ABT-898 induces tumor regression and prolongs survival in a mouse model of epithelial ovarian cancer

Nicole Campbell, James Greenaway, Jack Henkin, Jim Petrik*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

35 Scopus citations


Epithelial ovarian cancer (EOC) is the most lethal gynecologic malignancy and is often not diagnosed until late stages due to its asymptomatic nature. Women diagnosed with EOC typically undergo surgical debulking followed by chemotherapy; however, disease recurrence often occurs. In this study, we evaluated the ability of the thrombospondin-1 mimetic peptide, ABT-898, to regress established, late-stage tumors in a mouse model of human EOC. Ovarian tumors were induced and ABT-898 treatment was initiated at time points that were representative of late stages of the disease to study tumor regression. ABT-898 induced tumor regression and reduced the morbidity of treated animals compared with controls. Analysis of tumors from ABT-898-treated animals showed reduced abnormal tumor vasculature, decreased expression of the proangiogenic compound VEGF, and reduced tumor tissue hypoxia. ABT-898 treatment initiated at late-stage disease also significantly prolonged disease-free survival compared with control animals. Results from this study show that ABT-898 is capable of regressing established ovarian tumors in an animal model of the disease. As most women are detected at advanced stage EOC, ABT-898 may improve our treatment of ovarian cancer.

Original languageEnglish (US)
Pages (from-to)1876-1885
Number of pages10
JournalMolecular cancer therapeutics
Issue number10
StatePublished - Oct 2011

ASJC Scopus subject areas

  • Oncology
  • Cancer Research


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