Abstract
Pancreatic cancer is increasing in incidence and is expected to be the second leading cause of cancer-related mortality by the year 2030. Understanding molecular pathways that contribute to pancreatic cancer initiation and progression provides the opportunity to uncover potential molecular vulnerabilities that can be exploited therapeutically. In this issue of Cancer Research, Lee and colleagues provide compelling evidence that BRCA1-associated protein (BAP1) functions as a tumor suppressor in pancreatic cancer by promoting the activity of the Hippo tumor suppressor pathway, highlighting YAP and TAZ, Hippo effectors, as attractive therapeutic targets in pancreatic ductal adenocarcinoma, especially in BAP1-deficient or low tumors.See related article by Lee et al., p. 1656.
Sign-in/Register to access full text options 
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
