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A PTCH1 Homolog Transcriptionally Activated by p53 Suppresses Hedgehog Signaling

机译:P53转录激活的PTCH1同性恋抑制了刺猬信号

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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:P53介导对DNA损伤和刺猬(HH)信号通路的反应各自在许多类型的人类癌症中均匀地赘言。在这里,我们描述了对肿瘤抑制基因PTCH1同源的P53靶基因,并且可以用作HH途径激活的阻遏物。 PTCH53(先前指定的PTCHD4)对体外P53的高度响应,并且是在不同TP53突变细胞系和人肿瘤的降低的水平下一致表达的少量基因中。通过G蛋白偶联受体Smo抑制PTCH53的表达抑制了Canonical HH信号。因此,PTCH53描绘了一种新颖的诱导途径,P53可以抑制致瘤HH信号。

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