Barker Karen T, Spendlove Hayley E, Banu Nassera S, Bridge Julia A, Fisher Cyril, Shipley Janet, Garrett Michelle, Manyonda Isaac, Houlston Richard S
Section of Cancer Genetics, Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey SM2 5NG, UK.
Cancer Lett. 2006 Apr 8;235(1):136-40. doi: 10.1016/j.canlet.2005.04.017. Epub 2005 Jun 8.
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.
富马酸水合酶(FH)的种系突变会导致多发性皮肤和子宫平滑肌瘤综合征(MCUL1)以及遗传性平滑肌瘤病和肾细胞癌(HLRCC)中平滑肌瘤和平滑肌肉瘤的发生。然而,几乎没有证据表明FH突变在散发性平滑肌瘤或平滑肌肉瘤的发生中起作用。不过,这些观察结果并不排除FH在MCUL1/HLRCC背景之外的肿瘤发生中的作用,因为FH表达有可能通过表观遗传机制被沉默。为了探究这种可能性,我们开发了一种针对FH的高度特异性抗体,并分析了一系列45个新鲜冷冻的子宫平滑肌瘤和9个平滑肌肉瘤中的FH表达情况。