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首页> 外文期刊>Cell death & disease. >NORE1A induction by membrane-bound CD40L (mCD40L) contributes to CD40L-induced cell death and G1 growth arrest in p21-mediated mechanism
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NORE1A induction by membrane-bound CD40L (mCD40L) contributes to CD40L-induced cell death and G1 growth arrest in p21-mediated mechanism

机译:膜结合的CD40L(MCD40L)诱导诱导P21介导机制的CD40L诱导的细胞死亡和G1生长停滞

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Membrane-bound CD40L (mCD40L) but not soluble CD40L (sCD40L) has been implicated in direct cell death induction and apoptosis in CD40-expressing carcinomas. In this study, we show that mCD40L but not sCD40L induces NORE1A/Rassf5 expression in an NF κ B-dependant mechanism. NORE1A expression appeared to contribute to mCD40L-induced cell death and enhance cell transition from G1 to S phase of the cell cycle in a p21-dependent mechanism. The upregulation of p21 protein was attributed to NORE1A expression, since NORE1A inhibition resulted in p21 downregulation. p21 upregulation was concomitant with lower p53 expression in the cytoplasmic fraction with no detectable increase at the nuclear p53 level. Moreover, mCD40L-induced cell death mediated by NORE1A expression appeared to be independent of mCD40L-induced cell death mediated by sustained JNK activation since NORE1A inhibition did not affect JNK phosphorylation and vice versa. The presented data allow better understanding of the mechanism by which mCD40L induces cell death which could be exploited in the clinical development of CD40-targeted anti-cancer therapies.
机译:膜结合的CD40L(MCD40L)但不可溶的CD40L(SCD40L)涉及CD40表达癌中的直接细胞死亡诱导和细胞凋亡。在这项研究中,我们表明MCD40L但不是SCD40L在NFκB依赖机构中引起NORE1A / RASSF5表达。 NORE1A表达似乎有助于MCD40L诱导的细胞死亡,并在P21依赖性机制中提高来自细胞周期的G1至S期的细胞转变。 P21蛋白的上调归因于NORE1A表达,因为NORE1A抑制导致P21下调。 P21上调伴随着细胞质级分中的较低P53表达,核P53水平没有可检测的增加。此外,由于NORE1A抑制不影响JNK磷酸化,因此似乎与由持续的JNK活化介导的MCD40L诱导的细胞死亡介导的MCD40L诱导的细胞死亡似乎与MCD40L诱导的细胞死亡无关。呈现的数据允许更好地理解MCD40L诱导细胞死亡的机制,这可以在CD40靶向抗癌疗法的临床发展中被利用。

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