Author/Authors :
Barker، نويسنده , , Karen T. and Spendlove، نويسنده , , Hayley E. and Banu، نويسنده , , Nassera S. and Bridge، نويسنده , , Julia A. and Fisher، نويسنده , , Cyril and Shipley، نويسنده , , Janet and Garrett، نويسنده , , Michelle and Manyonda، نويسنده , , Isaac and Houlston، نويسنده , , Richard S.، نويسنده ,
Abstract :
Germline mutations in Fumarate Hydratase (FH) cause the development of leiomyomas and leiomyosarcomas in the syndromes Multiple Cutaneous and Uterine Leiomyomata (MCUL1) and Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC). There is little evidence, however, that FH mutation plays a role in the development of sporadic leiomyomas or leiomyosarcomas. Such observations do not, however, exclude a role for FH in tumour development outside the context of MCUL1/HLRCC, as it is possible that FH expression could be silenced by epigenetic mechanisms. To explore this possibility we have developed a highly specific antibody to FH and analysed a series of forty-five fresh-frozen uterine leiomyomas and nine leiomyosarcomas for FH expression.
Keywords :
fumarate hydratase , Western blotting , Leiomyosarcoma , Leiomyoma