Transcription Factor 7-Like 2 Regulates β-Cell Survival and Function in Human Pancreatic Islets
Author(s) -
Luan Shu,
Nadine S. Sauter,
Fabienne T. Schulthess,
Aleksey V. Matveyenko,
José Oberholzer,
Kathrin Maedler
Publication year - 2007
Publication title -
diabetes
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.219
H-Index - 330
eISSN - 1939-327X
pISSN - 0012-1797
DOI - 10.2337/db07-0847
Subject(s) - tcf7l2 , biology , apoptosis , pancreatic islets , beta cell , endocrinology , small interfering rna , medicine , transcription factor , cancer research , islet , microbiology and biotechnology , insulin , cell culture , gene , biochemistry , transfection , genetics , genotype , single nucleotide polymorphism
Type 2 diabetes is characterized by impaired insulin secretion in response to increased metabolic demand. This defect in beta-cell compensation seems to result from the interplay between environmental factors and genetic predisposition. Genome-wide association studies reveal that common variants in transcription factor 7-like 2 (TCF7L2) are associated with increased risk of type 2 diabetes. The aim of the present study was to establish whether TCF7L2 plays a role in beta-cell function and/or survival.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom