Project/Area Number |
16406005
|
Research Category |
Grant-in-Aid for Scientific Research (B)
|
Allocation Type | Single-year Grants |
Section | 海外学術 |
Research Field |
General anatomy (including Histology/Embryology)
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Research Institution | Nagasaki University |
Principal Investigator |
KOJI Takehiko Nagasaki University, Graduate School of Biomedical Sciences, Professor, 大学院医歯薬学総合研究科, 教授 (30170179)
|
Co-Investigator(Kenkyū-buntansha) |
HISHIKAWA Yoshitaka Nagasaki University, Graduate School of Biomedical Sciences, Associate Professor, 大学院医歯薬学総合研究科, 助教授 (60304276)
AN Sucai Nagasaki University, Graduate School of Biomedical Sciences, Instructor, 大学院医歯薬学総合研究科, 助手 (30404213)
IZUMI Shinichi Nagasaki University, Graduate School of Biomedical Sciences, Instructor, 大学院医歯薬学総合研究科, 助手 (40264246)
OKADA Shigeru Okayama University, Graduate School of Medicine and Dentistry and Pharmaceutical Sciences, Professor, Emeritus, 大学院医歯薬学総合研究科, 名誉教授 (20033201)
江島 邦彰 長崎大学, 大学院・医歯薬学総合研究科, 客員研究員 (30309984)
白鳥 康史 岡山大学, 大学院・医歯薬学総合研究科, 教授 (70196624)
|
Project Period (FY) |
2004 – 2006
|
Project Status |
Completed (Fiscal Year 2006)
|
Budget Amount *help |
¥13,100,000 (Direct Cost: ¥13,100,000)
Fiscal Year 2006: ¥3,700,000 (Direct Cost: ¥3,700,000)
Fiscal Year 2005: ¥4,000,000 (Direct Cost: ¥4,000,000)
Fiscal Year 2004: ¥5,400,000 (Direct Cost: ¥5,400,000)
|
Keywords | Myanmar / hepatocellular carcinoma / iron / iron-responsive element binding proteins / hepatitis viruses / apoptosis / electroporation / molecular histochemistry / KGF / 鉄反応エレメント結合蛋白 / 分子組織細胞化学 |
Research Abstract |
The precocious development of hepatocellular carcinoma (HCC) is an emergent problem in Myanmar. As a possible cause, iron overtaken from the environment is implicated. In the present study, we investigated deposition of iron in the HCC tissues and its correlation with cell proliferation and cell death. To collect the tissue samples, we cooperated with Department of Medical Research (DMR/Lower Myanmar). During the research term, we visited Yangon 3 times (December 23-28, 2004, December 15-20, 2005 and February 19-23, 2007) and newly obtained 37 specimens of HCV positive cases. In our visit, we held not only meetings with DMR and Medical University scientists, but also wet-lab courses on various histochemical techniques in which totally 84 medical researchers took part with a good reputation. In addition, we established the Agreement of Academic Cooperation between DMR/Lower Myanmar, Department of Medical Sciences, Ministry of Health and Nagasaki University on February 20, 2007 to promot
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e our collaboration. When 27 specimens of the newly obtained HCC tissues were examined for iron deposition, a significant deposition of iron in Myanmar HCC was found, not like that of Japanese patients. Moreover, we found that the cases with iron deposition had significantly higher Ki-67 labeling indices. Although we found Fas-Fas ligand related TUNEL positive cells in some H CC specimens, the frequency was not correlated significantly with iron deposition. Further, when we investigated liver regeneration after partial hepatectomy in iron-overloaded rat model, the peak of DNA synthesis was put forward significantly and the onset of DNA synthesis was associated temporarily with the expression of KGF and KGFR in hepatocytes. Also, we found the similar phenomena in CC14 treated iron-overloaded rats. These results strongly indicate that accelerated proliferation of hepatocytes by overloaded iron may promote the development of HCC under the conditions to induce hepatocyte proliferation such as viral infection. Less
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