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MiR-28-5p targeting GAGE12I inhibits gastric cancer cell proliferation, migration and invasion in vitro
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Li-ping XIAO1, Qing-fang ZENG2, Tao ZHAN3
Chinese Journal of Clinical Pharmacology | 2025, 41(6) : 790 - 793
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Chinese Journal of Clinical Pharmacology | 2025, 41(6): 790-793
Clinical and Basic Bridging Research
MiR-28-5p targeting GAGE12I inhibits gastric cancer cell proliferation, migration and invasion in vitro
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Li-ping XIAO1, Qing-fang ZENG2, Tao ZHAN3
Affiliations
  • 1.Oncology Department, Ganzhou People’s Hospital/Southern Hospital Ganzhou Hospital, Ganzhou 341000, Jiangxi Province, China
  • 2.Oncdogy Department, Ganzhou Cancer Hospital, Ganzhou 341000, Jiangxi Province, China
  • 3.Department of Oncology, Jingdezhen First People’s Hospital, Jingdezhen 351000, Jiangxi Province, China
Published: 2025-03-28 doi: 10.13699/j.cnki.1001-6821.2025.06.008
Outline
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Objective

To investigate the in vitro inhibitory effects of microRNA-28-5p (miR-28-5p) targeting G antigen 12I antibody (GAGE12I) on the proliferation, migration, and invasion of gastric cancer cells.

Methods

SGC-7901 cell were randomly divided into miR-28-5p group (miR-28-5p mimic), miR-NC group (miR-28-5p negative control mimic), shGAGE12I group (GAGE12I knockout) and blank group (GAGE12I not knockout). Cell proliferation, migration, and invasion capabilities were evaluated using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) colorimetric assay and invasion chambers. Bioinformatics analysis and luciferase activity assays were conducted to examine the interaction between miR-28-5p and GAGE12I.

Results

The proliferation rates of miR-28-5p and miR-NC groups were (99.90±10.30)% and (48.25±4.15)%; the invasion rates were (145.57±14.52)% and (67.30±6.95)%; the mobility rates were (103.58±10.75)% and (43.18±4.26)%, respectively, the differences were statistically significant (all P<0.05). The proliferation rates of shGAGE12I group and blank group were (99.80±10.20)% and (35.50±3.58)%; the invasion rates were (142.70±13.65)% and (65.30±6.75)%; the mobility rates were (103.55±10.06)% and (48.38±4.52)%, respectively, the differences were statistically significant (all P<0.05). GAGE12I was the target of miR-28-5p.

Conclusion

MiR-28-5p negatively regulates GAGE12I and reduces the proliferation, invasion and migration of gastric cancer cells.

G antigen 12I antibody  /  microRNAs-28-5p  /  gastric cancer  /  proliferation  /  migration  /  invasion studies
Li-ping XIAO, Qing-fang ZENG, Tao ZHAN. MiR-28-5p targeting GAGE12I inhibits gastric cancer cell proliferation, migration and invasion in vitro[J]. Chinese Journal of Clinical Pharmacology, 2025 , 41 (6) : 790 -793 . DOI: 10.13699/j.cnki.1001-6821.2025.06.008
Year 2025 volume 41 Issue 6
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doi: 10.13699/j.cnki.1001-6821.2025.06.008
  • Receive Date:2024-08-15
  • Online Date:2026-08-04
  • Published:2025-03-28
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History
  • Received:2024-08-15
Funding
Affiliations
    1.Oncology Department, Ganzhou People’s Hospital/Southern Hospital Ganzhou Hospital, Ganzhou 341000, Jiangxi Province, China
    2.Oncdogy Department, Ganzhou Cancer Hospital, Ganzhou 341000, Jiangxi Province, China
    3.Department of Oncology, Jingdezhen First People’s Hospital, Jingdezhen 351000, Jiangxi Province, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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