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Upregulated INHBA expression is associated with poor survival in gastric cancer
- Source :
- Medical Oncology. 29:77-83
- Publication Year :
- 2010
- Publisher :
- Springer Science and Business Media LLC, 2010.
-
Abstract
- Expression microarrays are widely used for investigating the candidate molecular targets in human cancer. While genome-wide expression signatures screened by gene set enrichment analysis (GSEA) were not performed in Chinese gastric cancer (GC). To gain new molecular targets for GC, GSEA analysis was performed. In the present study, GSEA were used to pick out differentially expressed gene sets of our database. Total RNA of paired tissue samples (n = 48) and a tissue microarray containing 132 paired tissues were used to further validate expression levels of INHBA and its correction with clinicopathological factors. Upregulated INHBA expression in gastric cancer was screened and further confirmed by qPCR and immunostaining analysis. Increased INHBA expression was significantly correlated with the diameter of cancer and depth of tumor invasion. Patients with higher expression levels of INHBA had a shorter disease-free survival rate. It was effective to gain new molecular targets for GC by GSEA analysis. INHBA may be a poor survival indicator of GC.
- Subjects :
- Male
Cancer Research
Microarray
Kaplan-Meier Estimate
Biology
Real-Time Polymerase Chain Reaction
Disease-Free Survival
Stomach Neoplasms
Gene expression
Biomarkers, Tumor
medicine
Humans
Survival rate
Aged
Inhibin-beta Subunits
Neoplasm Staging
Oligonucleotide Array Sequence Analysis
Tissue microarray
Reverse Transcriptase Polymerase Chain Reaction
Gene Expression Profiling
Cancer
Hematology
General Medicine
Middle Aged
Prognosis
medicine.disease
Immunohistochemistry
Molecular biology
Gene expression profiling
Real-time polymerase chain reaction
Oncology
Tissue Array Analysis
Female
DNA microarray
Genome-Wide Association Study
Subjects
Details
- ISSN :
- 1559131X and 13570560
- Volume :
- 29
- Database :
- OpenAIRE
- Journal :
- Medical Oncology
- Accession number :
- edsair.doi.dedup.....19306ce0acf531d59430a31ff656da61
- Full Text :
- https://doi.org/10.1007/s12032-010-9766-y