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Ameloblastoma cell lines derived from different subtypes demonstrate distinct developmental patterns in a novel animal experimental model
FUCHIGAMI, Takao; SUZUKI, Hajime; YOSHIMURA, Takuya; KIBE, Toshiro; CHAIRANI, Elissa; KIYONO, Tohru; KISHIDA, Michiko; KISHIDA, Shosei; NAKAMURA, Norifumi.
  • FUCHIGAMI, Takao; Kagoshima University. School of Medical and Dental Sciences. Department of Oral and Maxillofacial Surgery. Kagoshima. JP
  • SUZUKI, Hajime; Kagoshima University. School of Medical and Dental Sciences. Department of Oral and Maxillofacial Surgery. Kagoshima. JP
  • YOSHIMURA, Takuya; Kagoshima University. School of Medical and Dental Sciences. Department of Oral and Maxillofacial Surgery. Kagoshima. JP
  • KIBE, Toshiro; Kagoshima University. School of Medical and Dental Sciences. Department of Oral and Maxillofacial Surgery. Kagoshima. JP
  • CHAIRANI, Elissa; Kagoshima University. School of Medical and Dental Sciences. Department of Oral and Maxillofacial Surgery. Kagoshima. JP
  • KIYONO, Tohru; National Cancer Center Research Institute. Tokyo. JP
  • KISHIDA, Michiko; Kagoshima University. School of Medical and Dental Sciences. Department of Biochemistry and Genetics. Kagoshima. JP
  • KISHIDA, Shosei; Kagoshima University. School of Medical and Dental Sciences. Department of Biochemistry and Genetics. Kagoshima. JP
  • NAKAMURA, Norifumi; Kagoshima University. School of Medical and Dental Sciences. Department of Oral and Maxillofacial Surgery. Kagoshima. JP
J. appl. oral sci ; 28: e20190558, 2020. graf
Article in English | LILACS, BBO | ID: biblio-1101249
ABSTRACT
Abstract Objective Ameloblastoma is a representative odontogenic tumor comprising several characteristic invasive forms, and its pathophysiology has not been sufficiently elucidated. A stable animal experimental model using immortalized cell lines is crucial to explain the factors causing differences among the subtypes of ameloblastoma, but this model has not yet been disclosed. In this study, a novel animal experimental model has been established, using immortalized human ameloblastoma-derived cell lines. Methodology Ameloblastoma cells suspended in Matrigel were subcutaneously transplanted into the heads of immunodeficient mice. Two immortalized human ameloblastoma cell lines were used AM-1 cells derived from the plexiform type and AM-3 cells derived from the follicular type. The tissues were evaluated histologically 30, 60, and 90 days after transplantation. Results Tumor masses formed in all transplanted mice. In addition, the tumors formed in each group transplanted with different ameloblastoma cells were histologically distinct the tumors in the group transplanted with AM-1 cells were similar to the plexiform type, and those in the group transplanted with AM-3-cells were similar to the follicular type. Conclusions A novel, stable animal experimental model of ameloblastoma was established using two cell lines derived from different subtypes of the tumor. This model can help clarify its pathophysiology and hasten the development of new ameloblastoma treatment strategies.
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Full text: Available Index: LILACS (Americas) Main subject: Ameloblastoma / Disease Models, Animal / Neoplasms, Experimental Type of study: Prognostic study Limits: Animals Language: English Journal: J. appl. oral sci Journal subject: Dentistry Year: 2020 Type: Article Affiliation country: Japan Institution/Affiliation country: Kagoshima University/JP / National Cancer Center Research Institute/JP

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Full text: Available Index: LILACS (Americas) Main subject: Ameloblastoma / Disease Models, Animal / Neoplasms, Experimental Type of study: Prognostic study Limits: Animals Language: English Journal: J. appl. oral sci Journal subject: Dentistry Year: 2020 Type: Article Affiliation country: Japan Institution/Affiliation country: Kagoshima University/JP / National Cancer Center Research Institute/JP