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Takuji Tanaka

Researcher at Gifu University

Publications -  15
Citations -  1490

Takuji Tanaka is an academic researcher from Gifu University. The author has contributed to research in topics: Azoxymethane & Hesperidin. The author has an hindex of 13, co-authored 15 publications receiving 1467 citations.

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Journal Article

Chemoprevention of Spontaneous Endometrial Cancer in Female Donryu Rats by Dietary Indole-3-carbinol

TL;DR: It is suggested that dietary I3C inhibits spontaneous occurrence of endometrial adenocarcinoma as well as preneoplastic lesions in Donryu rats and may be due to its induction of estradiol 2-hydroxylation.
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Chemoprevention of mouse urinary bladder carcinogenesis by the naturally occurring carotenoid astaxanthin

TL;DR: AX is a possible chemopreventive agent for bladder carcinogenesis and such an effect of AX may be partly due to suppression of cell proliferation, as indicated by results of mice treated with AX or CX.
Journal Article

Chemoprevention of 4-Nitroquinoline 1-Oxide-induced Oral Carcinogenesis by Dietary Curcumin and Hesperidin: Comparison with the Protective Effect of β-Carotene

TL;DR: The modifying effects of two natural products, curcumin and hesperidin, given during the initiation and postinitiation phases of oral carcinogenesis initiated with 4-nitroquinoline 1-oxide (4-NQO) were investigated in male F344 rats and compared with that of beta-carotene as discussed by the authors.
Journal Article

Chemoprevention of Rat Oral Carcinogenesis by Naturally Occurring Xanthophylls, Astaxanthin and Canthaxanthin

TL;DR: The results indicate that AX and CX are possible chemopreventers for oral carcinogenesis, and such effects may be partly due to suppression of cell proliferation.
Journal Article

Chemoprevention of diethylnitrosamine-induced hepatocarcinogenesis by a simple phenolic acid protocatechuic acid in rats

TL;DR: Although the precise mechanisms of PCA-induced inhibition of hepatocarcinogenesis remain to be elucidate, it is likely that the inhibitory effects during the initiation and postinitiation phases may be due to alteration in hepatic ornithine decarboxylase activity under the present experimental condition.