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The wnt/beta-catenin pathway in wilms tumors and prostate cancers.

机译:Wnt /β-catenin途径在野生型肿瘤和前列腺癌中。

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摘要

Wnt/beta-catenin signaling is constitutively increased in several major classes of tumors arising from the urogenital tract. In this review we focus on this pathway mainly in Wilms tumors and prostate carcinomas, followed by a brief discussion of its potential role in other types of urological tumors. Molecular studies in these types of cancers have highlighted novel components upstream and downstream of this central oncogenic pathway. Beta-catenin gain-of-function mutations are strongly linked to WT1 loss-of-function mutations in syndromic Wilms tumors, and Wnt/beta-catenin signaling increases androgen receptor mRNA expression and blocks apoptosis in prostate cancers. Novel downstream target genes activated by Wnt/beta-catenin signaling are emerging from expression profiling in genetically defined classes of Wilms tumors, and similar analyses are expected to reveal additional downstream genes of this pathway specific to prostate cancers. The identities of these genes will likely suggest new targeted therapies for urological malignancies.
机译:Wnt /β-catenin信号在泌尿生殖道引起的几类主要肿瘤中组成性增加。在这篇综述中,我们主要关注该途径在威尔姆斯肿瘤和前列腺癌中的作用,然后简要讨论其在其他类型泌尿科肿瘤中的潜在作用。在这些类型的癌症中的分子研究突显了该中心致癌途径上游和下游的新成分。 β-catenin功能获得性突变与综合征性Wilms肿瘤中的WT1功能丧失突变紧密相关,Wnt /β-catenin信号传导增加雄激素受体mRNA表达并阻断前列腺癌的细胞凋亡。 Wnt /β-catenin信号激活的新型下游靶基因正从基因定义的Wilms肿瘤类别的表达谱中出现,并且类似的分析有望揭示该途径对前列腺癌具有特异性的其他下游基因。这些基因的身份可能会建议针对泌尿系统恶性肿瘤的新靶向疗法。

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