HSP90 inhibition potentiates oxidant-based antimelanoma action of novel thioquercetin derivatives by compromising AhR/CYP1A1 pathway
Quercetin, a plant-derived dietary flavonoid, has multifunctional biological activities, including anticancer action; however, its applications may be restricted due to limited bioavailability. Thus, novel synthetic quercetin derivatives (QDs) with improved properties and/or drug combinations should be designed and tested. In the present study, anticancer activity of fourteen newly synthesized QDs was investigated using four cellular models of melanoma, namely A375, MM370, G-361, and SH-4 cells. Thioquercetins (thioQ, thioQ(OAc)<sub>4</sub>, and thioQ(OAc)<sub>5</sub>), when used at low micromolar range, induced apoptotic cell death in melanoma cells compared to normal cells. Thioquercetins also reduced the population of spheroid-forming cells and suppressed the growth of A375 cells in 3D spheroid models. Thioquercetin-mediated antimelanoma action was potentiated upon heat shock protein 90 (HSP90) inhibition. Co-treatment with the HSP90 inhibitor 17-DMAG and thioquercetins augmented oxidative stress (increased superoxide production, decreased levels of antioxidant proteins SOD1, and PRDX1-2), and impaired the aryl hydrocarbon receptor (AhR)/cytochrome P450 1A1 (CYP1A1) signaling pathway-based detoxification of thioquercetins by the inhibition of AhR translocation to the nucleus and AhR-mediated stimulation of CYP1A1 expression leading to enhanced cytotoxic effects against melanoma cells. The senolytic activity of thioQ(OAc)<sub>4</sub> with four acetylated hydroxy groups against cisplatin-induced senescent melanoma cells was also revealed in selected experimental settings. We suggest that the use of novel thioquercetin-based derivatives along with HSP90 inhibitors should be further validated in vivo and considered for the design of more effective antimelanoma strategies in the future.
Authors
- Anna Lewińska (ORCID: https://orcid.org/0000-0001-8055-1918)
- Maciej Wnuk (ORCID: https://orcid.org/0000-0002-8518-6670)
- Pawel Zayakin (ORCID: https://orcid.org/0000-0002-5336-3484)
- Grzegorz Litwinienko (ORCID: https://orcid.org/0000-0002-5523-0888)
- María Moros (ORCID: https://orcid.org/0000-0002-2861-2469)
- Anna Deręgowska (ORCID: https://orcid.org/0000-0001-5354-3365)
- Michał Żebrowski (ORCID: https://orcid.org/0009-0003-6781-165X)
- Wojciech Witkowski (ORCID: https://orcid.org/0000-0001-8873-9819)
- P. Piotrowski
- Julia Słaby (ORCID: https://orcid.org/0009-0002-1906-076X)
- Paulina Stec
- Nadezhda Romanchikova
- Martyna Cybularczyk-Cecotka
- Aija Linē
Institutions
- Latvia University of Life Sciences and Technologies (LV)
- Latvian Biomedical Research and Study Centre (LV)
- Universidad de Zaragoza (ES)
- Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine (ES)
- Instituto de Nanociencia y Materiales de Aragón (ES)
- University of Warsaw (PL)
- University of Latvia (LV)
- University of Rzeszów (PL)
Publication Details
- Journal
- APOPTOSIS
- Published
- 2026-03-28
- DOI
- https://doi.org/10.1007/s10495-026-02311-4
- Primary Topic
- Heat shock proteins research
- Type
- article
- Field-Weighted Citation Impact
- 0.00