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NAIF1 在胃癌中表达下调,并通过 caspase-9 通路促进人 MKN45 细胞凋亡。

NAIF1 is down-regulated in gastric cancer and promotes apoptosis through the caspase-9 pathway in human MKN45 cells.

机构信息

Department of Etiology and Carcinogenesis and State Key Laboratory of Molecular Oncology, Cancer Institute and Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, PR China.

出版信息

Oncol Rep. 2011 Apr;25(4):1117-23. doi: 10.3892/or.2011.1171. Epub 2011 Jan 31.

Abstract

Many key proteins are down-regulated or lose their function during cancer genesis and accelerate the progress of cancer. We found that nuclear apoptosis-inducing factor 1 (NAIF1) was highly expressed in normal gastric tissues but was down-regulated or lost in gastric cancer tissues (P<0.001). NAIF1 expression was higher in well-differentiated (P=0.004) than in moderately- or poorly-differentiated gastric cancer. NAIF1 expression was associated with different T stages (P=0.024). In vitro, NAIF1 can inhibit tumor cell proliferation and induce G0/G1 phase cell cycle arrest in the MKN45 cell line. NAIF1 can induce apoptosis through activation of procaspase-9 rather than procaspase-8 followed by activation of the caspase-3 pathway. We designed and constructed two truncation mutants, pEGFP-N1-NLS and pEGFP-N1-GRR, and identified the N-terminal 1-90 amino acid domain of NAIF1, which is a helix-turn-helix motif and which was sufficient for inducing apoptosis. Therefore, these findings suggest that NAIF1 plays an inhibitory role in the initial steps of gastric cancer genesis and may provide new strategies for developing anti-cancer drugs using small molecular polypeptides.

摘要

许多关键蛋白在癌症发生过程中下调或失去功能,从而加速癌症的进展。我们发现核凋亡诱导因子 1(NAIF1)在正常胃组织中高表达,但在胃癌组织中下调或丢失(P<0.001)。NAIF1 在高分化(P=0.004)胃癌中表达高于中分化或低分化胃癌。NAIF1 的表达与不同的 T 分期相关(P=0.024)。在体外,NAIF1 可抑制肿瘤细胞增殖,并在 MKN45 细胞系中诱导 G0/G1 期细胞周期阻滞。NAIF1 通过激活前胱冬肽酶-9而不是前胱冬肽酶-8,继而激活 caspase-3 途径诱导细胞凋亡。我们设计并构建了两个截断突变体,pEGFP-N1-NLS 和 pEGFP-N1-GRR,并鉴定了 NAIF1 的 N 端 1-90 个氨基酸结构域,该结构域是一个螺旋-转角-螺旋基序,足以诱导细胞凋亡。因此,这些发现表明,NAIF1 在胃癌发生的初始步骤中起抑制作用,可能为使用小分子多肽开发抗癌药物提供新的策略。

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