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WT1基因在肾母细胞瘤和胚胎肾中的表达。

CITED1 expression in Wilms' tumor and embryonic kidney.

作者信息

Lovvorn Harold N, Westrup Jenifer, Opperman Shaun, Boyle Scott, Shi Genbin, Anderson James, Perlman Elizabeth J, Perantoni Alan O, Wills Marcia, de Caestecker Mark

机构信息

The Department of Pediatric Surgery, Vanderbilt University School of Medicine, Nashville, TN, USA.

出版信息

Neoplasia. 2007 Jul;9(7):589-600. doi: 10.1593/neo.07358.

Abstract

Wilms' tumors, or nephroblastomas, are thought to arise from abnormal postnatal retention and dysregulated differentiation of nephrogenic progenitor cells that originate as a condensed metanephric mesenchyme within embryonic kidneys. We have previously shown that the transcriptional regulator CITED1 (CBP/p300-interacting transactivators with glutamic acid [E]/aspartic acid [D]-rich C-terminal domain) is expressed exclusively in these nephrogenic progenitor cells and is downregulated as they differentiate to form nephronic epithelia. In the current study, we show that CITED1 expression persists in blastemal cell populations of both experimental rat nephroblastomas and human Wilms' tumors, and that primary human Wilms' tumors presenting with disseminated disease show the highest level of CITED1 expression. Unlike the predominantly cytoplasmic subcellular localization of CITED1 in the normal developing kidney, CITED1 is clearly detectable in the nuclear compartment of Wilms' tumor blastema. These findings indicate that CITED1 is a marker of primitive blastema in Wilms' tumors and suggest that persistent expression and/or altered subcellular localization of CITED1 in the condensed metanephric mesenchyme could play a role in Wilms' tumor initiation and pathogenesis.

摘要

肾母细胞瘤,又称肾胚胎瘤,被认为起源于肾源性祖细胞的异常产后存留和分化失调,这些祖细胞最初是胚胎肾内浓缩的后肾间充质。我们之前已经表明,转录调节因子CITED1(具有富含谷氨酸[E]/天冬氨酸[D]的C末端结构域的CBP/p300相互作用反式激活因子)仅在这些肾源性祖细胞中表达,并且在它们分化形成肾单位上皮时下调。在当前研究中,我们发现CITED1在实验性大鼠肾母细胞瘤和人类肾母细胞瘤的胚芽细胞群体中持续表达,并且呈现播散性疾病的原发性人类肾母细胞瘤显示出最高水平的CITED1表达。与CITED1在正常发育肾脏中主要定位于细胞质不同,在肾母细胞瘤胚芽的核区室中可清楚检测到CITED1。这些发现表明CITED1是肾母细胞瘤中原始胚芽的标志物,并提示CITED1在浓缩的后肾间充质中持续表达和/或亚细胞定位改变可能在肾母细胞瘤的起始和发病机制中起作用。

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