下调和上调
岩石1
癌症研究
表皮生长因子受体
细胞
细胞生长
生物
细胞迁移
基因敲除
细胞凋亡
转移
医学
细胞周期
癌基因
小RNA
癌症
食管癌
内科学
细胞生物学
基因
激酶
蛋白激酶A
生物化学
遗传学
作者
Zhi Gang Feng,Xu Li,Minglian Qiu,Rong-gang Luo,Jonathan Feng-Shun Lin,Bo Liu
出处
期刊:Cancer Biotherapy and Radiopharmaceuticals
[Mary Ann Liebert]
日期:2020-02-05
卷期号:35 (1): 66-71
被引量:11
标识
DOI:10.1089/cbr.2019.2926
摘要
Background: EGFR-AS1 has been characterized as an oncogenic lncRNA in many types of cancers, while its roles in esophageal squamous cell carcinoma (ESCC) are unknown. Results: Their data showed that EGFR-AS1 and ROCK1 were upregulated in ESCC and positively correlated. Survival analysis showed that high EGFR-AS1 and ROCK1 expression levels predicted poor survival. In ESCC cells, EGFR-AS1 overexpression led to upregulated ROCK1, while miR-145 overexpression led to downregulated ROCK1 and reduced effects of EGFR-AS1 overexpression. Bioinformatics analysis showed that miR-145 may bind EGFR-AS1, while overexpression of EGFR-AS1 and miR-145 did not significantly affect each other. In esophageal squamous cell carcinoma (ESCC) cells, EGFR-AS1 and ROCK1 overexpression mediated the increased rates of ECSS cell invasion and migration. Overexpression of miR-145 played an opposite role and attenuated the effects of EGFR-AS1 overexpression. Conclusion: Therefore, EGFR-AS1 may upregulate ROCK1 by sponging miR-145 to promote ESCC cell invasion and migration.
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