Literature DB >> 33998596

DACH1 as a multifaceted and potentially druggable susceptibility factor for kidney disease.

Sandra Merscher1,2, Christian Faul3.   

Abstract

Kidney diseases affect more than 15% of adults in the US, yet drug development in the kidney field, when compared with that for other common diseases, has been lagging behind. Modifiers that increase the susceptibility to injury and contribute to the pathogenesis and progression of kidney disease include genetic and environmental factors and epigenetic mechanisms. In this issue of the JCI, Cao et al. and Doke et al. independently report the identification of a susceptibility factor called Dachshund homolog 1 (DACH1). Both groups identify an association of reduced DACH1 expression with kidney disease, using different screening approaches, studying different types of human kidney diseases, and using different experimental models, making the fact that both stumbled over the same protein very compelling. Combined, these studies highlight DACH1 as a key safeguard in the kidney, granting various cell types proper function by modulating several molecular pathways.

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Year:  2021        PMID: 33998596      PMCID: PMC8121511          DOI: 10.1172/JCI149043

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   19.456


  14 in total

Review 1.  Epigenetics and epigenomics in diabetic kidney disease and metabolic memory.

Authors:  Mitsuo Kato; Rama Natarajan
Journal:  Nat Rev Nephrol       Date:  2019-06       Impact factor: 28.314

2.  Dach1 mutant mice bear no gross abnormalities in eye, limb, and brain development and exhibit postnatal lethality.

Authors:  R J Davis; W Shen; Y I Sandler; M Amoui; P Purcell; R Maas; C N Ou; H Vogel; A L Beaudet; G Mardon
Journal:  Mol Cell Biol       Date:  2001-03       Impact factor: 4.272

3.  miR-218 inhibits glucose metabolism in non-small cell lung cancer via the NF-κB signaling pathway.

Authors:  Wenxian Tian; Xiangfei Yuan; Yongna Song; Jianxia Zhai; Haixia Wei; Linna Wang; Dan Li; Qiusheng Chen
Journal:  Exp Ther Med       Date:  2020-11-27       Impact factor: 2.447

4.  A genome-wide association study for diabetic nephropathy genes in African Americans.

Authors:  Caitrin W McDonough; Nicholette D Palmer; Pamela J Hicks; Bong H Roh; S Sandy An; Jessica N Cooke; Jessica M Hester; Maria R Wing; Meredith A Bostrom; Megan E Rudock; Joshua P Lewis; Matthew E Talbert; Rebecca A Blevins; Lingyi Lu; Maggie C Y Ng; Michele M Sale; Jasmin Divers; Carl D Langefeld; Barry I Freedman; Donald W Bowden
Journal:  Kidney Int       Date:  2010-12-08       Impact factor: 10.612

5.  Impaired interactions between mouse Eyal harboring mutations found in patients with branchio-oto-renal syndrome and Six, Dach, and G proteins.

Authors:  Hidenori Ozaki; Yoko Watanabe; Keiko Ikeda; Kiyoshi Kawakami
Journal:  J Hum Genet       Date:  2002       Impact factor: 3.172

6.  Double homozygous missense mutations in DACH1 and BMP4 in a patient with bilateral cystic renal dysplasia.

Authors:  Raphael Schild; Tanja Knüppel; Martin Konrad; Carsten Bergmann; Agnes Trautmann; Markus J Kemper; Kongming Wu; Sergey Yaklichkin; Jing Wang; Richard Pestell; Dirk E Müller-Wiefel; Franz Schaefer; Stefanie Weber
Journal:  Nephrol Dial Transplant       Date:  2012-12-21       Impact factor: 5.992

7.  Podocyte-specific RAP1GAP expression contributes to focal segmental glomerulosclerosis-associated glomerular injury.

Authors:  Uma Potla; Jie Ni; Justin Vadaparampil; Guozhe Yang; Jeremy S Leventhal; Kirk N Campbell; Peter Y Chuang; Alexei Morozov; John C He; Vivette D D'Agati; Paul E Klotman; Lewis Kaufman
Journal:  J Clin Invest       Date:  2014-03-18       Impact factor: 14.808

8.  Decreased DACH1 expression in glomerulopathy is associated with disease progression and severity.

Authors:  Qing-Quan Liu; Ya-Qun Zhou; Hui-Quan Liu; Wen-Hui Qiu; Hui Liu; Ting-Yang Hu; Qing Xu; Yong-Man Lv; Kong-Ming Wu
Journal:  Oncotarget       Date:  2016-12-27

9.  A Multi-layered Quantitative In Vivo Expression Atlas of the Podocyte Unravels Kidney Disease Candidate Genes.

Authors:  Markus M Rinschen; Markus Gödel; Florian Grahammer; Stefan Zschiedrich; Martin Helmstädter; Oliver Kretz; Mostafa Zarei; Daniela A Braun; Sebastian Dittrich; Caroline Pahmeyer; Patricia Schroder; Carolin Teetzen; HeonYung Gee; Ghaleb Daouk; Martin Pohl; Elisa Kuhn; Bernhard Schermer; Victoria Küttner; Melanie Boerries; Hauke Busch; Mario Schiffer; Carsten Bergmann; Marcus Krüger; Friedhelm Hildebrandt; Joern Dengjel; Thomas Benzing; Tobias B Huber
Journal:  Cell Rep       Date:  2018-05-22       Impact factor: 9.423

10.  DACH1, a novel target of miR-218, participates in the regulation of cell viability, apoptosis, inflammatory response, and epithelial-mesenchymal transition process in renal tubule cells treated by high-glucose.

Authors:  Ying-Li Zhang; Jie-Min Wang; Hong Yin; Shou-Bao Wang; Cai-Ling He; Jing Liu
Journal:  Ren Fail       Date:  2020-11       Impact factor: 2.606

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