| Literature DB >> 24518495 |
Chang Moo Kang1, Michele L Babicky, Andrew M Lowy.
Abstract
Pancreatic cancer remains a devastating disease with a mortality rate that has not changed substantially in decades. Novel therapies are therefore desperately needed. The RON receptor tyrosine kinase has been identified as an important mediator of KRAS oncogene addiction and is overexpressed in the majority of pancreatic cancers. Preclinical studies show that inhibition of RON function decreases pancreatic cancer cell migration, invasion, and survival and can sensitize pancreatic cancer cells to chemotherapy. This article reviews the current state of knowledge regarding RON biology and pancreatic cancer and discusses its potential as a therapeutic target.Entities:
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Year: 2014 PMID: 24518495 PMCID: PMC4009395 DOI: 10.1097/MPA.0000000000000088
Source DB: PubMed Journal: Pancreas ISSN: 0885-3177 Impact factor: 3.327