| Literature DB >> 31262852 |
Daniel Ansari1, Henrik Ohlsson1, Carl Althini1, Monika Bauden1, Qimin Zhou1,2, Dingyuan Hu1,3, Roland Andersson4.
Abstract
Hippo signaling is a key regulator of organ size, tissue hemostasis and regeneration. Dysregulation of the Hippo pathway has been recognized in a variety of human cancers, including pancreatic cancer. YES-associated protein (YAP) and transcriptional coactivator with PDZ-binding motif (TAZ) are the two major downstream effectors of the Hippo pathway. YAP and TAZ have been found to promote pancreatic tumor development and progression, even in the absence of mutant Kirsten RAS (KRAS). Pancreatic cancer is associated with an abundant stromal reaction leading to tumor growth and immune escape. It has been found that YAP and TAZ modulate behavior of pancreatic stellate cells and recruitment of tumor-associated macrophages and myeloid-derived suppressor cells. Moreover, YAP and TAZ are associated with chemoresistance and poor prognosis in pancreatic cancer. This review dissects the role of Hippo signaling in pancreatic cancer, focusing on molecular mechanisms and prospects for future intervention. CopyrightEntities:
Keywords: EMT; Hippo pathway; Pancreatic Cancer; TAZ; YAP; chemoresistance; immunomodulation; review; stroma; treatment; tumor progression
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Year: 2019 PMID: 31262852 DOI: 10.21873/anticanres.13474
Source DB: PubMed Journal: Anticancer Res ISSN: 0250-7005 Impact factor: 2.480