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Should SIX2 be routinely tested in patients with isolated congenital abnormalities of kidneys and/or urinary tract (CAKUT)?

作者信息

Faguer Stanislas, Chassaing Nicolas, Bandin Flavio, Prouheze Cathie, Chauveau Dominique, Decramer Stéphane

机构信息

Nephrology and Transplantation Department, University Hospital of Toulouse, Toulouse, France.

出版信息

Eur J Med Genet. 2012 Dec;55(12):688-9. doi: 10.1016/j.ejmg.2012.06.003. Epub 2012 Jul 15.

DOI:10.1016/j.ejmg.2012.06.003
PMID:22809486
Abstract

Mutations of the transcription factor SIX2 have been associated with renal hypodysplasia, renal cysts or vesicoureteric reflux. Here, we aimed at confirming the role and the prevalence of SIX2 mutations in a large cohort of 125 individuals with various congenital abnormalities of kidneys and urinary tract. Despite extensive sequencing of all exons and intron-exon boundaries, we failed to detect any SIX2 variation suggesting that SIX2 molecular analysis should not yet be recommended in clinical practice but restricted to research programs.

摘要

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Transcription factor Six2 induces a stem cell-like phenotype in renal cell carcinoma cells.转录因子Six2在肾癌细胞中诱导出一种干细胞样表型。
FEBS Open Bio. 2019 Oct;9(10):1808-1816. doi: 10.1002/2211-5463.12721. Epub 2019 Sep 19.
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COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans.COL4A1 突变可能是人类常染色体显性 CAKUT 的一个新病因。
Hum Genet. 2019 Oct;138(10):1105-1115. doi: 10.1007/s00439-019-02042-4. Epub 2019 Jun 22.
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Haploinsufficiency for the Six2 gene increases nephron progenitor proliferation promoting branching and nephron number.
Six2 基因部分缺失会增加肾祖细胞的增殖,促进分支和肾单位数量。
Kidney Int. 2018 Mar;93(3):589-598. doi: 10.1016/j.kint.2017.09.015. Epub 2017 Dec 6.