| Project/Area Number |
11670210
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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 |
Experimental pathology
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| Research Institution | GIFU UNIVERSITY |
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Principal Investigator |
YOSHIMI Naoki GIFU UNIVERSITY, SCH.MED.ASSOC.PROFESSOR, 医学部, 助教授 (30166996)
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| Co-Investigator(Kenkyū-buntansha) |
YAMADA Yosuhiro GIFU UNIVERSITY, SCH.MED.ASSOCIATE, 医学部, 助手 (70313872)
MORI Hideki GIFU UNIVERSITY, SCH.MED.PROFESSOR, 医学部, 教授 (70021433)
原 明 岐阜大学, 医学部, 助手 (10242728)
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| Project Period (FY) |
1999 – 2000
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| Project Status |
Completed (Fiscal Year 2000)
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| Budget Amount *help |
¥3,200,000 (Direct Cost: ¥3,200,000)
Fiscal Year 2000: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 1999: ¥1,900,000 (Direct Cost: ¥1,900,000)
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| Keywords | CHEMICALLLY-INDUCED COLON CARCINOGENESIS / B-CATENIN / PRENEOPLASTICLESIONS / RAT / GENEMUTATION / βカテニン / 大腸発癌 |
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| Research Abstract |
Activating mutations in the β-catenin gene is thought to be responsible for the excessive β-catenin signaling involved in the majority of carcinogen-induced colonic carcinomas. To determine if β-catenin signaling is involved in the initial stage of colon carcinogenesis, mutational analysis of the gene and immunohistochemistry for β-catenin protein were performed in the early appearing lesions, including aberrant crypt foci (ACF), of colonic mucosa in rats given azoxymethane (AOM). Male F344 rats received s.c. injections of AOM at a dose of 15 mg/kg body weight, once weekly for 3 weeks and sacrificed 10 weeks after the carcinogen treatment. The colonic mucosa was examined in en face preparations and in serial sections after the observation in whole mount preparations. Microscopical observations in the cross sections have shown two populations of histologically altered crypts. The first type had a macroscopic feature resembling ACF (histologically altered crypts with ACF appearance ; HACA). The second type of altered crypts did not have the ACF-like appearance and could not be clearly distinguished from adjacent normal crypts in whole mount preparations (histologically altered crypts with macroscopically normal-like appearance ; HACN). The β-catenin gene mutations were recognized in 10 out of 15 HACN (67%) and 3 of 15 HACA (20%). Frequent immunoreactivity of β-catenin protein was seen in the cytoplasm of HACN (13 out of 15 cases), whereas apparent accumulation was not confirmed in any HACA analyzed. These results suggest that i) there are two types of putative preneoplastic lesions in cancer-predisposed colonic mucosa and β-catenin signaling may contribute to the initial stage of colon carcinogenesis, ii) HACN are more likely to be direct precursors of colon tumors than HACA in the rat colon carcinogenesis.
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