首页> 外文期刊>The Journal of biological chemistry >KAI1 Gene Is Engaged in NDRG1 Gene-mediated Metastasis Suppression through the ATF3-NFκB Complex in Human Prostate Cancer
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KAI1 Gene Is Engaged in NDRG1 Gene-mediated Metastasis Suppression through the ATF3-NFκB Complex in Human Prostate Cancer

机译:Kai1基因通过人前列腺癌的ATF3-NFκB络合物从事NDRG1基因介导的转移抑制

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NDRG1 and KAI1 belong to metastasis suppressor genes, which impede the dissemination of tumor cells from primary tumors to distant organs. Previously, we identified the metastasis promoting transcription factor, ATF3, as a downstream target of NDRG1. Further analysis revealed that the KAI1 promoter contained a consensus binding motif of ATF3, suggesting a possibility that NDRG1 suppresses metastasis through inhibition of ATF3 expression followed by activation of the KAI1 gene. In this report, we found that ectopic expression of NDRG1 was able to augment endogenous KAI1 gene expression in prostate cancer cell lines, whereas silencing NDRG1 was accompanied with significant decrease in KAI1 expression in vitro and in vivo. In addition, our results of ChIP analysis indicate that ATF3 indeed bound to the promoter of the KAI1 gene. Importantly, our promoter-based analysis revealed that ATF3 modulated KAI1 transcription through cooperation with other endogenous transcription factor as co-activator (ATF3-JunB) or co-repressor (ATF3-NFκB). Moreover, loss of KAI1 expression significantly abrogated NDRG1-mediated metastatic suppression in vitro as well as in a spontaneous metastasis animal model, indicating that KA11 is a functional downstream target of the NDRG1 pathway. Our result of immunohistochemical analysis showed that loss of NDRG1 and KAI1 occurs in parallel as prostate cancer progresses. We also found that a combined expression status of these two genes serves as a strong independent prognostic marker to predict metastasis-free survival of prostate cancer patients. Taken together, our result revealed a novel regulatory network of two metastasis suppressor genes, NDRG1 and KAI1, which together concerted metastasis-suppressive activities through an intrinsic transcriptional cascade.
机译:NDRG1和Kai1属于转移抑制基因,其妨碍肿瘤细胞从原发性肿瘤传播到远处的器官。以前,我们鉴定了促进转录因子ATF3的转移作为NDRG1的下游靶标。进一步的分析表明,Kai1启动子含有ATF3的共有结合基质,表明NDRG1通过抑制ATF3表达,然后激活Kai1基因的可能性。在本报告中,我们发现NDRG1的异位表达能够在前列腺癌细胞中增加内源性Kai1基因表达,而沉默的NDRG1伴随着体外和体内Kai1表达的显着降低。此外,我们的芯片分析结果表明ATF3确实与KAI1基因的启动子结合。重要的是,我们的启动子的分析显示ATF3通过与其他内源转录因子作为共激活剂(ATF3-JONB)或Co-re-Reincor(ATF3-NFκB)的合作进行调节的Kai1转录。此外,在体外,Kai1表达的丧失显着消除了NDRG1介导的转移性抑制,以及在自发转移动物模型中,表明KA11是NDRG1途径的功能下游靶。我们的免疫组织化学分析结果表明,随着前列腺癌的进展并行地发生NDRG1和Kai1。我们还发现,这两个基因的组合表达状态是强烈的独立预后标志物,以预测前列腺癌患者的无转移存活。我们的结果揭示了两种转移抑制基因,NDRG1和Kai1的新型调节网络,其通过内在转录级联统一抑制活性。

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