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. 2022 Oct 8;12(10):1672.
doi: 10.3390/jpm12101672.

Clinical Significance of the Histone Deacetylase 2 (HDAC-2) Expression in Human Breast Cancer

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Clinical Significance of the Histone Deacetylase 2 (HDAC-2) Expression in Human Breast Cancer

Nikolaos Garmpis et al. J Pers Med. .

Abstract

Background/aim: There is a strong association between malignancy and histone deacetylases (HDACs). Histone deacetylase inhibitors (HDACIs) are now being tested as antitumor agents in various clinical trials. We aimed to assess the clinical importance of HDAC-2 in breast cancer (BC).

Materials and methods: A total of 118 BC specimens were examined immunohistochemically. A statistical analysis was conducted in order to examine the relation between HDAC-2 and the clinicopathological features and survival of the patients.

Results: Higher HDAC-2 expression was related to lobular histological type of cancer, grade III, and stage III BC. In addition, the disease-free period and overall survival were curtailed and negatively related to the over-expression of HDAC-2. Other factors correlating with worse survival were histological types other than ductal or lobular, and the stage of the disease.

Conclusions: This study showed a relationship between HDAC-2 and BC. Further studies are required in order to eventually potentiate the role of HDACIs as anticancer agents in BC.

Keywords: HDAC; breast; cancer; clinicopathological; deacetylase; histone.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Histone deacetylases’ function and classification.
Scheme 1
Scheme 1
Patient selection criteria and flow chart of the current study.
Figure 2
Figure 2
HDAC-2 immunohistochemical expression in breast cancer tissue (×400). (A): Negative nuclear staining. (B): Mild to moderate nuclear staining. (C): Strong nuclear staining.
Figure 3
Figure 3
Kaplan–Meier estimates for survival according to HDAC-2 immunohistochemical expression. (A): Disease-free survival. (B): Overall survival.

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References

    1. Allfrey V.G., Faulkner R., Mirsky A.E. Acetylation and methylation of histones and their possible role in the regulation of RNA synthesis. Proc. Natl. Acad. Sci. USA. 1964;51:786–794. doi: 10.1073/pnas.51.5.786. - DOI - PMC - PubMed
    1. Grunstein M. Histone acetylation in chromatin structure and transcription. Nature. 1997;389:349–352. doi: 10.1038/38664. - DOI - PubMed
    1. Haberland M., Montgomery R.L., Olson E.N. The many roles of histone deacetylases in development and physiology: Implications for disease and therapy. Nat. Rev. Genet. 2009;10:32–42. doi: 10.1038/nrg2485. - DOI - PMC - PubMed
    1. Trapp J., Jung M. The role of NAD+ dependent histone deacetylases (sirtuins) in ageing. Curr. Drug Targets. 2006;7:1553–1560. doi: 10.2174/1389450110607011553. - DOI - PubMed
    1. Garmpi A., Garmpis N., Damaskos C., Valsami S., Spartalis E., Lavaris A., Patelis N., Margonis G.A., Apostolou K.G., Spartalis M., et al. Histone deacetylase inhibitors as a new anticancer option: How far can we go with expectations? J. BUON. 2018;23:846–861. - PubMed

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