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IGFBP7 Is Not Required for B-RAF-Induced Melanocyte Senescence

机译:B-RAF诱导的黑素细胞衰老不需要IGFBP7

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摘要

Induction of senescence permanently restricts cellular proliferation after oncogenic stimulation thereby acting as a potent barrier to tumor develop-ment. The relevant effector proteins may therefore be fundamental to cancer development. A recent study identified IGFBP7 as a secreted factor mediating melanocyte senescence induced by... oncogenic B-RAF, which is found commonly in cutaneous nevi. In contrast to the previous report, we demon-strate that B-RAF signaling does not induce IGFBP7 expression, nor the expression of the IGFBP7 targets, BNIP3L, SMARCB1, or PEA15, in human melanocytes or fibroblasts. We also found no corre-lation between B-RAF mutational status and IGFBP7 protein expression levels in 22 melanoma cell lines, 90 melanomas, and 46 benign nevi. Furthermore, using a lentiviral silencing strategy we show that B-RAF induces senescence in melanocytes and fibroblasts, irrespective of the presence of IGFBP7. Therefore, we conclude that the secreted protein IGFBP7 is dispensable for B-RAFv600E-induced senescence in human melanocytes.
机译:致癌性刺激后,衰老的诱导永久性地限制了细胞的增殖,从而成为肿瘤发展的有效屏障。因此,相关的效应蛋白可能是癌症发展的基础。最近的一项研究确定了IGFBP7是一种介导黑素致癌性B-RAF诱导的黑素细胞衰老的分泌因子,该因子常见于皮肤痣。与先前的报告相反,我们证明B-RAF信号在人黑素细胞或成纤维细胞中不诱导IGFBP7表达,也不诱导IGFBP7靶标,BNIP3L,SMARCB1或PEA15的表达。我们还没有发现22个黑色素瘤细胞系,90个黑色素瘤和46个良性痣中B-RAF突变状态与IGFBP7蛋白表达水平之间存在相关性。此外,使用慢病毒沉默策略,我们表明B-RAF可以诱导黑素细胞和成纤维细胞衰老,而与IGFBP7的存在无关。因此,我们得出结论,分泌蛋白IGFBP7对于B-RAFv600E诱导的人黑素细胞衰老是必不可少的。

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