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异常甲基化介导的长链非编码RNA LOC100130476下调与食管鳞状细胞癌的恶性进展相关。

Aberrant methylation-mediated downregulation of long noncoding RNA LOC100130476 correlates with malignant progression of esophageal squamous cell carcinoma.

作者信息

Guo Wei, Dong Zhiming, Shi Yabin, Liu Shengnan, Liang Jia, Guo Yanli, Guo Xin, Shen Supeng, Shan Baoen

机构信息

Laboratory of Pathology, Hebei Cancer Institute, the Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.

Research Center, the Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.

出版信息

Dig Liver Dis. 2016 Aug;48(8):961-9. doi: 10.1016/j.dld.2016.05.010. Epub 2016 Jun 1.

Abstract

BACKGROUND

Dysregulated long non-coding RNAs (lncRNAs) are involved in many complicated human diseases including cancer.

AIMS

To determine the role and methylation status of a new lncRNA LOC100130476 in the pathogenesis of esophageal squamous cell carcinoma (ESCC).

METHODS

One hundred and twenty three ESCC patients with tumor tissues and corresponding adjacent normal tissues were enrolled. The expression level and methylation status of LOC100130476 in esophageal cancer cell lines and primary ESCC samples were respectively detected.

RESULTS

Significant downregulation of LOC100130476 was detected in esophageal cancer cell lines and primary ESCC tumor tissues. Up-regulation of LOC100130476 led to the inhibition of proliferation and invasiveness of the cancer cells. Aberrant hypermethylation of the CpG sites in exon 1 closing to the transcription start site was found to be more tumor-specific and to be more critical for gene silencing. Hypermethylation of these CpG sites was associated with TNM stage and pathological differentiation. ESCC patients in stage III and IV, with low expression or hypermethylation of the CpG sites in exon 1 demonstrated poor patient survival.

CONCLUSIONS

LOC100130476 is down-regulated in ESCC at least partly by hypermethylation of CpG sites in exon 1 and its hypermethylation may have prognostic implications for ESCC patients.

摘要

背景

长链非编码RNA(lncRNA)失调与包括癌症在内的许多复杂人类疾病有关。

目的

确定新型lncRNA LOC100130476在食管鳞状细胞癌(ESCC)发病机制中的作用及甲基化状态。

方法

招募123例患有肿瘤组织及相应癌旁正常组织的ESCC患者。分别检测食管癌细胞系及原发性ESCC样本中LOC100130476的表达水平和甲基化状态。

结果

在食管癌细胞系及原发性ESCC肿瘤组织中检测到LOC100130476显著下调。上调LOC100130476可导致癌细胞增殖和侵袭能力受到抑制。发现在靠近转录起始位点的外显子1中,CpG位点的异常高甲基化具有更多肿瘤特异性,且对基因沉默更为关键。这些CpG位点的高甲基化与TNM分期及病理分化相关。III期和IV期的ESCC患者,若外显子1中CpG位点低表达或高甲基化,则患者生存率较差。

结论

ESCC中LOC100130476下调至少部分是由于外显子1中CpG位点的高甲基化,其高甲基化可能对ESCC患者具有预后意义。

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