Deoxycytidine Release from Pancreatic Stellate Cells Promotes Gemcitabine Resistance.
Ontology highlight
ABSTRACT: Pancreatic ductal adenocarcinoma (PDAC) is a leading cause of cancer deaths in the United States. The deoxynucleoside analogue gemcitabine is among the most effective therapies to treat PDAC, however, nearly all patients treated with gemcitabine either fail to respond or rapidly develop resistance. One hallmark of PDAC is a striking accumulation of stromal tissue surrounding the tumor, and this accumulation of stroma can contribute to therapy resistance. To better understand how stroma limits response to therapy, we investigated cell-extrinsic mechanisms of resistance to gemcitabine. Conditioned media from pancreatic stellate cells (PSC), as well as from other fibroblasts, protected PDAC cells from gemcitabine toxicity. The protective effect of PSC-conditioned media was mediated by secreti
SUBMITTER: Dalin S
PROVIDER: S-EPMC7357734 | biostudies-literature | 2019 Nov
REPOSITORIES: biostudies-literature
ACCESS DATA