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Updated: May 23, 2026

A Murine Pancreatic Islet Cell-based Screening for Diabetogenic Environmental Chemicals
Published on: June 25, 2018
Role of forkhead transcription factors in diabetes-induced oxidative stress
Bhaskar Ponugoti1, Guangyu Dong, Dana T Graves
1School of Dental Medicine, University of Pennsylvania, Philadelphia, PA 19104-6030, USA.
Abstract:
Diabetes is a chronic metabolic disorder, characterized by hyperglycemia resulting from insulin deficiency and/or insulin resistance. Recent evidence suggests that high levels of reactive oxygen species (ROS) and subsequent oxidative stress are key contributors in the development of diabetic complications. The FOXO family of forkhead transcription factors including FOXO1, FOXO3, FOXO4, and FOXO6 play important roles in the regulation of many cellular and biological processes and are critical regulators of cellular oxidative stress response pathways. FOXO1 transcription factors can affect a number of different tissues including liver, retina, bone, and cell types ranging from hepatocytes to microvascular endothelial cells and pericytes to osteoblasts. They are induced by oxidative stress and contribute to ROS-induced cell damage and apoptosis. In this paper, we discuss the role of FOXO transcription factors in mediating oxidative stress-induced cellular response.
Insights
This study explores how FOXO transcription factors regulate cellular responses to oxidative stress, a key factor in diabetes complications. Understanding FOXO
Area of Science:
- Molecular Biology
- Cellular Biology
- Endocrinology
Background:
- Diabetes mellitus is a chronic metabolic disorder marked by hyperglycemia.
- Oxidative stress, driven by reactive oxygen species (ROS), significantly contributes to diabetic complications.
- FOXO transcription factors are crucial regulators of cellular oxidative stress response pathways.
Purpose of the Study:
- To elucidate the role of FOXO transcription factors in mediating cellular responses to oxidative stress.
- To highlight the involvement of FOXO factors in the pathogenesis of diabetic complications.
Main Methods:
- Literature review of studies investigating FOXO transcription factors and oxidative stress.
- Analysis of FOXO1's impact on various tissues and cell types relevant to diabetes.
- Discussion of FOXO-mediated pathways in response to ROS.
Main Results:
- FOXO transcription factors (FOXO1, FOXO3, FOXO4, FOXO6) are induced by oxidative stress.
- FOXO1 influences multiple tissues (liver, retina, bone) and cell types (hepatocytes, endothelial cells, pericytes, osteoblasts).
- FOXO factors contribute to ROS-induced cellular damage and apoptosis.
Conclusions:
- FOXO transcription factors play a critical role in the cellular response to oxidative stress.
- Targeting FOXO pathways may offer therapeutic strategies for mitigating diabetic complications.
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