A synthetic-lethality RNAi screen reveals an ERK-mTOR co-targeting pro-apoptotic switch in PIK3CA+ oral cancers

Oncotarget
Kosuke YamaguchiJ Silvio Gutkind

Abstract

mTOR inhibition has emerged as a promising strategy for head and neck squamous cell carcinomas (HNSCC) treatment. However, most targeted therapies ultimately develop resistance due to the activation of adaptive survival signaling mechanisms limiting the activity of targeted agents. Thus, co-targeting key adaptive mechanisms may enable more effective cancer cell killing. Here, we performed a synthetic lethality screen using shRNA libraries to identify druggable candidates for combinatorial signal inhibition. We found that the ERK pathway was the most highly represented. Combination of rapamycin with trametinib, a MEK1/2 inhibitor, demonstrated strong synergism in HNSCC-derived cells in vitro and in vivo, including HNSCC cells expressing the HRAS and PIK3CA oncogenes. Interestingly, cleaved caspase-3 was potently induced by the combination therapy in PIK3CA+ cells in vitro and tumor xenografts. Moreover, ectopic expression of PIK3CA mutations into PIK3CA- HNSCC cells sensitized them to the pro-apoptotic activity of the combination therapy. These findings indicate that co-targeting the mTOR/ERK pathways may provide a suitable precision strategy for HNSCC treatment. Moreover, PIK3CA+ HNSCC are particularly prone to undergo apoptosi...Continue Reading

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Citations

Mar 13, 2019·Molecular Systems Biology·Avinash Das SahuEytan Ruppin
Aug 20, 2017·Cancer Metastasis Reviews·Zhiyong WangJ Silvio Gutkind
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Nov 14, 2018·Clinical Cancer Research : an Official Journal of the American Association for Cancer Research·Terry A DayJ Silvio Gutkind

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Methods Mentioned

BETA
transfection
gene knockdown
xenograft
Protein Assay
electrophoresis

Software Mentioned

ToppGene Suite
GraphPad Prism
CompuSyn
GraphPad

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