| Literature DB >> 27461042 |
Timothy R Donahue1, David W Dawson2.
Abstract
Pancreatic ductal adenocarcinoma (PDA) is a devastating malignancy with limited and modest clinical treatments. High-throughput technologies and accurate disease models now provide a comprehensive picture of the diverse molecular signaling pathways and cellular processes governing PDA tumorigenesis. Central among these is oncogenic KRAS, a mediator of cellular plasticity, metabolic reprogramming, and inflammatory and paracrine signaling required for tumor development and maintenance. Biological aggressiveness is further conferred by a highly fibrotic and immunosuppressive PDA microenvironment that also acts as a barrier to effective drug delivery. The regulation of these mechanisms and their implications for early cancer detection, chemoprevention and therapy are discussed.Entities:
Keywords: KRAS; immunotherapy; pancreatic cancer; precision medicine; tumor–stroma interactions
Mesh:
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Year: 2016 PMID: 27461042 PMCID: PMC5075262 DOI: 10.1016/j.tem.2016.06.009
Source DB: PubMed Journal: Trends Endocrinol Metab ISSN: 1043-2760 Impact factor: 12.015