YIC-IR
MiR-489 inhibited the development of gastric cancer via regulating HDAC7 and PI3K
其他题名MiR-489 inhibited the development of gastric cancer via regulating HDAC7 and PI3K
Haiyan Zhang1; Lingyun Li2; Cuicui Yuan3; Congcong Wang3; Tiantian Gao3; Zhiwei Zheng1
发表期刊World Journal of Surgical Oncology
ISSN1477-7819
2020
卷号18期号:1
英文摘要Background Mounting evidences have displayed that the dysregulation of miRNAs plays important roles in the pathogenesis of gastric cancer (GC). The purpose of this study was to explore the biological functions and potential mechanism of miR-489 in GC progression. Methods Quantitative real-time PCR (qRT-PCR) and western blot were performed to examine the mRNA expression and protein levels of miR-489 and HDAC7. The relationship between miR-489 and HDAC7 was analyzed by Spearman rank correlation. 3-(4,5-dimethylthiazolyl-2)-2,5-diphenyltetrazolium bromide (MTT) assay and transwell assays were conducted for determining the effect of miR-489 and HDAC7 on GC cell viability, migration, and invasion. TargetScan and luciferase reporter assay were used to confirm the target gene of miR-489 in GC cells. Results The findings showed that miR-489 was dramatically decreased in GC tissues and GC cell lines (SGC-7901 and MKN45). Moreover, it was closely correlated with overall survival (OS) and progression-free survival (PFS) of GC patients. Downregulation of miR-489 significantly promoted GC cell proliferation, invasion, and migration. Additionally, HDAC7 was confirmed as the direct target of miR-489. Knockdown of HDAC7 exerted inhibited effect on GC progression and it markedly overturned miR-489 inhibitor-medicated effect on GC cells. More interestingly, via targeting HDAC7, miR-489 blocked the activation of PI3K Conclusions Correctively, miR-489 played as a tumor suppressor in GC cell growth by targeting HDAC7, and miR-489 might function as a novel biomarker for diagnosis or therapeutic targets of human GC.
中文摘要Background Mounting evidences have displayed that the dysregulation of miRNAs plays important roles in the pathogenesis of gastric cancer (GC). The purpose of this study was to explore the biological functions and potential mechanism of miR-489 in GC progression. Methods Quantitative real-time PCR (qRT-PCR) and western blot were performed to examine the mRNA expression and protein levels of miR-489 and HDAC7. The relationship between miR-489 and HDAC7 was analyzed by Spearman rank correlation. 3-(4,5-dimethylthiazolyl-2)-2,5-diphenyltetrazolium bromide (MTT) assay and transwell assays were conducted for determining the effect of miR-489 and HDAC7 on GC cell viability, migration, and invasion. TargetScan and luciferase reporter assay were used to confirm the target gene of miR-489 in GC cells. Results The findings showed that miR-489 was dramatically decreased in GC tissues and GC cell lines (SGC-7901 and MKN45). Moreover, it was closely correlated with overall survival (OS) and progression-free survival (PFS) of GC patients. Downregulation of miR-489 significantly promoted GC cell proliferation, invasion, and migration. Additionally, HDAC7 was confirmed as the direct target of miR-489. Knockdown of HDAC7 exerted inhibited effect on GC progression and it markedly overturned miR-489 inhibitor-medicated effect on GC cells. More interestingly, via targeting HDAC7, miR-489 blocked the activation of PI3K Conclusions Correctively, miR-489 played as a tumor suppressor in GC cell growth by targeting HDAC7, and miR-489 might function as a novel biomarker for diagnosis or therapeutic targets of human GC.
语种英语
文献类型期刊论文
条目标识符http://ir.yic.ac.cn/handle/133337/34499
专题中国科学院烟台海岸带研究所
作者单位1.People’s Hospital of Rizhao
2.Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences
3.The People’s Hospital of zhangqiu area
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GB/T 7714
Haiyan Zhang,Lingyun Li,Cuicui Yuan,et al. MiR-489 inhibited the development of gastric cancer via regulating HDAC7 and PI3K[J]. World Journal of Surgical Oncology,2020,18(1).
APA Haiyan Zhang,Lingyun Li,Cuicui Yuan,Congcong Wang,Tiantian Gao,&Zhiwei Zheng.(2020).MiR-489 inhibited the development of gastric cancer via regulating HDAC7 and PI3K.World Journal of Surgical Oncology,18(1).
MLA Haiyan Zhang,et al."MiR-489 inhibited the development of gastric cancer via regulating HDAC7 and PI3K".World Journal of Surgical Oncology 18.1(2020).
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