Tumor necrosis factor-α related gene response to Epothilone B in ovarian cancer

Dineo Khabele, Melissa Lopez-Jones, Wan Cai Yang, Diego Arango, Susan J. Gross, Leonard H. Augenlicht, Gary L. Goldberg

Research output: Contribution to journalArticlepeer-review

11 Scopus citations


Objectives. Epothilone B (EpoB) is a non-taxane microtubule-stabilizing agent with a mode of action similar to that of paclitaxel, but with the advantage of being active in paclitaxel-resistant cells. Knowledge regarding other mechanisms of EpoB action is limited. The purpose of this study was to identify gene expression profiles associated with the biological response to EpoB in an ovarian cancer cell line (SKOV3). Methods. SKOV3 cells were maintained in McCoy's 5A media. Equal densities cells were treated with or without EpoB, and were evaluated for cell growth arrest and apoptosis. mRNA expression was evaluated by cDNA microarrays and quantitative, real time reverse transcription polymerase chain reaction (QRTPCR). Results. EpoB (10 nM) led to cell cycle arrest and apoptosis in SKOV3 cells. Microarray analysis, comparing EpoB-treated to untreated cells, revealed altered expression of 41 genes. There was a predominance of sequences related to the TNFα stress response pathway. Differential expression of selected genes was confirmed by QRTPCR. Conclusions. We demonstrated that cDNA microarrays are a useful tool to rapidly screen for patterns of gene expression that characterize drug response. The microarray data suggest that the microtubule-stabilizing agent, EpoB, triggers stress-related signal transduction pathways related to TNFα. These pathways may contribute to mechanisms of EpoB action and potential mechanisms of resistance in ovarian cancer.

Original languageEnglish (US)
Pages (from-to)19-26
Number of pages8
JournalGynecologic Oncology
Issue number1
StatePublished - Apr 2004


  • Epothilone B
  • Necrosis
  • Ovarian cancer

ASJC Scopus subject areas

  • Oncology
  • Obstetrics and Gynecology


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