Unknown

Dataset Information

0

Leveraging Mechanisms Governing Pancreatic Tumorigenesis To Reduce Pancreatic Cancer Mortality.


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.

SUBMITTER: Donahue TR 

PROVIDER: S-EPMC5075262 | biostudies-literature | 2016 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

Leveraging Mechanisms Governing Pancreatic Tumorigenesis To Reduce Pancreatic Cancer Mortality.

Donahue Timothy R TR   Dawson David W DW  

Trends in endocrinology and metabolism: TEM 20160725 11


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  ...[more]

Similar Datasets

| S-EPMC4864151 | biostudies-literature
| S-EPMC6365013 | biostudies-literature
| S-EPMC1931565 | biostudies-literature
| S-EPMC3576034 | biostudies-literature
2016-04-12 | GSE79469 | GEO
| S-EPMC4931723 | biostudies-literature
| S-EPMC1794698 | biostudies-other
| S-EPMC4896979 | biostudies-literature
| S-EPMC6692915 | biostudies-literature