Tamaki Yudate
Tokyo Medical University
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Featured researches published by Tamaki Yudate.
Tumor Biology | 2011
Yasukazu Sagawa; Atsuya Fujitoh; Hirotaka Nishi; Hiroe Ito; Tamaki Yudate; Keiichi Isaka
AbstractUsing the endometrial cancer cell line EI established in our department, we attempted to establish cisplatin (CDDP)-resistant cell lines by incremental exposure and high concentration exposure methods. Three CDDP-resistant cell lines were isolated, which could be distinguished by morphological differences. 1.Upon acquiring CDDP resistance, the cells tended to become small and grow in a floating state. This tendency was especially marked when using incremental exposure method. Using the incremental exposure method, a cell line obtained by isolating and culturing only adherent cells was designated EICR-Ia, and a cell line established by culturing only floating cells was designated EICR-If. A cell line obtained by the high concentration exposure method was designated EICR-II.2.Upon acquiring CDDP resistance, tumor markers such as TPA and LDH increased, while proliferative capability of the cells was lowered.3.The invasion capability was diminished in EICR-If cells, but was increased in EICR-Ia and EICR-II cells.4.Following exposure to CDDP, the intracellular platinum concentrations were markedly elevated in EI and EICR-If cells, whereas the increase was mild in EICR-Ia and EICR-II cells and the concentration was lower than that in parent EI cells.5.Studies of drug resistance gene expression revealed increased expression of MDR1, GSTπ, and Topo-II in EICR-If cells; increased expression of GSTπ in EICR-II cells; but no expression of any of the genes in EICR-Ia cells.6.Analyses of cancer- and apoptosis-related genes showed increased expressions of Bcl-2, c-Myc, p53, and ICE in EICR-If cells.7.Upon acquiring CDDP resistance, sensitivity to mitomycin and adriamycin decreased, but sensitivity to etoposide and 5-fluorouracil increased. The findings indicate that the mechanisms of CDDP resistance are different in the three cell lines.
Gynecologic and Obstetric Investigation | 2002
Keiichi Isaka; Tomoyoshi Akaeda; Hitoshi Itoh; Kazuhiro Hori; Tamaki Yudate; Junko Nagata; Yasunobu Suzuki; Masaomi Takayama
The evolution of therapy for malignant ovarian germ cell tumors is one of the true success stories in oncology. Treatment outcome has improved greatly thanks to cisplatin-based combination chemotherapy. According to the well-established treatment guidelines for advanced cases, we treated a case of stage IV undifferentiated germ cell tumor in which we were able to preserve the patient’s fertility. We concluded that the PEP regimen is an effective treatment for the patient with metastatic germ cell tumor.
Placenta | 1996
Kenya Shiraishi; Atsuya Fujitoh; Tamaki Yudate; Keiichi Isaka; Masaomi Takayama
Oncology Reports | 2002
Keiichi Isaka; Atsuya Fujito; Yasukazu Sagawa; Tamaki Yudate; Hirotaka Nishi; Hiroe Ito; Masaomi Takayama
Gynecologic and Obstetric Investigation | 2002
Keiichi Isaka; Tomoyoshi Akaeda; Hitoshi Itoh; Kazuhiro Hori; Tamaki Yudate; Junko Nagata; Yasunobu Suzuki; Masaomi Takayama
Placenta | 1997
Yoshichika Suzuki; R. Sugiyama; Hiroe Ito; T. Iwaki; Tamaki Yudate; Keiichi Isaka; Masaomi Takayama
Placenta | 1997
Tamaki Yudate
日本産科婦人科學會雜誌 | 1996
Josie Baral; Yoshichika Suzuki; Tamaki Yudate; Keiichi Isaka; Masaomi Takayama
Placenta | 1996
Keiichi Isaka; Kenya Shiraishi; Tamaki Yudate; Atsuya Fujitoh; Masaomi Takayama
Placenta | 1996
Yoshichika Suzuki; Keiichi Isaka; Tamaki Yudate; Masaomi Takayama