首页> 美国卫生研究院文献>Oncology Letters >Knockdown of high mobility group box 3 impairs cell viability and colony formation but increases apoptosis in A549 human non-small cell lung cancer cells
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Knockdown of high mobility group box 3 impairs cell viability and colony formation but increases apoptosis in A549 human non-small cell lung cancer cells

机译:敲低高迁移率族框3损害细胞活力和集落形成但增加A549人非小细胞肺癌细胞的凋亡

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摘要

Previous research has linked high mobility group box 3 (HMGB3) overexpression to the malignant progression and poor prognosis of non-small cell lung cancer (NSCLC). The present study investigated the role of HMGB3 in cell survival and colony formation of NSCLC cells. Stable knockdown of HMGB3 in A549 cells was achieved by lentiviral-based shRNA interference and verified by detection of the transcriptional and translational level of HMGB3 with reverse transcription-quantitative polymerase chain reaction and western blotting, respectively. The influence of HMGB3 knockdown on A549 cell viability and apoptotic rate was evaluated by Cell Counting Kit-8 assay and flow cytometry following annexin V staining, respectively. The proliferative capacity of A549 cells with or without HMGB3 knockdown was compared by measuring their colony forming efficiency. The results of the current study revealed that HMGB3 knockdown significantly reduced cell viability and colony forming efficiency while promoting apoptosis in A549 cells, indicating that HMGB3 may be pivotal for the survival and colony formation of A549 cells, serving a notable role in NSCLC progression.
机译:先前的研究已将高迁移率第3格盒(HMGB3)的过表达与非小细胞肺癌(NSCLC)的恶性进展和不良预后联系起来。本研究调查了HMGB3在NSCLC细胞存活和集落形成中的作用。 HMGB3在A549细胞中的稳定敲低是通过基于慢病毒的shRNA干扰实现的,并通过分别用逆转录定量聚合酶链反应和western印迹检测HMGB3的转录和翻译水平来验证。在膜联蛋白V染色后,分别通过Cell Counting Kit-8分析和流式细胞术评估HMGB3敲低对A549细胞活力和凋亡率的影响。通过测量其集落形成效率比较具有或不具有HMGB3敲低的A549细胞的增殖能力。当前研究的结果表明,HMGB3敲低显着降低了细胞活力和集落形成效率,同时促进了A549细胞的凋亡,这表明HMGB3可能对A549细胞的存活和集落形成至关重要,在NSCLC进程中起着重要作用。

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