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首页> 外文期刊>Cell death & disease. >CUL1 promotes breast cancer metastasis through regulating EZH2-induced the autocrine expression of the cytokines CXCL8 and IL11
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CUL1 promotes breast cancer metastasis through regulating EZH2-induced the autocrine expression of the cytokines CXCL8 and IL11

机译:CUL1通过调节EZH2诱导细胞因子CXCL8和IL11的自分泌表达来促进乳腺癌转移

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摘要

CUL1 is an essential component of SCF (SKP1-CUL1-F-box protein) E3 ubiquitin ligase complex. Our previous study has showed that CUL1 is positively associated with poor overall and disease-specific survival of breast cancer patients. Here, we further explored its roles in breast cancer metastasis. Our data showed that CUL1 significantly promoted breast cancer cell migration, invasion, tube formation in vitro, as well as angiogenesis and metastasis in vivo. In mechanism, the human gene expression profiling was used to determine global transcriptional changes in MDA-MB-231 cells, and we identified autocrine expression of the cytokines CXCL8 and IL11 as the target genes of CUL1 in breast cancer cell migration, invasion, metastasis, and angiogenesis. CUL1 regulated EZH2 expression to promote the production of cytokines, and finally significantly aggravating the breast cancer cell metastasis and angiogenesis through the PI3K–AKT–mTOR signaling pathway. Combined with the previous report about CUL1, we proposed that CUL1 may serve as a promising therapeutic target for breast cancer metastasis.
机译:CUL1是SCF(SKP1-CUL1-F-box蛋白)E3泛素连接酶复合物的重要组成部分。我们以前的研究表明,CUL1与乳腺癌患者总体生存状况和疾病特异性生存率呈正相关。在这里,我们进一步探讨了其在乳腺癌转移中的作用。我们的数据显示,CUL1在体外显着促进乳腺癌细胞迁移,侵袭,管形成以及体内血管生成和转移。在机制上,人类基因表达谱用于确定MDA-MB-231细胞中的整体转录变化,并且我们确定细胞因子CXCL8和IL11的自分泌表达是乳腺癌细胞迁移,侵袭,转移,和血管生成。 CUL1调节EZH2的表达以促进细胞因子的产生,并最终通过PI3K–AKT–mTOR信号通路显着加重乳腺癌细胞的转移和血管生成。结合先前有关CUL1的报告,我们提出CUL1可以作为乳腺癌转移的有希望的治疗靶点。

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