The Inherited Genetic Component of Sporadic Pancreatic Adenocarcinoma

Abstract

Pancreatic cancer, like many other complex diseases, has genetic and environmental components to its etiology. It is likely that relatively common genetic variants with modest effects on pancreatic cancer risk play an important role in both familial and sporadic forms of the disease, either individually or in interaction with environmental factors. The relatively highfrequencyofsuch variants meansthattheycould potentially explain a substantial portion of disease risk. Here we summarize the findings published to date from genetic association studies1. In general, very few low-penetrance variants have been identified and those that have require replication in independent studies. Possible gene-environment interactions arising from these studies also require replication. More comprehensive approaches are needed to make progress, including global analyses of biologically sound pathways and genome-wide association studies. Large samplesizesare required to do thisappropriatelyand multi-study consortia make this possible. A number of consortia of preexisting studies have already been formed, and these will facilitate the identification of further low-penetrance variants and gene-environment interaction. However, these approaches do not substitute for the design of novel, sufficiently powered studies that apply uniform criteria to case selection, the acquisition of environmental exposure information, and to biological sample collection.