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High expression of RELM-α correlates with poor prognosis and promotes angiogenesis in gastric cancer
- Source :
- Oncology Reports
- Publication Year :
- 2015
- Publisher :
- Spandidos Publications, 2015.
-
Abstract
- Accumulating evidence indicates that resistin-like molecule-α (RELM-α) is involved in angiogenesis, while the clinical significance and the exact role of RELM-α in gastric cancer remain obscure. The aim of the present study was to evaluate the clinical significance of RELM-α in gastric cancer, and to investigate its effective mechanisms in order to identify a potential therapeutic target. The expression levels of RELM-α in 92 gastric cancer and adjacent normal tissues were investigated and the relationship between RELM-α expression and the clinicopathological characteristics was explored. To investigate the potential role of RELM-α in gastric cancer cell biological behavior, the cell proliferation, migration and invasion assays were conducted using two gastric cancer cell lines (SGC7901 and MKN45). We also assessed whether RELM-α gene silencing modulates angiogenesis using small interference RNA in cancer cell lines, and investigated its effect on nuclear factor (NF)-κB activation and vascular endothelial growth factor (VEGF) and MMP-9 expression. Contrasting sharply with the strong RELM-α-positive tumors, adjacent normal tissues and cell lines exhibited negative or weakly positive expression (P
- Subjects :
- Vascular Endothelial Growth Factor A
Cancer Research
Angiogenesis
Cell
Biology
chemistry.chemical_compound
Stomach Neoplasms
Cell Line, Tumor
Biomarkers, Tumor
medicine
Humans
Gene silencing
Neoplasm Invasiveness
Cell Proliferation
Neovascularization, Pathologic
Oncogene
NF-kappa B
Cancer
General Medicine
Cell cycle
medicine.disease
Gene Expression Regulation, Neoplastic
Vascular endothelial growth factor
medicine.anatomical_structure
Matrix Metalloproteinase 9
Oncology
chemistry
Cancer cell
Cancer research
Intercellular Signaling Peptides and Proteins
Corrigendum
Subjects
Details
- ISSN :
- 17912431 and 1021335X
- Volume :
- 34
- Database :
- OpenAIRE
- Journal :
- Oncology Reports
- Accession number :
- edsair.doi.dedup.....e5e12465e721e36214f324a0a55264f4
- Full Text :
- https://doi.org/10.3892/or.2015.3943