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由HOXA5调控的长链非编码RNA 00312抑制非小细胞肺癌中的肿瘤增殖并促进细胞凋亡。

Long non-coding RNA 00312 regulated by HOXA5 inhibits tumour proliferation and promotes apoptosis in Non-small cell lung cancer.

作者信息

Zhu Qingqing, Lv Tangfeng, Wu Ying, Shi Xuefei, Liu Hongbing, Song Yong

机构信息

Department of Respiratory Medicine, Jinling Hospital, Nanjing University School of Medicine, Nanjing, China.

Nanjing University Institute of Respiratory Medicine, Nanjing, China.

出版信息

J Cell Mol Med. 2017 Sep;21(9):2184-2198. doi: 10.1111/jcmm.13142. Epub 2017 Mar 24.

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.

摘要

非小细胞肺癌(NSCLC)是最常见的肺癌类型。已有报道称,许多长链非编码RNA(lncRNA)的异常表达参与了各种肿瘤的进展,其可作为诊断指标或抗肿瘤靶点。在此,我们发现长链非编码RNA 00312在配对的NSCLC组织中表达下调,且与不良临床预后相关;NSCLC中linc00312表达降低与更大且更晚期的肿瘤相关。功能实验表明,linc00312在体外和体内均可抑制细胞增殖并促进细胞凋亡。此外,我们发现HOXA5可结合在linc00312的启动子上并上调其表达。而且,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表达下调。综上所述,我们的研究结果表明,linc00312可能是NSCLC的一种新型诊断生物标志物和有前景的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a450/5571553/4b27d1b77deb/JCMM-21-2184-g001.jpg

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