Oncotarget

Research Papers:

Verrucarin J inhibits ovarian cancer and targets cancer stem cells

Kelsey Carter, Pranela Rameshwar, Mariusz Z. Ratajczak and Sham S. Kakar _

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Oncotarget. 2017; 8:92743-92756. https://doi.org/10.18632/oncotarget.21574

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Abstract

Kelsey Carter1, Pranela Rameshwar2, Mariusz Z. Ratajczak2,3,4 and Sham S. Kakar1,3

1Department of Physiology, University of Louisville, Louisville, KY, USA

2Department of Medicine, Hematology/Oncology, Rutgers, New Jersey Medical School, Newark, NJ, USA

3James Graham Brown Cancer Center, University of Louisville, Louisville, KY, USA

4Department of Medicine, University of Louisville, Louisville, KY, USA

Correspondence to:

Sham S. Kakar, email: [email protected]

Keywords: Verrucarin J, ovarian cancer, cancer stem cells, securin, tumor recurrence

Received: June 14, 2017     Accepted: September 08, 2017     Published: October 06, 2017

ABSTRACT

Ovarian Cancer is the fifth leading cause of death among women from cancer. Cancer stem cells are a small population of cells present in cancer and the cause of chemoresistance and recurrence of cancer. We tested a new compound “Verrucarin J (VJ)”, a metabolite of the Myrothecium fungus family, and showed that VJ significantly inhibits cell proliferation of both cisplatin-sensitive (A2780 and OVCAR5) and cisplatin-resistant (A2780/CP70) cell lines in a dose- and time-dependent manner with IC50 value of approximately 10 nM after 48 h of treatment. VJ was found to induce apoptosis, DNA damage, and generation of reactive oxygen species (ROS). Treatment of A2780 cells with VJ resulted in a significant suppression of expression of CSCs markers including ALDH1, LGR5, NANOG and OCT4 in a dose-dependent manner, elimination of ALDH1+ CSC population and inhibition of expression of Notch1 and Wnt1 signaling pathways. Our study also showed that VJ inhibited the tumorigenic potential (spheroid formation on ultralow attachment plates) of isolated ALDH1+ CSCs in vitro and tumor growth and metastasis in vivo. VJ resulted downregulation of expression of securin an “oncogene” involved in tumor growth and progression, indicating that securin may serve as a downstream signaling gene to mediate antitumor effects of VJ.


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