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Possible chemoresistance-related genes for gastric cancer detected by cDNA microarray
Kazuhiro Suganuma1, Tetsuro Kubota, Yoshiro Saikawa
1Department of Surgery, School of Medicine, Keio University, Sinjuku-ku, Tokyo 160-8582, Japan. tkubota@sc.itc.keio.ac.jp
Abstract:
To identify chemoresistance-related genes of gastric cancer, we utilized cDNA microarray technology. Thirty-five gastric cancer specimens surgically resected at our institute between 1998 and 1999 were studied for quantification of expression of 6300 genes by means of oligonucleotide microarray methods, and the results were evaluated in comparison with the chemoresistance of the specimens, which was determined by MTT (tetrazolium-based 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay. Inhibition rates (IR) were determined for cisplatin (DDP), 5-fluorouracil (5-FU), mitomycin C or doxorubicin. IR of 60% or more was regarded as sensitive to each agent, and IR of less than 40% was defined as resistant. Clustering was successfully completed for DDP, resulting in selection of 23 candidates as DDP-resistance-related genes, including vascular permeability factor, 2 membrane transporting subunits, and retinoblastoma-binding protein-1. In addition, further selection of DDP-resistance-related genes was performed according to these criteria: 1) Expression of the gene can be detected in more than 70% of resistant tumors. 2) Expression can be detected in less than 30% of sensitive tumors. 3) Expression in tumors is more than twice that of normal mucosa in more than 50% of specimens. Then, metallothionein-IG and heparin-binding epidermal growth factor-like growth factor (HB-EGF) were identified as candidate DDP-resistance-related genes. When known DDP-resistance-related genes were analyzed according to the MTT assay result, families of glutathione-S-transferase and cyclooxygenase-2 genes were also evaluated as resistance-related genes. For 5-FU resistance, dihydropyrimidine dehydrogenase and HB-EGF-like growth factor genes were also suggested to be resistance-related genes. The present study demonstrated that oligonucleotide microarrays can provide information regarding chemoresistance factors in cancer.
Insights
This study used microarray technology to identify genes linked to gastric cancer chemoresistance, discovering potential biomarkers like HB-EGF for cisplatin and 5-FU resistance.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Gastric cancer exhibits significant chemoresistance, necessitating identification of related genes.
- Understanding chemoresistance mechanisms is crucial for improving treatment efficacy.
Purpose of the Study:
- To identify genes associated with chemoresistance in gastric cancer using cDNA microarray.
- To evaluate gene expression patterns in relation to sensitivity and resistance to common chemotherapeutic agents.
Main Methods:
- Oligonucleotide microarray analysis of 6300 genes in 35 gastric cancer specimens.
- Chemoresistance determination using MTT assay for cisplatin (DDP), 5-fluorouracil (5-FU), mitomycin C, and doxorubicin.
- Gene expression analysis and selection based on differential expression in resistant versus sensitive tumors and normal mucosa.
Main Results:
- Identified 23 candidate DDP-resistance-related genes, including vascular permeability factor and retinoblastoma-binding protein-1.
- Metallothionein-IG and heparin-binding epidermal growth factor-like growth factor (HB-EGF) were selected as candidate DDP-resistance genes.
- Glutathione-S-transferase and cyclooxygenase-2 families, dihydropyrimidine dehydrogenase, and HB-EGF were implicated in DDP and 5-FU resistance.
Conclusions:
- Oligonucleotide microarrays are effective for identifying chemoresistance factors in gastric cancer.
- Specific genes like HB-EGF show potential as biomarkers for predicting response to chemotherapy.
- Further validation of identified genes is warranted for clinical application.