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A PTCH1 Homolog Transcriptionally Activated by p53 Suppresses Hedgehog Signaling

机译:由p53转录激活的PTCH1同源物抑制了刺猬信号。

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摘要

The p53-mediated responses to DNA damage and the Hedgehog (Hh) signaling pathway are each recurrently dysregulated in many types of human cancer. Here we describe PTCH53, a p53 target gene that is homologous to the tumor suppressor gene PTCH1 and can function as a repressor of Hh pathway activation. PTCH53 (previously designated PTCHD4) was highly responsive to p53 in vitro and was among a small number of genes that were consistently expressed at reduced levels in diverse TP53 mutant cell lines and human tumors. Increased expression of PTCH53 inhibited canonical Hh signaling by the G protein-coupled receptor SMO. PTCH53 thus delineates a novel, inducible pathway by which p53 can repress tumorigenic Hh signals.
机译:在许多类型的人类癌症中,p53介导的对DNA损伤和Hedgehog(Hh)信号通路的应答均反复失调。在这里,我们描述了PTCH53,这是一种与肿瘤抑制基因PTCH1同源的p53靶基因,可以作为Hh途径激活的阻遏物。 PTCH53(以前称为PTCHD4)在体外对p53高度敏感,属于少数在不同TP53突变细胞系和人类肿瘤中始终以降低的水平表达的基因之一。 PTCH53的表达增加抑制了G蛋白偶联受体SMO的经典Hh信号传导。因此,PTCH53描绘了一种新颖的可诱导途径,p53可以通过该途径抑制致瘤性Hh信号。

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