| Project/Area Number |
14571750
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Morphological basic dentistry
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| Research Institution | Showa University |
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Principal Investigator |
KOHNO Yohko Showa University, School of Dentistry, Associate Professor, 歯学部, 助教授 (40195681)
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| Co-Investigator(Kenkyū-buntansha) |
TACHIKAWA Thtsuhiko Showa University, School of Dentistry, Professor, 歯学部, 教授 (10085772)
戸野 佳世子 昭和大学, 歯学部, 助手 (60327939)
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| Project Period (FY) |
2002 – 2004
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| Project Status |
Completed (Fiscal Year 2004)
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| Budget Amount *help |
¥2,500,000 (Direct Cost: ¥2,500,000)
Fiscal Year 2004: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 2003: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 2002: ¥800,000 (Direct Cost: ¥800,000)
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| Keywords | Cell cycle / Cyclin G2 / Cyclin G1 / Control factor |
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| Research Abstract |
We have shown that human cyclin G2 is down-regulated in laser capture microdissection using microarray. Western analysis showed detectable cyclin G2 protein in normal but not in malignant oral keratinocyte cell lines. Immunohistochemistry analysis done on oral mucosa, dysplastic oral epithelia and oral cancer epithelia. Cyclin G2 expressed in 100% of normal oral mucosa, 69.1% of dysplastic oral epithelia in the nuclei and 11.1% of oral cancer epithelia in the nuclei. In vitro functional study by ectopic restoration of Cyclin G2 expression in the human malignant squamous cell carcinoma line resulted in a inhibition of cellular proliferation and colony formation with increased population of G1 phase and decreased in S phase. Stable down-regulation of Cyclin G2 by short interference RNA-based gene silencing in immortalized normal oral keratinocytes resulted in enhanced cell growth with increase in S and prominently in G2 phase. Cyclin G2, has been implicated as a negative regulator in cell cycle progression.
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