Tomoyuki Takei
Gunma University
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Publication
Featured researches published by Tomoyuki Takei.
Journal of Biomedical Science | 2003
Kazuhiro Suzuki; Hiroshi Matsui; Nobuaki Ohtake; Seiji Nakata; Tomoyuki Takei; Haruki Nakazato; Hironobu Okugi; Hidekazu Koike; Yoshihiro Ono; Kazuto Ito; Kohei Kurokawa; Hidetoshi Yamanaka
An association between the Pro/Pro genotype of p53 codon 72 and a lower risk of prostate cancer in Caucasians was recently reported. However, the association of this polymorphism with prostate cancer risk in a Japanese population has not been clarified. We performed a case-control study consisting of 114 prostate cancer patients and 105 noncancer controls. Sixty-nine percent (79 of 114) of the patients had a positive family history. The genotypic frequencies in the controls were 39.0% for Arg/Arg, 54.3% for Arg/Pro and 6.7% for Pro/Pro; they were in Hardy-Weinberg equilibrium. When a comparison of the distribution of the p53 codon 72 polymorphism was made between patients with a first-degree family history and all control subjects, the adjusted odds ratios (ORs) for prostate cancer associated with the Arg/Arg, Arg/Pro and Pro/Pro genotypes were 1.00, 0.99 [95% confidence interval (CI) 0.53-1.88] and 2.80 (95% CI 1.04-7.53), respectively. When stratification of cases was performed based on clinical stage (localized or metastatic cancer) and pathological grade (a Gleason score of <7 or > or =7), there tended to be a greater number of patients with localized cancers among those patients with the Arg/Pro genotype than among those with the Arg/Arg genotype (overall cases: age-adjusted OR 0.36, 95% CI 0.13-1.00, p = 0.049; positive family history cases: age-adjusted OR 0.25, 95% CI 0.075-0.84, p = 0.025). In addition, there tended to be a greater number of patients with low-grade cancers among those with the Pro/Pro genotype than among those with other genotypes (overall cases: age-adjusted OR 0.41, 95% CI 0.13-1.30, p = 0.13; positive family history cases: age-adjusted OR 0.20, 95% CI 0.004-0.89, p = 0.035). The present findings suggest that the Pro/Pro genotype of p53 codon 72 played a role in prostate cancer susceptibility in a Japanese population. However, the Pro allele did not appear to worsen such clinical parameters as clinical stage or pathological grade.
International Journal of Urology | 2003
Kazuhiro Suzuki; Hiroshi Matsui; Nobuaki Ohtake; Seiji Nakata; Tomoyuki Takei; Hidekazu Koike; Haruki Nakazato; Hironobu Okugi; Masaru Hasumi; Yoshitatsu Fukabori; Kohei Kurokawa; Hidetoshi Yamanaka
Aim: Vitamin D acts as an antiproliferative agent against prostate cells. Epidemiological study has shown that a low level of serum vitamin D concentration is a risk factor for prostate cancer. Vitamin D acts via vitamin D receptor (VDR), and an association of genetic polymorphisms of the VDR gene has been reported. In the current study, we examined the association of VDR gene polymorphisms with familial prostate cancer in a Japanese population.
Cancer Letters | 2003
Kazuhiro Suzuki; Hiroshi Matsui; Haruki Nakazato; Hidekazu Koike; Hironobu Okugi; Masaru Hasumi; Nobuaki Ohtake; Seiji Nakata; Tomoyuki Takei; Motoaki Hatori; Kazuto Ito; Hidetoshi Yamanaka
Association between genetic polymorphisms of CYP1A1 and familial prostate cancer risk was examined by a case-control study of 185 individuals. Although the individual analysis of m1 or m2 genotype of CYP1A1 showed no significant association with prostate cancer risk, the presence of any mutated alleles significantly increased prostate cancer risk in comparison with wild-type genotypes by combination analysis (odds ratio [OR]=2.38; 95% confidence interval [CI]=1.72-3.29; P=0.0069). Furthermore, metastatic cancer had a significant association with mutated alleles of m1 and m2. These finding suggested that CYP1A1 polymorphisms has an association with prostate cancer risk, especially with progression of prostate cancer.
International Journal of Urology | 2000
Seiji Nakata; Hirotomo Takahashi; Nobuaki Ohtake; Tomoyuki Takei; Hidetoshi Yamanaka
Background : In North America, the incidence and mortality of prostate cancer has been declining since the early 1990s. We calculated the age‐adjusted death rates, age‐specific death rates and standardized mortality ratio (SMR) for prostate cancer in Japan and analyzed their features.
Anticancer Research | 2003
Haruki Nakazato; Kazuhiro Suzuki; Hiroshi Matsui; Hidekazu Koike; Hironobu Okugi; Nobuaki Ohtake; Tomoyuki Takei; Seiji Nakata; Masaru Hasumi; Kazuto Ito; Kohei Kurokawa; Hidetoshi Yamanaka
Anticancer Research | 2003
Kazuhiro Suzuki; Haruki Nakazato; Hiroshi Matsui; Hidekazu Koike; Hironobu Okugi; Nobuaki Ohtake; Tomoyuki Takei; Seiji Nakata; Masaru Hasumi; Hidetoshi Yamanaka
Anticancer Research | 2003
Hidekazu Koike; Kazuhiro Suzuki; Tetsuo Satoh; Nobuaki Ohtake; Tomoyuki Takei; Seiji Nakata; Hidetoshi Yamanaka
Anticancer Research | 2002
Kazuhiro Suzuki; Nobuaki Ohtake; Seiji Nakata; Tomoyuki Takei; Hiroshi Matsui; Yoshihiro Ono; Haruki Nakazato; Masaru Hasumi; Hidekazu Koike; Kazuto Ito; Yoshitatsu Fukabori; Kohei Kurokawa; Hidetoshi Yamanaka
Nihon Toseki Igakkai Zasshi | 2007
Yoshitaka Sekine; Motoaki Hatori; Tomoyuki Takei; Bunzo Kashiwagi; Tomohiro Magari; Yuji Fukuma; Masahiro Nishii; Tatsuya Hamano; Takumi Yamamoto; Yasuhiro Shibata; Kazuto Ito; Kohei Kurokawa; Masami Machida; Masamichi Hayashi; Kazuhiro Suzuki
The Journal of Urology | 2004
Masaru Hasumi; Kazuhiro Suzuki; Haruki Nakazato; Hiroshi Matsui; Hidekazu Koike; Hironobu Okugi; Bunzo Kashiwagi; Masahiro Nishii; Nobuaki Ohtake; Seiji Nakata; Tomoyuki Takei; Kazuto Ito; Hidetoshi Yamanaka