shiwata I
Jikei University School of Medicine
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Publication
Featured researches published by shiwata I.
Human Cell | 2008
Isamu Ishiwata; Chieko Ishiwata; Masayuki Soma; Megumi Iguchi; Kazushige Kiguchi; Tomoharu Tamagawa; Ishiwata I; Hiroshi Ishikawa
A cell line designated HTMMT was established from the human uterine carcinosarcoma (composed of leiomyosarcoma and adenocarcinoma) of a 66-year-old Japanese woman. The cell line grew well and 83 serial passages were successively done within 24 months. The cell line contained spindle- or fibrous-shaped cells that revealed neoplastic and pleomorphic features, and multipled rapidly without contact inhibition. These cells were characterized as possessing myofibrils. The karyotype exhibited hyperploidy and the chromosome number was ranged from 87 to 100. The cells were transplanted into an immune-depressed hamster cheek pouch or into nude mouse skin, but produced no tumors. We supported the combination theory for the histogenesis of the carcinosarcoma.
Human Cell | 2007
Ishiwata I; Makoto Yasuda; Takashi Hirano; Hiroshi Ishikawa
A cell line designated “HEPFT” was established from a human fallopian tubal hepatoid carcinoma. This line grew well without interruption for 13 months and was subcultivated over 35 times. The cells were spherical and polygonal in shape and showed neoplastic and pleomorphic features such as a bizarre aggregation of chromatin granules, an irregular thickening membrane and multiple large nucleoli. The cells formed epithelial colonies with ajigsaw puzzle-like arrangement and multilayering without contact inhibition. The cells contained moderate to abundant amounts of eosinophilic cytoplasm and were immunohistochemically positive for α-fetoprotein. The cells proliferated rapidly, and the population doubling time was about 45 h. The chromosome number showed a wide distribution of aneuploidy. The modal chromosome number was stable in the hyper triploid range and many marker chromosomes were observed. The culture cells produced bile and a large amount of lentil lectin-reactive α-fetoprotein. The recently developed bacterial artificial chromosome array comparative genomic hybridization facilitated detailed analysis with high resolution and sensitivity. Different profiles of genomic copy-number abnormalities were demonstrated in various chromosomal regions in HEPFT cells.
Human Cell | 2008
Ishiwata I; Emiko Ishiwata; Takashi Hirano
Two human malignant mesothelioma cell lines, which we designated “epithelial mesothelioma cells” and “fibrous mesothelioma cells”, were established from the pleural fluid containing malignant mesothelial cells of a 72-year-old Japanese man. These cell lines were separated by the colonial techniques from the initiation of the primary cultures and grew well without interruption for 12 years. They were characterized as producing hyaluronic acid. These cell lines displayed different biological characteristics, including morphology, heterotransplantability and genetics using with BAC array CGH. The epithelial mesothelioma cells were epithelial in shape and transplantable into the subcutis of nude mice, while the cells of the fibrous mesothelioma line were fibroblast-like and transplantable into the submucosa of Hamster’s cheek pouches but not into the subcutis of nude mice. The mesotheliomas are classified into three types: epithelial mesothelioma, fibrous mesothelioma and mixed type. The gene copy number losses observed on 9p21.3, 9p21.2, 9p21.1, among others maybe a major mechanism of malignant mesothelioma carcinogenesis. We considered and supported the combination theory for the histogenesis of malignant mesothelioma.
Human Cell | 2008
Isamu Ishiwata; Yuko Tokieda; Megumi Iguchi; Tomoharu Tamagawa; Chieko Ishiwata; Ishiwata I; Kazushige Kiguchi; Hiroshi Ishikawa
The cell line designated HHUS was established from human uterine cervical keratinizing squamous cell carcinoma. The HHUS cell line was subcultivated more than 70 times within 3 years. The cultured cells. polygonal or spindle, with neoplastic and pleomorphic feature. apprared epithelial in shape, with a pavement-like arrangement and grew in multi-layers without contact inhibition. The chromosome number was varied from 40 to 88. and the modal number was stable in diploid range. The cultured cells produced keratinizing squamous cell carcinomas by heterotransplantation into the subcutis of nude mice. The HHUS cells were characterized as producing large amounts of SCC, in vitro and possessing HPV-59 DNA genomes.
Human Cell | 2000
Ishiwata I; Yuko Tokieda; Kiguchi K; Kahei Sato; Hiroshi Ishikawa
Human Cell | 2001
Ishiwata I; Tokeida Y; Megumi Iguchi; Chieko Ishiwata; Kiguchi K; Yasumoto S; Kahei Sato; Toshiaki Tachibana; Hisashi Hashimoto; Hiroshi Ishikawa
Human Cell | 1999
Ishiwata I; Sudo T; Kiguchi K; Hiroshi Ishikawa
Human Cell | 2001
Kahei Sato; Koji Hosaka; Ohkawa M; Yuko Tokieda; Ishiwata I
Human Cell | 1997
Ishiwata I; Yuko Tokieda; Chieko Ishiwata; Okane N; Megumi Iguchi; Kahei Sato; Hiroshi Ishikawa
Human Cell | 1999
Kiguchi K; Ishiwata I; Yuko Tokieda; Megumi Iguchi; Chieko Ishiwata; Hiroshi Ishikawa