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Galectin-9 suppresses the proliferation of gastric cancer cells in vitro
- Source :
- Oncology Reports. 35:851-860
- Publication Year :
- 2015
- Publisher :
- Spandidos Publications, 2015.
-
Abstract
- Gastric cancer is the second-leading cause of cancer-related mortality worldwide, and the prognosis of advanced gastric cancer remains poor. Galectin-9 (Gal-9) is a tandem-repeat-type galectin that has recently been demonstrated to exert anti-proliferative effects on various types of cancer cells. The aim of our present study was to evaluate the effects of Gal-9 on human gastric cancer cells and the expression levels of microRNAs (miRNAs) associated with the antitumor effects of Gal-9 in vitro. In our initial experiments, Gal-9 suppressed the proliferation of gastric cancer cell lines in vitro. Our data further revealed that Gal-9 increased caspase-cleaved keratin 18 (CCK18) levels in gastric cancer cells. Additionally, Gal-9 reduced the phosphorylation of vascular endothelial growth factor receptor-3 (VEGFR-3) and insulin-like growth factor-1 receptor (IGF-1R). Furthermore, miRNA expression levels were markedly altered with Gal-9 treatment in vitro. In conclusion, Gal-9 suppressed the proliferation of human gastric cancer cells by inducing apoptosis. These findings suggest that Gal-9 could be a potential therapeutic target in the treatment of gastric cancer.
- Subjects :
- 0301 basic medicine
Cancer Research
Galectins
Cell
Apoptosis
Enzyme-Linked Immunosorbent Assay
In Vitro Techniques
Biology
Keratin 18
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Stomach Neoplasms
Cell Line, Tumor
medicine
Humans
Cell Proliferation
Oligonucleotide Array Sequence Analysis
Galectin
Oncogene
Cancer
General Medicine
medicine.disease
Molecular medicine
Molecular biology
Vascular endothelial growth factor
030104 developmental biology
medicine.anatomical_structure
Oncology
chemistry
030220 oncology & carcinogenesis
Cancer cell
Cancer research
Subjects
Details
- ISSN :
- 17912431 and 1021335X
- Volume :
- 35
- Database :
- OpenAIRE
- Journal :
- Oncology Reports
- Accession number :
- edsair.doi.dedup.....7ae1777d7e27c5026ed5d840f38ca932
- Full Text :
- https://doi.org/10.3892/or.2015.4452