Few FH mutations in sporadic counterparts of tumor types observed in hereditary leiomyomatosis and renal cell cancer families.

نویسندگان

  • Maija Kiuru
  • Rainer Lehtonen
  • Johanna Arola
  • Reijo Salovaara
  • Heikki Järvinen
  • Kristiina Aittomäki
  • Jari Sjöberg
  • Tapio Visakorpi
  • Sakari Knuutila
  • Jorma Isola
  • Brett Delahunt
  • Riitta Herva
  • Virpi Launonen
  • Auli Karhu
  • Lauri A Aaltonen
چکیده

Loss of function mutations in the fumarate hydratase (fumarase, FH) gene were recently identified as the cause for dominantly inherited uterine and cutaneous leiomyomas and renal cell cancer. To further evaluate the role of FH in tumorigenesis, we screened FH mutations from tumor types seen in hereditary leiomyomatosis and renal cell cancer mutation carriers-41 uterine and 10 cutaneous leiomyomas, 52 renal cell carcinomas, 53 sarcomas, 29 prostate carcinomas, and 15 lobular breast carcinomas. Few mutations were detected. Biallelic inactivation of FH was found in one uterine leiomyosarcoma, one cutaneous leiomyoma, and one soft tissue sarcoma. Whereas the two former lesions were shown to originate from a germ-line mutation, the soft tissue sarcoma is to our knowledge the first example of purely somatic inactivation of FH in tumors.

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عنوان ژورنال:
  • Cancer research

دوره 62 16  شماره 

صفحات  -

تاریخ انتشار 2002