- Integration of CiNii Books functions for fiscal year 2025 has completed
- Trial version of CiNii Research Knowledge Graph Search feature is available on CiNii Labs
- 【Updated on November 26, 2025】Regarding the recording of “Research Data” and “Evidence Data”
- Start the collection of all publicly IRDB content
- Incorporate Research Data from KAKEN
Emerging Targets for Therapeutic Development in Diabetes and Its Complications: The RAGE Signaling Pathway
-
- EMS Litwinoff
- Diabetes Research Program Division of Endocrinology Department of Medicine New York University School of Medicine New York New York USA
-
- C Hurtado del Pozo
- Diabetes Research Program Division of Endocrinology Department of Medicine New York University School of Medicine New York New York USA
-
- R Ramasamy
- Diabetes Research Program Division of Endocrinology Department of Medicine New York University School of Medicine New York New York USA
-
- AM Schmidt
- Diabetes Research Program Division of Endocrinology Department of Medicine New York University School of Medicine New York New York USA
Bibliographic Information
- Published
- 2015-06-25
- Rights Information
-
- http://onlinelibrary.wiley.com/termsAndConditions#vor
- DOI
-
- 10.1002/cpt.148
- Publisher
- Wiley
Search this article
Description
<jats:p>Types 1 and 2 diabetes are on the rise worldwide. Although the treatment of hyperglycemia has benefited from recent advances, aggressive efforts to maintain euglycemia may be fraught with risk, especially in older subjects or in subjects vulnerable to hypoglycemic unawareness. Hence, strategies to prevent and treat the complications of hyperglycemia are essential. In this review we summarize recent updates on the biology of the receptor for advanced glycation endproducts (RAGE) in the pathogenesis of both micro‐ and macrovascular complications of diabetes, insights from the study of mouse models of obesity and diabetic complications, and from associative studies in human subjects. The study of the mechanisms and consequences of the interaction of the RAGE cytoplasmic domain with the formin, mDia1, in RAGE signal transduction, will be discussed. Lastly, we review the "state‐of‐the‐art" on RAGE‐directed therapeutics. Tackling RAGE/mDia1 may identify a novel class of therapeutics preventing diabetes and its complications.</jats:p>
Journal
-
- Clinical Pharmacology & Therapeutics
-
Clinical Pharmacology & Therapeutics 98 (2), 135-144, 2015-06-25
Wiley
- Tweet
Details 詳細情報について
-
- CRID
- 1362825895371989376
-
- DOI
- 10.1002/cpt.148
-
- ISSN
- 15326535
- 00099236
-
- Data Source
-
- Crossref