scholarly journals Hematopoietic pre‐B cell leukemia transcription factor interacting protein is overexpressed in gastric cancer and promotes gastric cancer cell proliferation, migration, and invasion

2015 ◽  
Vol 106 (10) ◽  
pp. 1313-1322 ◽  
Author(s):  
Yingying Feng ◽  
Ling Li ◽  
Xiaomei Zhang ◽  
Yunjing Zhang ◽  
Yingchun Liang ◽  
...  
Keyword(s):  
Gastric Cancer ◽  
Cell Proliferation ◽  
Transcription Factor ◽  
Gastric Cancer Cell ◽  
Migration And Invasion ◽  
Cancer Cell Proliferation ◽  
Cell Leukemia ◽  
Interacting Protein ◽  
B Cell Leukemia ◽  
Gastric Cancer Cell Proliferation

scholarly journals MiR-214 regulate gastric cancer cell proliferation, migration and invasion by targeting PTEN

2013 ◽  
Vol 13 (1) ◽  
pp. 68 ◽  
Author(s):  
Ting-Song Yang ◽  
Xiao-Hu Yang ◽  
Xu-Dong Wang ◽  
Yi-Ling Wang ◽  
Bo Zhou ◽  
...  
Keyword(s):  
Gastric Cancer ◽  
Cell Proliferation ◽  
Cancer Cell ◽  
Gastric Cancer Cell ◽  
Migration And Invasion ◽  
Cancer Cell Proliferation ◽  
Gastric Cancer Cell Proliferation

scholarly journals MicroRNA-103a inhibits gastric cancer cell proliferation, migration and invasion by targeting c-Myb

2014 ◽  
Vol 48 (1) ◽  
pp. 78-85 ◽  
Author(s):  
Jinlong Liang ◽  
Xianfeng Liu ◽  
Hongpeng Xue ◽  
Bing Qiu ◽  
Bin Wei ◽  
...  
Keyword(s):  
Gastric Cancer ◽  
Cell Proliferation ◽  
Cancer Cell ◽  
Gastric Cancer Cell ◽  
Migration And Invasion ◽  
Cancer Cell Proliferation ◽  
Gastric Cancer Cell Proliferation

scholarly journals MiR-450a-5p Inhibits Gastric Cancer Cell Proliferation, Migration, and Invasion and Promotes Apoptosis via Targeting CREB1 and Inhibiting AKT/GSK-3β Signaling Pathway

2021 ◽  
Vol 11 ◽  
Author(s):  
Ya-Jun Zhao ◽  
Jun Zhang ◽  
Yong-Cang Wang ◽  
Liang Wang ◽  
Xin-Yang He
Keyword(s):  
Gastric Cancer ◽  
Cell Proliferation ◽  
Signaling Pathway ◽  
Cancer Cell ◽  
Gastric Cancer Cell ◽  
Luciferase Reporter ◽  
Migration And Invasion ◽  
Cancer Cell Proliferation ◽  
Gastric Cancer Cell Proliferation ◽  
Gsk 3Β

Gastric cancer seriously affects human health and research on gastric cancer is attracting more and more attentions. In recent years, molecular targets have become the research focus. Accumulating evidence indicates that miR-450a-5p plays a critical role in cancer progression. However, the biological role of miR-450a-5p in gastric carcinogenesis remains largely unknown. In this study, we explore the effects and mechanisms of miR-450a-5p on the development and progression of gastric cancer. We used gain-of-function approaches to investigate the role of miR-450a-5p on gastric cancer cell proliferation, migration, invasion, and apoptosis using biological and molecular techniques including real-time quantitative PCR (RT-qPCR), CCK-8, colony formation, flow cytometry, Western blot, wound healing, transwell chamber, dual luciferase reporter, and tumor xenograft mouse model. We found that gastric cancer cells have low expression of miR-450a-5p and overexpression of miR-450a-5p inhibited gastric cancer cell proliferation, migration and invasion, and induced apoptosis in vitro. Moreover, we demonstrated that ectopic expression of miR-450a-5p inhibited gastric cancer growth in vivo. At the molecular level, overexpression of miR-450a-5p significantly increased the expression of pro-apoptotic proteins, including caspase-3, caspase-9, and Bax, and inhibited the expression of anti-apoptotic protein Bcl-2. Luciferase reporter experiment suggested that camp response element binding protein 1 (CREB1) had a negative correlation with miR-450a-5p expression, and knockdown of CREB1 alleviated gastric cancer growth. Furthermore, we also found that miR-450a-5p inhibited the activation of AKT/GSK-3β signaling pathway to inhibit the progression of gastric cancer. Collectively, miR-450a-5p repressed gastric cancer cell proliferation, migration and invasion and induced apoptosis through targeting CREB1 by inhibiting AKT/GSK-3β signaling pathway. MiR-450a-5p could be a novel molecular target for the treatment of gastric cancer.

Sign in / Sign up

Export Citation Format

Share Document