首页> 外文期刊>Journal of cellular and molecular medicine. >Long non‐coding RNA 00312 regulated by HOXA5 inhibits tumour proliferation and promotes apoptosis in Non‐small cell lung cancer
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Long non‐coding RNA 00312 regulated by HOXA5 inhibits tumour proliferation and promotes apoptosis in Non‐small cell lung cancer

机译:HOXA5调控的长非编码RNA 00312抑制非小细胞肺癌的肿瘤增殖并促进细胞凋亡

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Abstract Non-small cell lung cancer (NSCLC) is the most prevalent type of lung cancer. The abnormal expression of many long non-coding RNAs (lncRNAs) has been reported involved in the progression of various tumours, which can be used as diagnostic indicators or antitumour targets. Here, we found that the long non-coding RNA 00312 was down-regulated in paired NSCLC tissues and correlated with poor clinical outcome; decreased linc00312 expression in NSCLC was associated with larger and later stage tumours. Functional experiments showed that linc00312 could inhibit cell proliferation and promote apoptosis in vitro and in vivo . Furthermore, we found that HOXA5 could bind in the promoter of linc00312 and up-regulated the expression of it. Moreover, linc00312 was down-regulated in the plasma of NSCLC patients compared with that of healthy volunteers or other pulmonary diseases patients. Taken together, our findings indicated that linc00312 could be a novel diagnosis biomarker and a promising therapeutic target for NSCLC.
机译:摘要非小细胞肺癌(NSCLC)是最普遍的肺癌类型。已经报道了许多长的非编码RNA(lncRNA)的异常表达与各种肿瘤的进展有关,这些肿瘤可以用作诊断指标或抗肿瘤靶标。在这里,我们发现长的非编码RNA 00312在成对的NSCLC组织中被下调,并且与不良的临床预后相关。 NSCLC中linc00312表达的降低与更大,更晚期的肿瘤有关。功能实验表明,linc00312在体内外均可抑制细胞增殖,促进细胞凋亡。此外,我们发现HOXA5可以结合在linc00312的启动子中,并上调其表达。此外,与健康志愿者或其他肺部疾病患者相比,NSCLC患者血浆中的linc00312被下调。综上所述,我们的发现表明linc00312可能是一种新颖的诊断生物标志物,并且有望成为NSCLC的治疗靶标。

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