High-effect synergy from dual HDAC6 and YAP–TEAD inhibition in ovarian clear cell carcinoma

Ovarian clear cell carcinoma (OCCC) is an aggressive epithelial subtype characterized by intrinsic chemoresistance and limited targeted therapies. Transcriptional programs driven by Yes-associated protein (YAP) and TEA domain (TEAD) factors support tumor stress adaptation, suggesting that this axis represents therapeutic vulnerability. Histone deacetylase 6 (HDAC6) has been linked to Hippo/YAP regulation. We hypothesized that dual inhibition of HDAC6 and YAP-TEAD would converge on the YAP axis and yield synergistic cytotoxicity in OCCC. We first analyzed a tissue microarray (TMA) of 171 OCCC cases stained for HDAC6, YAP, and connective tissue growth factor (CTGF) to assess correlations and survival associations. Guided by these findings, we treated HAC2, OVTOKO, and RMG-1 cells with fixed-ratio combinations of the HDAC6 inhibitor citarinostat and the YAP-TEAD disruptor verteporfin (VP). Drug interactions were quantified using Loewe isobolograms and the Chou-Talalay combination index (CI). Immunofluorescence was used to measure total YAP (t-YAP) and the nuclear-cytoplasmic (N/C) ratio, while RT-qPCR assessed YAP, CTGF, and CYR61 transcripts. In HAC2, western blotting analysis was performed for the expression of CTGF protein. The selected assays were reproduced with the distinct YAP-TEAD inhibitor CA-3. In patient tissues, cytoplasmic HDAC6 correlated positively with cytoplasmic YAP and CTGF, and inversely with nuclear HDAC6, but none of the markers predicted survival. Across all three cell lines, dual treatment produced robust, high-effect synergy (minimum CI ≈ 0.08–0.28). In HAC2, the combination increased t-YAP but reduced the N/C ratio, indicating restricted nuclear access. VP alone decreased t-YAP, whereas synergy was confirmed with CA-3, suggesting that TEAD disruption is the relevant mechanism. RT-qPCR revealed divergent cell line-specific transcriptional responses, with CTGF and CYR61 often upregulated by citarinostat and suppressed by VP or combination. The CTGF-HDAC6 correlation in the TMA supports the biological relevance of this axis, whereas early transcript changes likely reflect compensatory feedback. An investigation from the clinic to bench identified an HDAC6-YAP-CTGF axis in OCCC and demonstrated that dual HDAC6 and YAP-TEAD inhibition yields strong high-effect synergy by restricting YAP nuclear access and limiting TEAD engagement. These findings may provide a rationale for biomarker-guided validation of citarinostat-VP combinations in organoids, in vivo models, and early-phase clinical studies.

Authors

Institutions

Publication Details

Journal
Cancer Cell International
Published
2026-01-30
DOI
https://doi.org/10.1186/s12935-026-04204-7
Primary Topic
Hippo pathway signaling and YAP/TAZ
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

High-effect synergy from dual HDAC6 and YAP–TEAD inhibition in ovarian clear cell carcinoma

Keiko Matsuura, Eiji Kobayashi, Sumika Zaitsu, Masanori Yasuda et al.
Cancer Cell International
Hippo pathway signaling and YAP/TAZ
article

High-effect synergy from dual HDAC6 and YAP–TEAD inhibition in ovarian clear cell carcinoma

Keiko Matsuura, Eiji Kobayashi, Sumika Zaitsu, Masanori Yasuda, Sohei Sakashita, Maiko Miwa, Mitsutake Yano
article en

Abstract

Ovarian clear cell carcinoma (OCCC) is an aggressive epithelial subtype characterized by intrinsic chemoresistance and limited targeted therapies. Transcriptional programs driven by Yes-associated protein (YAP) and TEA domain (TEAD) factors support tumor stress adaptation, suggesting that this axis represents therapeutic vulnerability. Histone deacetylase 6 (HDAC6) has been linked to Hippo/YAP regulation. We hypothesized that dual inhibition of HDAC6 and YAP-TEAD would converge on the YAP axis and yield synergistic cytotoxicity in OCCC. We first analyzed a tissue microarray (TMA) of 171 OCCC cases stained for HDAC6, YAP, and connective tissue growth factor (CTGF) to assess correlations and survival associations. Guided by these findings, we treated HAC2, OVTOKO, and RMG-1 cells with fixed-ratio combinations of the HDAC6 inhibitor citarinostat and the YAP-TEAD disruptor verteporfin (VP). Drug interactions were quantified using Loewe isobolograms and the Chou-Talalay combination index (CI). Immunofluorescence was used to measure total YAP (t-YAP) and the nuclear-cytoplasmic (N/C) ratio, while RT-qPCR assessed YAP, CTGF, and CYR61 transcripts. In HAC2, western blotting analysis was performed for the expression of CTGF protein. The selected assays were reproduced with the distinct YAP-TEAD inhibitor CA-3. In patient tissues, cytoplasmic HDAC6 correlated positively with cytoplasmic YAP and CTGF, and inversely with nuclear HDAC6, but none of the markers predicted survival. Across all three cell lines, dual treatment produced robust, high-effect synergy (minimum CI ≈ 0.08–0.28). In HAC2, the combination increased t-YAP but reduced the N/C ratio, indicating restricted nuclear access. VP alone decreased t-YAP, whereas synergy was confirmed with CA-3, suggesting that TEAD disruption is the relevant mechanism. RT-qPCR revealed divergent cell line-specific transcriptional responses, with CTGF and CYR61 often upregulated by citarinostat and suppressed by VP or combination. The CTGF-HDAC6 correlation in the TMA supports the biological relevance of this axis, whereas early transcript changes likely reflect compensatory feedback. An investigation from the clinic to bench identified an HDAC6-YAP-CTGF axis in OCCC and demonstrated that dual HDAC6 and YAP-TEAD inhibition yields strong high-effect synergy by restricting YAP nuclear access and limiting TEAD engagement. These findings may provide a rationale for biomarker-guided validation of citarinostat-VP combinations in organoids, in vivo models, and early-phase clinical studies.

Cancer Cell InternationalVol. 26(1)
Oita University (JP), Saitama Medical University (JP)
Good health and well-being
Openalex Percentile: Top 74%
Hippo pathway signaling and YAP/TAZ
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.