# A Novel HDAC6 Inhibitor Enhances the Efficacy of Paclitaxel Against Ovarian Cancer Cells

**Authors:** An-Jui Chi, Jui-Ling Hsu, Yun-Xin Xiao, Ji-Wang Chern, Jih-Hwa Guh, Chao-Wu Yu, Lih-Ching Hsu

PMC · DOI: 10.3390/molecules30132793 · 2025-06-28

## TL;DR

A new HDAC6 inhibitor, when combined with paclitaxel, shows strong anti-cancer effects in ovarian cancer cells by inducing apoptosis and reducing cell growth.

## Contribution

Compound 25253 is a novel HDAC6 inhibitor that synergizes with paclitaxel to enhance its anti-ovarian cancer effects.

## Key findings

- Compound 25253 and paclitaxel combination significantly induced apoptosis in ovarian cancer cells.
- The combination increased DNA damage markers and inhibited cell migration and invasion.
- HDAC6 inhibition led to increased acetylated α-tubulin, affecting microtubule dynamics.

## Abstract

Ovarian cancer cells overexpress HDAC6, and selective HDAC6 inhibitors have been considered potential new drugs for ovarian cancer either alone or in combination with other anticancer agents. We screened 46 potential novel HDAC6 inhibitors in ES-2 ovarian cancer cells and showed that compound 25253 demonstrated the most potent anti-proliferative activity and effective synergy with paclitaxel, which was also validated in TOV21G ovarian cancer cells. The combination of 25253 and paclitaxel significantly induced subG1 and apoptotic cells, revealed by PI staining assay and Annexin V-FITC/PI double staining assay, respectively. Western blot analysis showed downregulation of Bcl-2 and Bcl-XL, and upregulation of Bax and Bak, indicating that apoptosis was mediated through the intrinsic pathway. The combination increased γ-H2AX and p-p53 protein levels, suggesting the induction of DNA damage. Furthermore, HDAC6 was downregulated and acetylated α-tubulin was profoundly increased. Compound 25253 enhanced the inhibitory effect of paclitaxel on cell migration and invasion, possibly due to the extensive accumulation of acetylated α-tubulin, which affected microtubule dynamics. Taken together, the combination of 25253 and paclitaxel synergistically inhibited the growth, migration, and invasion of ovarian cancer cells and induced apoptosis, providing supporting evidence that the combination of HDAC6 inhibitors and paclitaxel may be a promising treatment strategy for ovarian cancer.

## Linked entities

- **Genes:** BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596], Bcl2l1 (BCL2-like 1) [NCBI Gene 12048], BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581], BAK1 (BCL2 antagonist/killer 1) [NCBI Gene 578], TP53 (tumor protein p53) [NCBI Gene 7157]
- **Proteins:** HDAC6 (histone deacetylase 6), H2AXA (Histone superfamily protein), H3V24_gp67 (terminase small subunit)
- **Chemicals:** paclitaxel (PubChem CID 36314)
- **Diseases:** ovarian cancer (MONDO:0005140)

## Full-text entities

- **Genes:** BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}, BAK1 (BCL2 antagonist/killer 1) [NCBI Gene 578] {aka BAK, BAK-LIKE, BCL2L7, CDN1}, BCL2L1 (BCL2 like 1) [NCBI Gene 598] {aka BCL-XL/S, BCL2L, BCLX, Bcl-X, PPP1R52}, HDAC6 (histone deacetylase 6) [NCBI Gene 10013] {aka CPBHM, HD6, JM21, KDAC6, PPP1R90}, TUBA1B (tubulin alpha 1b) [NCBI Gene 10376] {aka K-ALPHA-1}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}
- **Diseases:** Ovarian Cancer (MESH:D010051)
- **Chemicals:** Compound 25253 (-), PI (MESH:D010716), Paclitaxel (MESH:D017239)
- **Cell lines:** TOV21G — Homo sapiens (Human), Ovarian clear cell adenocarcinoma, Cancer cell line (CVCL_3613), ES-2 — Homo sapiens (Human), Embryonic stem cell (CVCL_C769)

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12251222/full.md

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Source: https://tomesphere.com/paper/PMC12251222