Oncogenic KRAS engages multiple effector pathways including the MAPK cascade to promote proliferation and survival of pancreatic cancer cells. KRAS-transformed cancer cells exhibit oncogene addiction to sustained activity of RAS for maintenance of malignant phenotypes. Previously, we have shown an essential role for the RHO guanine exchange factor ARHGEF2 for growth and survival of RAS-transformed pancreatic tumors. Here, we have determined that pancreatic cancer cells demonstrating KRAS addiction are significantly dependent on expression of . Furthermore, enforced expression of ARHGEF2 desensitizes cells to pharmacological MEK inhibition and initiates a positive feedback loop which activates ERK phosphorylation and the downstream promoter. Therefore, targeting expression may increase the efficacy of MAPK inhibitors for treatment of RAS-dependent pancreatic cancers.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6748365 | PMC |
| http://dx.doi.org/10.1080/21541248.2017.1337545 | DOI Listing |
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