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- W3137173150 endingPage "533" @default.
- W3137173150 startingPage "525" @default.
- W3137173150 abstract "Pancreatic ductal adenocarcinoma (PDAC), the most common histological subtype of pancreatic cancer, has one of the highest case fatality rates of all known solid malignancies. Over the past decade, several landmark studies have established mutations in KRAS and TP53 as the predominant drivers of PDAC pathogenesis and therapeutic resistance, though treatment options for PDACs and other tumors with these mutations remain extremely limited. Hampered by late tumor discovery and diagnosis, clinicians are often faced with using aggressive and non-specific chemotherapies to treat advanced disease. Clinically meaningful responses to targeted therapy are often limited to the minority of patients with susceptible PDACs, and immunotherapies have routinely encountered roadblocks in effective activation of tumor-infiltrating immune cells. Alternative RNA splicing (ARS) has recently gained traction in the PDAC literature as a field from which we may better understand and treat complex mechanisms of PDAC initiation, progression, and therapeutic resistance. Here, we review PDAC pathogenesis as it relates to fundamental ARS biology, with an extension to implications for PDAC patient clinical management." @default.
- W3137173150 created "2021-03-29" @default.
- W3137173150 creator A5028680767 @default.
- W3137173150 creator A5051759283 @default.
- W3137173150 creator A5079259494 @default.
- W3137173150 date "2021-03-16" @default.
- W3137173150 modified "2023-09-26" @default.
- W3137173150 title "Pancreatic cancer driver mutations are targetable through distant alternative RNA splicing dependencies" @default.
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