Catalase Deficiency Compromises Survival in Extracellular Matrix-Detached SKOV3 Ovarian Cancer Cells

  • Cassandra L. Libbing Department of Biology, Saint Mary’s College, Notre Dame, IN 46556, USA
  • Kassidy M. Jungles Department of Biology, Saint Mary’s College, Notre Dame, IN 46556, USA
  • Ellen Rabaut Department of Biology, Saint Mary’s College, Notre Dame, IN 46556, USA
  • Calli A. Davison-Versagli Department of Biology, Saint Mary’s College, Notre Dame, IN 46556, USA
Keywords: Catalase; Extracellular matrix detachment; Metastasis; Ovarian cancer; SKOV3 ovarian cancer cell

Abstract

For epithelial ovarian cancer cells to survive during the metastatic cascade, cells must be able to evade anoikis, a caspase-dependent cell death mechanism initiated by extracellular matrix (ECM) detachment. However, many of the details behind this phenomenon have yet to be unveiled. Here, we examined the role of the antioxidant enzyme, catalase, in the survival and proliferation of anchorage-independent SKOV3 ovarian cancer cells. Catalase deficiency severely compromises cell viability and anchorage-independent growth in ECM-detached SKOV3 cells. Notably, cellviability and proliferation were unaffected in ECM-attached catalase-deficient SKOV3 cells. In aggregate, we discovered that catalase plays a prominent role in protection from ECM-detachment-induced cell death in SKOV3 cells. Furthermore, these findings imply that catalase may be an effective therapeutic target for epithelial ovarian cancer cells that survive the ECM-bereft metastatic cascade.

Published
2019-03-01
How to Cite
Libbing, C., Jungles, K., Rabaut, E., & Davison-Versagli, C. (2019). Catalase Deficiency Compromises Survival in Extracellular Matrix-Detached SKOV3 Ovarian Cancer Cells. Reactive Oxygen Species, 7(20), 121–128. Retrieved from https://www.aimsci.com/ros/index.php/ros/article/view/196
Section
Original Research Articles