Abstract | BACKGROUND: Overexpression of G-protein coupled receptor 34 (GPR34) affects the progression and prognosis of human gastric adenocarcinoma, however, the role of GPR34 in gastric cancer development and progression has not been well-determined. The current study aimed to investigate the effect of GPR34 knockdown on the proliferation, migration, and apoptosis of HGC-27 gastric cancer cells and the underlying mechanisms. METHODS: The expression of GPR34 in gastric cancer cell line HGC-27 was detected by quantitative real-time reverse transcription-polymerase chain reaction (RT-PCR) and Western blotting. HGC-27 cells were employed to construct the stable GPR34 knockdown cell model in this study. Real-time RT-PCR and Western blotting were applied to validate the effect of short hairpin RNA ( ShRNA) on the expression of GPR34 in HGC-27 gastric cells. The proliferation, migration of these cells were examined by Cell Counting Kit-8 and transwell. We also measured expression profile of PI3K/PDK1/AKT and ERK using Western blotting. RESULTS: The ShRNA directed against GPR34 effectively inhibited both endogenous mRNA and protein expression levels of GPR34, and significantly down-regulated the expression of PIK3CB (P < 0.01), PIK3CD (P < 0.01), PDK1 (P < 0.01), phosphorylation of PDK1 (P < 0.01), Akt (P < 0.01), and ERK (P < 0.01). Furthermore, GPR34 knockdown resulted in an obvious reduction in HGC-27 cancer cell proliferation and migration activity (P < 0.01). CONCLUSIONS:
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Authors | Zhong-Tian Jin, Kun Li, Mei Li, Zhi-Gang Ren, Fu-Shun Wang, Ji-Ye Zhu, Xi-Sheng Leng, Wei-Dong Yu |
Journal | Chinese medical journal
(Chin Med J (Engl))
Vol. 128
Issue 4
Pg. 545-9
(Feb 20 2015)
ISSN: 2542-5641 [Electronic] China |
PMID | 25673461
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- G-protein-coupled receptor 34
- RNA, Small Interfering
- Receptors, Lysophospholipid
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Topics |
- Apoptosis
(genetics, physiology)
- Blotting, Western
- Cell Line, Tumor
- Cell Proliferation
(genetics, physiology)
- Humans
- RNA, Small Interfering
(genetics)
- Real-Time Polymerase Chain Reaction
- Receptors, Lysophospholipid
(genetics, metabolism)
- Stomach Neoplasms
(genetics, metabolism)
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