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Nuclear receptor binding protein 1 correlates with better prognosis and induces caspase-dependent intrinsic apoptosis through the JNK signalling pathway in colorectal cancer

机译:核受体结合蛋白1与更好的预后相关,并通过结直肠癌的JNK信号通路诱导依赖性依赖性内在细胞凋亡

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Nuclear receptor binding protein 1 (NRBP1) is a ubiquitously expressed and highly conserved pseudokinase that has important roles in cellular homoeostasis. Despite recent advances in understanding the biology of NRBP1, the role of NRBP1 and its underlying mechanism in colorectal cancer (CRC) have not been fully elucidated. In the present study, we observed that NRBP1 expression levels were significantly reduced in CRC tissues compared with corresponding adjacent normal tissues, and high NRBP1 expression correlated with better prognosis in CRC. Overexpression of NRBP1 inhibited CRC cell proliferation and promoted apoptosis in vitro and in vivo. In contrast, knockdown of NRBP1 expression increased cell proliferation and decreased the percentage of apoptotic cells. Moreover, overexpression of NRBP1 activated caspase-dependent intrinsic apoptosis. In addition, we further discovered that NRBP1 regulated the apoptotic pathway through interaction with JNK. Finally, NRBP1 overexpression led to attenuated CRC growth in a xenograft mouse model. Our study illustrates the suppressor role of NRBP1 in CRC and provides a potential therapeutic target.
机译:核受体结合蛋白1(NRBP1)是一种普遍的表达和高度保守的伪转基因酶,其在细胞同性恋中具有重要作用。尽管最近理解NRBP1的生物学进展,但NRBP1及其潜在的结肠直肠癌(CRC)的作用尚未完全阐明。在本研究中,与相应的相邻正常组织相比,CRC组织中的NRBP1表达水平显着降低,并且具有更好的CRC预后相关的高NRBP1表达。 NRBP1的过表达抑制了CRC细胞增殖并在体外促进了细胞凋亡。相比之下,NRBP1表达的敲低增加了细胞增殖并降低了凋亡细胞的百分比。此外,过表达NRBP1活化的胱天蛋白酶依赖性内在细胞凋亡。此外,我们进一步发现NRBP1通过与JNK的相互作用调节凋亡途径。最后,NRBP1过表达导致异种移植小鼠模型中的CRC生长。我们的研究说明了NRBP1在CRC中的抑制作用,并提供了潜在的治疗目标。

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