Institute of Human Genetics, Medical Faculty, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Institute for Stem Cell Research and Regenerative Medicine, Medical Faculty, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
PLoS One. 2023 Jan 23;18(1):e0270380. doi: 10.1371/journal.pone.0270380. eCollection 2023.
In order to get a better insight into the timing of WT1 mutant Wilms tumor development, we compared the gene expression profiles of nine established WT1 mutant Wilms tumor cell lines with published data from different kidney cell types during development. Publications describing genes expressed in nephrogenic precursor cells, ureteric bud cells, more mature nephrogenic epithelial cells and interstitial cell types were used. These studies uncovered that the WT1 mutant Wilms tumor cells lines express genes from the earliest nephrogenic progenitor cells, as well as from more differentiated nephron cells with the highest expression from the stromal/interstitial compartment. The expression of genes from all cell compartments points to an early developmental origin of the tumor in a common stem cell. Although variability of the expression of specific genes was evident between the cell lines the overall expression pattern was very similar. This is likely dependent on their different genetic backgrounds with distinct WT1 mutations and the absence/presence of mutant CTNNB1.
为了更深入地了解 WT1 突变型肾母细胞瘤的发生时间,我们将 9 种已建立的 WT1 突变型肾母细胞瘤细胞系的基因表达谱与不同发育阶段肾脏细胞类型的已发表数据进行了比较。使用了描述肾祖细胞、输尿管芽细胞、更成熟的肾上皮细胞和间质细胞类型中表达基因的出版物。这些研究表明,WT1 突变型肾母细胞瘤细胞系表达来自最早的肾祖细胞的基因,以及来自分化程度更高的肾单位细胞的基因,其中基质/间质区的表达最高。所有细胞区室的基因表达表明肿瘤起源于共同的干细胞,具有早期发育特征。尽管细胞系之间特定基因的表达存在可变性,但总体表达模式非常相似。这可能依赖于它们不同的遗传背景,具有不同的 WT1 突变和突变 CTNNB1 的缺失/存在。