HDAC6: Tumor Progression and Beyond

João Marcos Oliveira-Silva1,2, Leilane Sales de Oliveira1,2, João Vitor Marangoni Tagliéri1

  • 1Human Genetics Laboratory, Institute of Natural Sciences, Federal University of Alfenas (UNIFAL-MG), Alfenas, 37130-001, MG, Brazil.

PubMed

Insights

Histone Deacetylase 6 (HDAC6) is a promising cancer target due to its cytoplasmic role and non-histone targets. HDAC6 inhibitors show potential in treating various cancers and are advancing in clinical trials.

Area of Science:

  • Biochemistry
  • Molecular Biology
  • Oncology

Background:

  • Histone Deacetylase 6 (HDAC6) is unique among HDACs, primarily located in the cytoplasm.
  • It possesses two catalytic domains and a distinct ubiquitin-binding domain.
  • HDAC6 deacetylates non-histone substrates like α-tubulin, HSP90, and cortactin.

Purpose of the Study:

  • To review the structural characteristics of HDAC6.
  • To elucidate the biological functions of HDAC6 in tumor progression.
  • To discuss the therapeutic potential of HDAC6 inhibitors in cancer treatment.

Main Methods:

  • Review of existing literature on HDAC6 structure and function.
  • Analysis of HDAC6's role in key cancer hallmarks.
  • Compilation of data from preclinical and clinical trials of HDAC6 inhibitors.

Main Results:

  • HDAC6 influences tumor invasion, metastasis, angiogenesis, drug resistance, stemness, and immune evasion.
  • Selective HDAC6 inhibitors are being investigated for solid and hematological tumors.
  • Several HDAC6 inhibitors have entered clinical trials with positive preliminary results.

Conclusions:

  • HDAC6 is a significant therapeutic target in oncology.
  • Targeting HDAC6 offers a promising strategy for cancer therapy.
  • Ongoing clinical trials are evaluating the efficacy of HDAC6 inhibitors.

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