2017 Fiscal Year Final Research Report
Clinical application to significance and growth control of the chromosome instability in carcinogenesis, the progress of gastrointestinal cancer
Project/Area Number |
15K10127
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Digestive surgery
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Research Institution | Kyushu University (2016-2017) National Hospital Organization, Kyushu Cancer Center (2015) |
Principal Investigator |
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Co-Investigator(Kenkyū-buntansha) |
江頭 明典 独立行政法人国立病院機構別府医療センター(臨床研究部), 臨床研究部, その他 (00419524)
藤 也寸志 独立行政法人国立病院機構(九州がんセンター臨床研究センター), その他部局等, 院長 (20217459)
森田 勝 独立行政法人国立病院機構(九州がんセンター臨床研究センター), その他部局等, その他 (30294937)
沖 英次 九州大学, 大学病院, 助教 (70380392)
佐伯 浩司 九州大学, 大学病院, 助教 (80325448)
|
Project Period (FY) |
2015-04-01 – 2018-03-31
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Keywords | 食道癌 / メチル化 / FANCJ |
Outline of Final Research Achievements |
In multiple esophageal cancer and multiple Lugol-voiding lesion of esophagus, the LINE-1 methylation in the esophageal nomal mucosa significantly decreased. We suggest that the genome-wide hypomethylation was wide participated in outbreak of many carcinogenesis. In addition, methylation abnormality of various chemokines and in cancer of the esophagus was associated with genome-wide hypomethylation. An effect of the preoperation chemotherapy (5FU+CDDP) was high in esophageal cancer that had a low FANCJ expression, and the group that enforced 5FU+CDDP after surgery in a low FANCJ expression had a better prognosis than surgery alone group. Furthermore, in the patients of esophageal cancer that gave chemotherapy after surgery, the low FANCJ expression group significantly had a better prognosis than overexpression group. The expression of FANCJ can become a useful marker as effect measurement of the chemotherapy.
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Free Research Field |
総合生物
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