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RETRACTED ARTICLE: Liver X receptors constrain tumor development and metastasis dissemination in PTEN-deficient prostate cancer

机译:缩回文章:肝X受体限制PTEN缺陷型前列腺癌的肿瘤发展和转移扩散

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摘要

Advanced prostate cancer (PCa) is a clinical challenge as no curative therapeutic is available. In this context, a better understanding of metastasis and resistance mechanisms in PCa is an important issue. As phosphatase and tensin homolog (PTEN) loss is the most common genetic lesion in such cancer, we investigate human data sets for mechanisms that can constrain cancer evolution in this setting. Here we report a liver X receptor (LXR) signature, which tightly correlates with PTEN loss, in PCa. Accordingly, the LXR pathway is deregulated in prostate carcinomas in Pten-null mice. Genetic ablation of LXRs in Pten-null mice, exacerbates PCa invasiveness and metastatic dissemination, which involves mesenchymal transition and accumulation of matrix metalloproteinases. Mechanistically, PTEN deletion governed LXR transcriptional activity through deregulation of cholesterol de novo synthesis, resulting in accumulation of endogenous LXR ligands. Our study therefore reveals a functional circuit linking PTEN and LXR, and highlights LXRs as metabolic gatekeepers that are able to constrain PCa progression.
机译:晚期前列腺癌(PCa)是临床难题,因为尚无治疗方法。在这种情况下,更好地了解PCa中的转移和耐药机制是一个重要问题。由于磷酸酶和张力蛋白同源物(PTEN)的丢失是此类癌症中最常见的遗传病灶,因此我们调查了人类数据集,寻找可以限制这种情况下癌症演变的机制。在这里,我们报告肝X受体(LXR)签名,与PCa中的PTEN丢失紧密相关。因此,在Pten-null小鼠的前列腺癌中LXR途径被失调。 Pten无小鼠的LXR的遗传消融加剧了PCa的侵袭性和转移性传播,这涉及间充质转化和基质金属蛋白酶的积累。从机制上讲,PTEN缺失通过重新调节胆固醇从头合成来控制LXR转录活性,导致内源性LXR配体的积累。因此,我们的研究揭示了连接PTEN和LXR的功能电路,并强调了LXRs作为能够限制PCa进程的代谢性关守者。

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