A strategy to combine pathway-targeted low toxicity drugs in ovarian cancer

  • Delaney J
  • Patel C
  • McCabe K
  • et al.
Citations of this article
Mendeley users who have this article in their library.


Serous Ovarian Cancers (SOC) are frequently resistant to programmed cell death. However, here we describe that these programmed death-resistant cells are nonetheless sensitive to agents that modulate autophagy. Cytotoxicity is not dependent upon apoptosis, necroptosis, or autophagy resolution. A screen of NCBI yielded more than one dozen FDA-approved agents displaying perturbed autophagy in ovarian cancer. The effects were maximized via combinatorial use of the agents that impinged upon distinct points of autophagy regulation. Autophagosome formation correlated with efficacy in vitro and the most cytotoxic two agents gave similar effects to a pentadrug combination that impinged upon five distinct modulators of autophagy. However, in a complex in vivo SOC system, the pentadrug combination outperformed the best two, leaving trace or no disease and with no evidence of systemic toxicity. Targeting the autophagy pathway in a multi-modal fashion might therefore offer a clinical option for treating recalcitrant SOC.




Delaney, J. R., Patel, C., McCabe, K. E., Lu, D., Davis, M.-A., Tancioni, I., … Stupack, D. G. (2015). A strategy to combine pathway-targeted low toxicity drugs in ovarian cancer. Oncotarget, 6(31). https://doi.org/10.18632/oncotarget.5093

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free