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Characteristic miR-24 Expression in Gastric Cancers among Atomic Bomb Survivors
- Source :
- Pathobiology. 82:68-75
- Publication Year :
- 2015
- Publisher :
- S. Karger AG, 2015.
-
Abstract
- Objective: To elucidate the mechanism of radiation-induced cancers, we analyzed the expression profiles of microRNAs extracted from formalin-fixed paraffin-embedded (FFPE) gastric cancer (GC) tissue samples from atomic bomb survivors. Methods: The expression levels of miR-21, miR-24, miR-34a, miR-106a, miR-143, and miR-145 were measured by quantitative reverse transcription polymerase chain reaction (qRT-PCR). Results: The expression of microRNAs was measured by qRT-PCR in a Hiroshima University Hospital cohort comprising 32 patients in the high-dose-exposed group and 18 patients in the low-dose-exposed group who developed GC after the bombing. The GC cases showing high expression of miR-24, miR-143, and miR-145 were more frequently found in the high-dose-exposed group than in the low-dose-exposed group. We next performed qRT-PCR of miR-24, miR-143, and miR-145 in a cohort from the Hiroshima Red Cross Hospital and Atomic-Bomb Survivors Hospital comprising 122 patients in the high-dose-exposed group and 48 patients in the low-dose-exposed group who developed GC after the bombing. High expressions of miR-24 and miR-143 were more frequently found in the high-dose-exposed group than in the low-dose-exposed group. Multivariate analysis demonstrated that only high expression of miR-24 was an independent predictor for the exposure status. Conclusion: These results suggest that the measurement of miR-24 expression from FFPE samples is useful to identify radiation-associated GC.
- Subjects :
- Oncology
medicine.medical_specialty
Multivariate analysis
business.industry
Cancer
Retrospective cohort study
Cell Biology
General Medicine
University hospital
medicine.disease
Pathology and Forensic Medicine
Reverse transcription polymerase chain reaction
Real-time polymerase chain reaction
Internal medicine
microRNA
Cohort
medicine
business
Molecular Biology
Subjects
Details
- ISSN :
- 14230291 and 10152008
- Volume :
- 82
- Database :
- OpenAIRE
- Journal :
- Pathobiology
- Accession number :
- edsair.doi...........2fd9613b05d519d69814f418e1a07269