Literature DB >> 24461730

New insights into molecular mechanisms of diabetic kidney disease.

Shawn S Badal1, Farhad R Danesh2.   

Abstract

Diabetic kidney disease remains a major microvascular complication of diabetes and the most common cause of chronic kidney failure requiring dialysis in the United States. Medical advances over the past century have substantially improved the management of diabetes mellitus and thereby have increased patient survival. However, current standards of care reduce but do not eliminate the risk of diabetic kidney disease, and further studies are warranted to define new strategies for reducing the risk of diabetic kidney disease. In this review, we highlight some of the novel and established molecular mechanisms that contribute to the development of the disease and its outcomes. In particular, we discuss recent advances in our understanding of the molecular mechanisms implicated in the pathogenesis and progression of diabetic kidney disease, with special emphasis on the mitochondrial oxidative stress and microRNA targets. Additionally, candidate genes associated with susceptibility to diabetic kidney disease and alterations in various cytokines, chemokines, and growth factors are addressed briefly.
Copyright © 2014 National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  End-stage renal disease (ESRD); diabetes mellitus; diabetic kidney disease; pathogenesis

Mesh:

Substances:

Year:  2014        PMID: 24461730      PMCID: PMC3932114          DOI: 10.1053/j.ajkd.2013.10.047

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


  231 in total

1.  Mitochondrial H2O2 regulates the angiogenic phenotype via PTEN oxidation.

Authors:  Kip M Connor; Sita Subbaram; Kevin J Regan; Kristin K Nelson; Joseph E Mazurkiewicz; Peter J Bartholomew; Andrew E Aplin; Yu-Tzu Tai; Julio Aguirre-Ghiso; Sonia C Flores; J Andres Melendez
Journal:  J Biol Chem       Date:  2005-02-08       Impact factor: 5.157

2.  The low molecular weight GTPase Rho regulates myofibril formation and organization in neonatal rat ventricular myocytes. Involvement of Rho kinase.

Authors:  M Hoshijima; V P Sah; Y Wang; K R Chien; J H Brown
Journal:  J Biol Chem       Date:  1998-03-27       Impact factor: 5.157

3.  Overexpression of Cu2+/Zn2+ superoxide dismutase protects against early diabetic glomerular injury in transgenic mice.

Authors:  P A Craven; M F Melhem; S L Phillips; F R DeRubertis
Journal:  Diabetes       Date:  2001-09       Impact factor: 9.461

4.  Overexpression of VEGF-A in podocytes of adult mice causes glomerular disease.

Authors:  Delma Veron; Kimberly J Reidy; Claudia Bertuccio; Jason Teichman; Guillermo Villegas; Juan Jimenez; Wa Shen; Jeffrey B Kopp; David B Thomas; Alda Tufro
Journal:  Kidney Int       Date:  2010-03-10       Impact factor: 10.612

5.  A Rho-kinase inhibitor, fasudil, prevents development of diabetes and nephropathy in insulin-resistant diabetic rats.

Authors:  Yuichi Kikuchi; Muneharu Yamada; Toshihiko Imakiire; Taketoshi Kushiyama; Keishi Higashi; Naomi Hyodo; Kojiro Yamamoto; Takashi Oda; Shigenobu Suzuki; Soichiro Miura
Journal:  J Endocrinol       Date:  2007-03       Impact factor: 4.286

6.  Vascular permeability factor mRNA and protein expression in human kidney.

Authors:  L F Brown; B Berse; K Tognazzi; E J Manseau; L Van de Water; D R Senger; H F Dvorak; S Rosen
Journal:  Kidney Int       Date:  1992-12       Impact factor: 10.612

7.  Development of type 2 diabetes following intrauterine growth retardation in rats is associated with progressive epigenetic silencing of Pdx1.

Authors:  Jun H Park; Doris A Stoffers; Robert D Nicholls; Rebecca A Simmons
Journal:  J Clin Invest       Date:  2008-06       Impact factor: 14.808

8.  Targeting of RhoA/ROCK signaling ameliorates progression of diabetic nephropathy independent of glucose control.

Authors:  Vasantha Kolavennu; Lixia Zeng; Hui Peng; Yin Wang; Farhad R Danesh
Journal:  Diabetes       Date:  2007-12-14       Impact factor: 9.461

9.  Prevention of diabetic nephropathy by sulforaphane: possible role of Nrf2 upregulation and activation.

Authors:  Wenpeng Cui; Yang Bai; Xiao Miao; Ping Luo; Qiang Chen; Yi Tan; Madhavi J Rane; Lining Miao; Lu Cai
Journal:  Oxid Med Cell Longev       Date:  2012-09-23       Impact factor: 6.543

10.  Lymphocytes from patients with type 1 diabetes display a distinct profile of chromatin histone H3 lysine 9 dimethylation: an epigenetic study in diabetes.

Authors:  Feng Miao; David D Smith; Lingxiao Zhang; Andrew Min; Wei Feng; Rama Natarajan
Journal:  Diabetes       Date:  2008-09-05       Impact factor: 9.461

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  75 in total

Review 1.  Pathophysiology of diabetic kidney disease: impact of SGLT2 inhibitors.

Authors:  Ralph A DeFronzo; W Brian Reeves; Alaa S Awad
Journal:  Nat Rev Nephrol       Date:  2021-02-05       Impact factor: 28.314

2.  A breath of fresh air for diabetic nephropathy.

Authors:  Volker H Haase
Journal:  J Am Soc Nephrol       Date:  2014-09-02       Impact factor: 10.121

3.  MicroRNA-687 Induced by Hypoxia-Inducible Factor-1 Targets Phosphatase and Tensin Homolog in Renal Ischemia-Reperfusion Injury.

Authors:  Kirti Bhatt; Qingqing Wei; Navjotsingh Pabla; Guie Dong; Qing-Sheng Mi; Mingyu Liang; Changlin Mei; Zheng Dong
Journal:  J Am Soc Nephrol       Date:  2015-01-13       Impact factor: 10.121

Review 4.  Mitochondria Damage and Kidney Disease.

Authors:  Pu Duann; Pei-Hui Lin
Journal:  Adv Exp Med Biol       Date:  2017       Impact factor: 2.622

5.  Podocyte and endothelial-specific elimination of BAMBI identifies differential transforming growth factor-β pathways contributing to diabetic glomerulopathy.

Authors:  Han Lai; Anqun Chen; Hong Cai; Jia Fu; Fadi Salem; Yu Li; John C He; Detlef Schlondorff; Kyung Lee
Journal:  Kidney Int       Date:  2020-04-26       Impact factor: 10.612

6.  Association of kidney structure-related gene variants with type 2 diabetes-attributed end-stage kidney disease in African Americans.

Authors:  Meijian Guan; Jun Ma; Jacob M Keaton; Latchezar Dimitrov; Poorva Mudgal; Mary Stromberg; Jason A Bonomo; Pamela J Hicks; Barry I Freedman; Donald W Bowden; Maggie C Y Ng
Journal:  Hum Genet       Date:  2016-07-26       Impact factor: 4.132

7.  Baicalin reversal of DNA hypermethylation-associated Klotho suppression ameliorates renal injury in type 1 diabetic mouse model.

Authors:  Xiao-Tan Zhang; Guang Wang; Liu-Fang Ye; Yu Pu; Run-Tong Li; Jianxin Liang; Lijun Wang; Kenneth Ka Ho Lee; Xuesong Yang
Journal:  Cell Cycle       Date:  2020-11-16       Impact factor: 4.534

8.  The inhibition of SGK1 suppresses epithelial-mesenchymal transition and promotes renal tubular epithelial cell autophagy in diabetic nephropathy.

Authors:  Langen Zhuang; Guoxi Jin; Xiaolei Hu; Qingqing Yang; Zhaoming Shi
Journal:  Am J Transl Res       Date:  2019-08-15       Impact factor: 4.060

Review 9.  Acute Kidney Injury and Progression of Diabetic Kidney Disease.

Authors:  Samuel Mon-Wei Yu; Joseph V Bonventre
Journal:  Adv Chronic Kidney Dis       Date:  2018-03       Impact factor: 3.620

Review 10.  Mitochondrial dysfunction in diabetic kidney disease.

Authors:  Josephine M Forbes; David R Thorburn
Journal:  Nat Rev Nephrol       Date:  2018-02-19       Impact factor: 28.314

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