

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  • Various KDAC inhibitors have been approved by the FDA, such as vorinostat and romidepsin, but there are currently no approved KAT inhibitors.

    “Various KDAC inhibitors [19] have been approved by the FDA such as vorinostat [20] (commonly known as SAHA) and romidepsin [21], but there are currently no approved KAT inhibitors [22–24].”

    From Acetylation: a new target for protein degradation in cancer (2025) · cites this paper as [19]

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Research works printed but not linked: 3

  1. Kwon Y, Kim Y, Jung H, Jeoung D. Role of HDAC3-miRNA-CAGE network in anti-cancer drug-resistance. Int J Mol Sci. 2018;20(1): 51. doi:10.3390/ijms2001005 · DOI
  2. Kozloff MF, Berlin J, Flynn PJ, et al Randomized phase II trial of tucidinostat plus FOLFOX in patients with metastatic colorectal cancer refractory to standard therapies. Clin Cancer Res. 2021;27(2): 324-332.
  3. West AC, Johnstone RW, Newbold A. Histone deacetylase in- hibitors: current status and perspectives. Int J Biochem Cell Biol. 2019;116:105642.

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Authors
Parveen, R., Harihar, D., & Chatterji, B. P.
Affiliations
  • Tampere University (FI)
  • KTH Royal Institute of Technology (SE)
  • Assam Down Town University (IN)
Corresponding author
Chatterji, Biswa Prasun
Venue
Cancer
Publisher
Wiley
Published
2023-08-10
Volume
129
Issue
21
Pages
3372-3380
ISSN
  • 0008-543X (ISSN-L)
  • 1097-0142
OpenAlex
W4385716353
Cited by
171
References
47
Citations by year
2026: 62 · 2025: 73 · 2024: 34 · 2023: 2
FWCI
4.51
Type
journal article
Language
en
Open access
Locations
  • Cancer (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Histone Deacetylase Inhibitors Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
Keywords
histone deacetylase inhibitors, cancer therapy, vorinostat, romidepsin, panobinostat, belinostat, tucidinostat, chromatin regulation, apoptosis, cell cycle arrest, metastasis, cervical cancer, T-cell lymphoma, breast cancer, brain cancer, patents, clinical trials
MeSH terms
Animals, Antineoplastic Agents, Clinical Trials as Topic, Humans, Neoplasms, Histone Deacetylase Inhibitors

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