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Valproic Acid as a Promising Co-Treatment With Paclitaxel and Doxorubicin in Different Ovarian Carcinoma Cell Lines
  1. Patrycja Kwiecińska, PhD,
  2. Erik Taubøll, PhD,
  3. Edyta Grzyb, MSc,
  4. Elżbieta Fiedor, MSc,
  5. Anna Ptak, PhD and
  6. Ewa Lucja Gregoraszczuk, PhD
  1. * Department of Physiology and Toxicology of Reproduction, Institute of Zoology, Jagiellonian University, Kraków, Poland; and
  2. Division of Surgery and Clinical Neurosciences, Department of Neurology, Oslo University Hospital-Rikshospitalet; and
  3. University of Oslo, Oslo, Norway.
  1. Address correspondence and reprint requests to Ewa Lucja Gregoraszczuk, Department of Physiology and Toxicology of Reproduction, Institute of Zoology, Jagiellonian University, Gronostajowa 9, 30-387 Kraków, Poland. E-mail: ewa.gregoraszczuk{at}


Objective The current preferred treatment of ovarian cancer is combination chemotherapy, usually a platinum-based drug coupled with paclitaxel (PTX). Here, we investigated whether co-treatment with valproic acid (VPA) could increase the efficiency of various ovarian cancer drugs—PTX, doxorubicin (DOX), carboplatin (CBP), and cyclophosphamide (CP)—in different ovarian cancer cell lines.

Methods Three different ovarian cancer cell lines (OVCAR-3, TOV-21G, and TOV-112D) were treated with chemotherapeutic drugs, alone or in combination with VPA. Cell viability (XTT assay), caspase-3 activity, and the expression of cell cycle– and apoptosis-related genes and proteins were assessed. Furthermore, the effects of these drugs on α-tubulin acetylation and DNA fragmentation were investigated.

Results Paclitaxel and DOX decreased cell viability and increased caspase-3 activity, and co-treatment with VPA enhanced this effect. Carboplatin and CP had no effect. Responses to treatment with PAX and DOX together with VPA on gene expression profile were highly variable and depended on the cell line investigated. However, a common feature in all cell lines was an increased expression of CDKN1A, CCNE1, PARP1, and PARP3. Co-treatment with VPA enhanced the effect of DOX and PAX on most protein expressions investigated in TOV-21G and TOV-112D cell lines, whereas in OVCAR-3, the most effect was seen with DOX with VPA. Valproic acid did not increase PTX-induced α-tubulin acetylation. An additive effect of DOX with VPA on DNA fragmentation was observed in TOV-21G and TOV-112D cell lines but not in the OVCAR-3.

Conclusions Our results indicate that VPA could be a promising agent in combined anticancer therapy for ovarian cancer, with the combination of VPA and DOX being the most effective. Certainly, additional in vivo and ex vivo experiments are necessary to investigate the molecular mechanisms of action underlying the cellular effects reported here and to study possible clinically relevant effects in ovarian cancer explants.

  • Valproic acid
  • Paclitaxel
  • Doxorubicin
  • Epithelial ovarian cancer cell lines

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  • The authors declare no conflicts of interest.