Targeting constitutively-activated STAT3 in hypoxic ovarian cancer, using a novel STAT3 inhibitor

Georgia A. McCann, Shan Naidu, Kellie S. Rath, Hemant K. Bid, Brent J. Tierney, Adrian Suarez, Saradhadevi Varadharaj, Jianying Zhang, Kálmán Hideg, Peter Houghton, Periannan Kuppusamy, David E. Cohn, Karuppaiyah Selvendiran

Research output: Contribution to journalArticle

24 Citations (Scopus)

Abstract

Tumor hypoxia, a feature of many solid tumors including ovarian cancer, is associated with resistance to therapies. We previously demonstrated that hypoxic exposure results in increased expression of phosphorylated signal transducer and activator of transcription 3 (pSTAT3). We hypothesized the activation of STAT3 could lead to chemotherapeutic resistance in ovarian cancer cells in hypoxic conditions. In this study, we demonstrate the level of pSTAT3 Tyr705 is increased in the hypoxic regions of human epithelial ovarian cancer (EOC) specimens, as determined by HIF- 1a and CD-31 staining. In vitro mutagenesis studies proved that pSTAT3 Tyr705 is necessary for cell survival and proliferation under hypoxic conditions. In addition, we show that S1PR1, a regulator of STAT3 transcription via the JAK/STAT pathway, is highly expressed in hypoxic ovarian cancer cells (HOCCs). Knock down of S1PR1 in HOCCs reduced pSTAT3 Tyr705 levels and was associated with decreased cell survival. Treatment of HOCCs with the STAT3 inhibitor HO-3867 resulted in a rapid and dramatic decrease in pSTAT3 Tyr705 levels as a result of ubiquitin proteasome degradation. STAT3-target proteins Bcl-xL, cyclin D2 and VEGF showed similar decreases in HO- 3867 treated cells. Taken together, these findings suggest that activation of STAT3 Tyr705 promotes cell survival and proliferation in HOCCs, and that S1PR1 is involved in the initiation of STAT3 activation. Targeting hypoxia-mediated STAT3 activation represents a therapeutic option for ovarian cancer and other solid tumors.

Original languageEnglish
Pages (from-to)216-228
Number of pages13
JournalOncoscience
Volume1
Issue number3
DOIs
Publication statusPublished - 2014

Keywords

  • Chemo-resistance
  • HO-3867
  • Hypoxia
  • Ovarian cancer
  • STAT3

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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    McCann, G. A., Naidu, S., Rath, K. S., Bid, H. K., Tierney, B. J., Suarez, A., Varadharaj, S., Zhang, J., Hideg, K., Houghton, P., Kuppusamy, P., Cohn, D. E., & Selvendiran, K. (2014). Targeting constitutively-activated STAT3 in hypoxic ovarian cancer, using a novel STAT3 inhibitor. Oncoscience, 1(3), 216-228. https://doi.org/10.18632/oncoscience.26