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Ras gene activation in human small intestinal tumors
D Spandidos1, T Liloglou, D Arvanitis
1UNIV CRETE,SCH MED,IRAKLION,GREECE. AGHIA SOPHIA CHILDRENS HOSP,ATHENS,GREECE. AIR FORCES GEN & VA HOSP,ATHENS,GREECE.
International Journal of Oncology
|May 17, 2011
Summary
Ras p21 oncoprotein was elevated in most small intestinal tumors. H-ras gene mutations were detected for the first time in these tumors, suggesting a role in pathogenesis.
Area of Science:
- Oncology
- Molecular Biology
- Gastroenterology
Background:
- The ras oncoprotein plays a role in cell signaling and cancer development.
- Investigating ras p21 expression and mutations in small intestinal tumors is crucial for understanding their pathogenesis.
Purpose of the Study:
- To investigate the expression of ras p21 oncoprotein in human small intestinal tumors.
- To detect H-ras and K-ras mutations in codon 12 and 13 in these tumors.
- To explore the potential role of ras p21 and H-ras mutations as molecular markers in small intestinal tumors.
Main Methods:
- Immunohistochemical technique using monoclonal antibody Y13-259 to analyze ras p21 levels.
- Polymerase chain reaction (PCR) to detect H-ras and K-ras mutations.
- Comparison of protein levels and mutation status between tumor tissues and adjacent normal tissues.
Main Results:
- Elevated ras p21 oncoprotein levels were observed in 9 out of 13 small intestinal tumors compared to normal tissue.
- H-ras gene mutations in codon 12 were identified in 4 out of 13 tumors, including a Brunner's gland adenoma, lymphoma, leiomyosarcoma, and metastatic adenocarcinoma.
- No K-ras mutations were found in codons 12 or 13.
- This study represents the first demonstration of ras mutations in small intestinal tumors.
Conclusions:
- Ras p21 oncoprotein may be involved in the pathogenesis of small intestinal tumors.
- H-ras mutations are present in a subset of small intestinal tumors.
- Ras p21 oncoprotein and H-ras mutations may serve as molecular genetic markers for small intestinal tumors.
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