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首页> 外文期刊>BMB Reports >Adenovirus vector-mediated FAM176A overexpression induces cell death in human H1299 non-small cell lung cancer cells
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Adenovirus vector-mediated FAM176A overexpression induces cell death in human H1299 non-small cell lung cancer cells

机译:腺病毒载体介导的FAM176A过表达诱导人H1299非小细胞肺癌细胞中的细胞死亡

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FAM176A (family with sequence similarity 176 member A) is a novel molecule related to programmed cell death. A decreased expression of FAM176A has been found in several types of human tumors in including lung cancers. In the present study, we investigated the biological activities of FAM176A on the human non?small cell lung cancer cell line H1299 cells. We constructed a recombinant adenovirus 5-FAM176A vector (Ad5-FAM176A) and evaluated the expression and anti-tumor activities in vitro. Cell viability analysis revealed that the adenovirus-mediated increase of FAM176A inhibited the growth of the tumor cells in a dose- and time-dependent manner. This inhibitory effect was mediated by both autophagy and apoptosis that involved caspase activation. In addition, cell cycle analysis suggested that Ad5-FAM176A could induce cell cycle arrest at the G2/M phase, all of which suggested that adenovirus-mediated FAM176A gene transfer might present a new therapeutic approach for lung cancer treatment.
机译:FAM176A(具有序列相似性176成员A的家庭)是与编程细胞死亡有关的新型分子。在包括肺癌中的几种类型的人肿瘤中发现了FAM176a的表达减少。在本研究中,我们调查了对人非?小细胞肺癌细胞系H1299细胞的FAM176A的生物活性。我们构建了重组腺病毒5-FAM176A载体(AD5-FAM176A),并在体外评估表达和抗肿瘤活性。细胞活力分析表明,腺病毒介导的FAM176A的增加抑制了肿瘤细胞以剂量和时间依赖性的方式的生长。这种抑制作用是通过伴有胱天蛋白酶活化的自噬和凋亡的介导的。此外,细胞循环分析表明,AD5-FAM176A可以在G2 / M阶段诱导细胞周期停滞,所有这些都表明腺病毒介导的FAM176A基因转移可能为肺癌治疗产生新的治疗方法。

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