Histone Deacetylase 10 Inhibitors Suppress Progression of Endometriosis via Activation of Interferon Regulatory Factor 6 and Dachshund Homolog 1

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Histone deacetylase 10 inhibitors suppressed endometriotic stromal cell proliferation and induced cell cycle arrest by activating interferon regulatory factor 6 and dachshund homolog 1.

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This study examined how histone deacetylase 10 inhibitors (tucidinostat and TH34) affect proliferation and cell-cycle progression in human endometriotic cyst stromal cells (ECSCs), using assays of cell cycle and RNA sequencing to identify HDAC10 target genes. The authors found that both HDAC10 inhibitors reduced ECSC proliferation and induced G0/G1 cell-cycle arrest, while DACH1 and IRF6 were identified as HDAC10 target genes whose promoters showed increased histone acetylation after treatment. Forced expression of DACH1 and IRF6 in ECSCs was used to confirm their functional roles, and HDAC10Is were linked to acetylated histone accumulation at the DACH1/IRF6 promoter regions. This paper does not explicitly state limitations in the excerpt provided. This paper is centrally about endometriosis — it demonstrates that HDAC10 inhibition suppresses the progression-relevant behaviors of endometriotic cyst stromal cells through IRF6 and DACH1 activation.

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Abstract

AIM: To investigate the mechanisms of histone deacetylase (HDAC) 10 inhibitors (HDAC10Is) action in endometriosis and the target molecules of HDAC10Is. METHODS: We assessed the effects of HDAC10Is, tucidinostat and TH34, on the proliferation and the cell cycle in human endometriotic cyst stromal cells (ECSCs). Target genes of HDAC10 were identified by RNA sequencing. We assessed the expression of dachshund homolog 1 (DACH1) and interferon regulatory factor 6 (IRF6) mRNA in ECSCs and normal endometrial stromal cells. The functions of DACH1 and IRF6 were confirmed by compulsory expression of these genes in ECSCs using lentivirus. Effects of tucidinostat and TH34 on the promoter acetylation of the DACH1 and IRF6 genes in ECSCs were assessed by chromatin immunoprecipitation assays. RESULTS: Both HDAC10Is had an inhibitory effect on the proliferation of ECSCs and caused them to enter cell cycle arrest at G0/G1. DACH1 and IRF6 were identified as the target genes of HDAC10. HDAC10Is caused acetylated histones to accumulate in the promoters of the genes encoding DACH1 and IRF6 in ECSCs. CONCLUSIONS: These findings indicate that HDAC10 is a factor which contributes to endometriosis pathogenesis by inhibiting DACH1 and IRF6 expression, and that HDAC10Is are therefore promising agents for endometriosis treatment.
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Methods

We assessed the effects of HDAC10Is, tucidinostat and TH34, on the proliferation and the cell cycle in human endometriotic cyst stromal cells (ECSCs). Target genes of HDAC10 were identified by RNA sequencing. We assessed the expression of dachshund homolog 1 (DACH1) and interferon regulatory factor 6 (IRF6) mRNA in ECSCs and normal endometrial stromal cells. The functions of DACH1 and IRF6 were confirmed by compulsory expression of these genes in ECSCs using lentivirus. Effects of tucidinostat and TH34 on the promoter acetylation of the DACH1 and IRF6 genes in ECSCs were assessed by chromatin immunoprecipitation assays.

Results

Both HDAC10Is had an inhibitory effect on the proliferation of ECSCs and caused them to enter cell cycle arrest at G0/G1. DACH1 and IRF6 were identified as the target genes of HDAC10. HDAC10Is caused acetylated histones to accumulate in the promoters of the genes encoding DACH1 and IRF6 in ECSCs.

Conclusions

These findings indicate that HDAC10 is a factor which contributes to endometriosis pathogenesis by inhibiting DACH1 and IRF6 expression, and that HDAC10Is are therefore promising agents for endometriosis treatment. Disclosure An earlier version of this article was presented at the Annual Meeting of Japan Endometriosis Society, which was held in Tokyo, Japan, on 20–21 January 2024, the Annual Meeting of Japan Society of Obstetrics and Gynecology, which was held in Kanagawa, Japan, on 19–21 April 2024, the Annual Meeting of Japan Endometriosis Society, which was held in Shiga, Japan, on 25–26 January 2025, and the 16th World Congress on Endometriosis 2025, which was held in Sidney, Australia, on 21–24 May 2025. Conflicts of Interest The authors declare no conflicts of interest. Data Availability Statement RNA sequencing data are available at Gene Expression Omnibus via the National Center for Biotechnology Information under Accession No. GSE309027 (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE309027).

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endometriosis

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Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis

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