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长链非编码RNA DLX6-AS1的上调通过靶向miR-577促进食管鳞状细胞癌的细胞生长和转移。

Upregulation of long noncoding RNA DLX6-AS1 promotes cell growth and metastasis in esophageal squamous cell carcinoma via targeting miR-577.

作者信息

Wu S-B, Wang H-Q

机构信息

Department of Gastroenterology, the Second Hospital of Dalian Medical University, Dalian, China.

出版信息

Eur Rev Med Pharmacol Sci. 2020 Feb;24(3):1195-1201. doi: 10.26355/eurrev_202002_20171.

Abstract

OBJECTIVE

Esophageal squamous cell carcinoma (ESCC) is the most malignant type of esophageal cancer. Although significant advances have been made in ESCC diagnosis and therapy, its poor pathogenesis and prognosis remain a life-threatening problem. Meanwhile, long noncoding RNAs (lncRNAs) exert a pivotal function in tumorigenesis. In this research, we aimed to explore the association between the aberrant expression of lncRNA DLX6-AS1 and the development and metastasis of ESCC.

PATIENTS AND METHODS

DLX6-AS1 expression was monitored by quantitative Real Time-Polymerase Chain Reaction (qRT-PCR) in ESCC specimens. Moreover, experiments were conducted to detect the effect of DLX6-AS1 on the cell proliferation and metastasis of ESCC. In addition, the underlying mechanism was further explored through luciferase assays and RNA immunoprecipitation assay (RIP).

RESULTS

DLX6-AS1 expression level was significantly higher in ESCC specimens. Moreover, cell proliferation and metastasis of ESCC cells could be inhibited via reducing DLX6-AS1 expression. Besides, DLX6-AS1 was regarded as an oncogene in ESCC. Furthermore, DLX6-AS1 acted as a competing endogenous RNA via sponging miR-577 in ESCC.

CONCLUSIONS

In summary, DLX6-AS1 promotes development and metastasis of ESCC by sponging miR-577 and could be a potential therapeutic target.

摘要

目的

食管鳞状细胞癌(ESCC)是食管癌中恶性程度最高的类型。尽管ESCC的诊断和治疗已取得显著进展,但其不良的发病机制和预后仍然是一个危及生命的问题。同时,长链非编码RNA(lncRNA)在肿瘤发生中发挥着关键作用。在本研究中,我们旨在探讨lncRNA DLX6-AS1的异常表达与ESCC发生发展及转移之间的关联。

患者和方法

通过定量实时聚合酶链反应(qRT-PCR)监测ESCC标本中DLX6-AS1的表达。此外,进行实验检测DLX6-AS1对ESCC细胞增殖和转移的影响。另外,通过荧光素酶报告基因检测和RNA免疫沉淀试验(RIP)进一步探究其潜在机制。

结果

ESCC标本中DLX6-AS1表达水平显著升高。此外,降低DLX6-AS1表达可抑制ESCC细胞的增殖和转移。此外,DLX6-AS1在ESCC中被视为癌基因。此外,在ESCC中,DLX6-AS1通过海绵吸附miR-577发挥竞争性内源RNA的作用。

结论

综上所述,DLX6-AS1通过海绵吸附miR-577促进ESCC的发生发展及转移,可能是一个潜在的治疗靶点。

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