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首页> 外文期刊>Nature Communications >CDK4/6-dependent activation of DUB3 regulates cancer metastasis through SNAIL1
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CDK4/6-dependent activation of DUB3 regulates cancer metastasis through SNAIL1

机译:CDK4 / 6依赖的DUB3激活通过SNAIL1调节癌症转移

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摘要

Tumour metastasis, the spread of cancer cells from the original tumour site followed by growth of secondary tumours at distant organs, is the primary cause of cancer-related deaths and remains poorly understood. Here we demonstrate that inhibition of CDK4/6 blocks breast tumour metastasis in the triple-negative breast cancer model, without affecting tumour growth. Mechanistically, we identify a deubiquitinase, DUB3, as a target of CDK4/6; CDK4/6-mediated activation of DUB3 is essential to deubiquitinate and stabilize SNAIL1, a key factor promoting epithelial–mesenchymal transition and breast cancer metastasis. Overall, our study establishes the CDK4/6–DUB3 axis as an important regulatory mechanism of breast cancer metastasis and provides a rationale for potential therapeutic interventions in the treatment of breast cancer metastasis.
机译:肿瘤转移是癌细胞从原始肿瘤部位扩散,然后继发性肿瘤在远处器官生长,是癌症相关死亡的主要原因,目前仍知之甚少。在这里,我们证明了CDK4 / 6的抑制作用可在三阴性乳腺癌模型中阻止乳腺癌肿瘤转移,而不会影响肿瘤的生长。从机理上讲,我们将去泛素化酶DUB3鉴定为CDK4 / 6的靶标。 CDK4 / 6介导的DUB3激活对于去泛素化和稳定SNAIL1是必不可少的,SNAIL1是促进上皮-间质转化和乳腺癌转移的关键因素。总体而言,我们的研究将CDK4 / 6–DUB3轴确立为乳腺癌转移的重要调控机制,并为治疗乳腺癌转移的潜在治疗性干预措施提供了依据。

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