The research on chemoprevention and therapy for oral cancer by selective inhibitors of cyclooxygenase-2
| Project/Area Number |
12671957
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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 |
Surgical dentistry
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| Research Institution | Department of Oral and Maxillofacial Surgery |
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Principal Investigator |
YAMAMOTO Kazuhiko Nara Medical University, Oral and Maxillofacial Surgery, Assistant Professor, 医学部, 講師 (20243842)
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| Co-Investigator(Kenkyū-buntansha) |
DENDA Ayumi Nara Medical University, Oncological Pathology, Assistant Professor, 医学部, 講師 (90110858)
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| Project Period (FY) |
2000 – 2001
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| Project Status |
Completed (Fiscal Year 2001)
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| Budget Amount *help |
¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 2001: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 2000: ¥1,900,000 (Direct Cost: ¥1,900,000)
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| Keywords | oral cancer / cyclooxygenase-2 / 4-nitroquinoline 1-oxide / nimesulide / etodolac / chemoprevention / rat |
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| Research Abstract |
The expression of cyclooxygenase (COX)-2 is elevated in various cancer and considered to be related to carcinogen sis. We analyzed the expression of COX-2 protein in the tongue lesions induced by 4-nitroquinoline 1-oxide (4-NQO) in rats and the inhibitory efficacy of selective inhibitors, nimesulide (NIM) and etodolac. The lesions induced by 4-NQO are classified into hyperplasias, dysphasias, papillomas and squamous cell carcinomas (SCCs). The immunohistochemical expression of COX-2 protein is elevated especially in dysplasias and carcinomas. Western blot analysis showed 6-fold increase of COX-2 protein level in SCCs compared with normal epithelium. The administration of NIM and etodolac after initiation phase by 4-NQO decreased the incidences and multiplicities of SCCs dose-dependently. But, the incidences of dysphasia's, putative preneoplastic lesions, did not decreased. Then, we analyzed the effect of NIM and etodolac in the initiation phase of tongue carcinogensis by 4-NQO. The incidence of dysphasia's decreased dose-dependently. From the results described above, in rat tongue carcinogen sis, COX-2 protein level increases in dysphasia's and SCCs, and NIM and etodolac inhibit the development of dysphasia's and the progression to SCCs. Therefore, selective COX-2 inhibitors can be chemo preventive medicines for human oral cancer.
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Report
(3 results)
Research Products
(4 results)
