Project/Area Number |
18K19582
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Research Category |
Grant-in-Aid for Challenging Research (Exploratory)
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Allocation Type | Multi-year Fund |
Review Section |
Medium-sized Section 55:Surgery of the organs maintaining homeostasis and related fields
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Research Institution | Hiroshima University |
Principal Investigator |
Okada Morihito 広島大学, 原爆放射線医科学研究所, 教授 (70446045)
|
Project Period (FY) |
2018-06-29 – 2020-03-31
|
Project Status |
Completed (Fiscal Year 2019)
|
Budget Amount *help |
¥6,240,000 (Direct Cost: ¥4,800,000、Indirect Cost: ¥1,440,000)
Fiscal Year 2019: ¥3,120,000 (Direct Cost: ¥2,400,000、Indirect Cost: ¥720,000)
Fiscal Year 2018: ¥3,120,000 (Direct Cost: ¥2,400,000、Indirect Cost: ¥720,000)
|
Keywords | 放射線被曝 / 低線量CT / 染色体異常 / 肺癌 / CT検査 |
Outline of Final Research Achievements |
Because it was difficult to recognize the chromosome which overlapped as two another chromosome by the image recognition software, at first we have set the manufacture condition of the most suitable chromosome specimen. Furthermore, we have established the PNA-FISH method which was observable in the optical microscope using red or green chemical pigments to recognize PNA probe as well as a fluorescent dye.We have developed the automatic analysis software of the chromosome consisting of the centromere and the telomere visualized with red and green pigments by PNA probe, based on the automatic analysis software for the chromosome specimen by the Giemsa's stain. DNA double-strand breaks and chromosome aberrations increased after a single standard-dose chest CT examination, whereas there was no difference in the number of DNA damages observed before and after a single low-dose chest CT examination.
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Academic Significance and Societal Importance of the Research Achievements |
福島原発事故を契機に国民の放射線被曝に関する懸念は一気に高まった。これまでCT検査による放射線被曝の障害に関する科学的データは皆無である。染色体異常の発生頻度は放射線被曝線量と強い相関を示すため、その定量的評価に有用な指標となる。染色体異常の検出を迅速に行うハイスループット染色体解析法を確立した本研究により、個々の患者におけるCT検査の安全性、術後フォローでの頻度、リスク評価スコアリング、抗癌剤の影響、利益/リスク比を示すことができ、肺癌診療のみならず一般の実地診療においても有意義であり、患者や医療従事者の安心に繋がる。
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