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[Hemangioblastoma and von Hippel-Lindau Disease].
Takayanagi, Shunsaku; Takami, Hirokazu; Tanaka, Shota; Saito, Nobuhito.
Afiliação
  • Takayanagi S; Department of Neurosurgery, the University of Tokyo.
No Shinkei Geka ; 50(1): 101-110, 2022 Jan.
Article em Ja | MEDLINE | ID: mdl-35169090
Hemangioblastoma(HB)is a tumor that frequently occurs in von Hippel-Lindau(VHL)disease, a hereditary tumor disease. It is a benign tumor and excision is the first choice of treatment, but in VHL disease, where HB occurs frequently, the emergence of more promising molecularly-targeted therapeutic agents has been desired. In this paper, we first explain HB and VHL disease and then outline the function of the VHL gene and the mechanism of onset of VHL disease. After that, we explain the analysis technology and frequency of VHL gene abnormalities and finally describe HIF2α inhibitors, which are promising as molecularly-targeted therapeutic agents for VHL disease. As the medical system for personalized medicine/precision medicine is being developed in Japan, it is expected that HB and VHL diseases will attract attention as target diseases in the future.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hemangioblastoma / Doença de von Hippel-Lindau Limite: Humans País/Região como assunto: Asia Idioma: Ja Revista: No Shinkei Geka Ano de publicação: 2022 Tipo de documento: Article País de publicação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hemangioblastoma / Doença de von Hippel-Lindau Limite: Humans País/Região como assunto: Asia Idioma: Ja Revista: No Shinkei Geka Ano de publicação: 2022 Tipo de documento: Article País de publicação: Japão