EXPRESSION OF MEMBERS OF THE MYF GENE FAMILY IN HUMAN RHABDOMYOSARCOMAS

被引:34
|
作者
CLARK, J
ROCQUES, PJ
BRAUN, T
BOBER, E
ARNOLD, HH
FISHER, C
FLETCHER, C
BROWN, K
GUSTERSON, BA
CARTER, RL
COOPER, CS
机构
[1] INST CANC RES,HADDOW LABS,15 COTSWOLD RD,SUTTON SM2 5NG,SURREY,ENGLAND
[2] UNIV HAMBURG,SCH MED,DEPT TOXICOL,W-2000 HAMBURG 13,GERMANY
[3] ROYAL MARSDEN HOSP,DEPT HISTOPATHOL,LONDON SW3 6JJ,ENGLAND
[4] ST THOMAS HOSP,DEPT HISTOPATHOL,LONDON SE1,ENGLAND
[5] UNIV BRISTOL,DEPT PATHOL & MICROBIOL,BRISTOL BS8 1TD,AVON,ENGLAND
基金
英国医学研究理事会;
关键词
D O I
10.1038/bjc.1991.461
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Northern analysis of tumour RNA has been used to examine the expression of members of the myf family of muscle determining genes (myf3, myf4, myf5 and myf6) in a series of 20 rhabdomyosarcomas. A 2.0 kb myf3 transcript was observed in 85% of tumours, a 1.8 kb myf4 transcript was detected in 70% of tumours and a 1.7 kb myf5 transcript was observed in 55% of tumours. Transcription of myf6 occurred in 28% of tumours, but there were several transcript sizes (1.2, 1.5, 2.0 and 3.5 kb) and in some individual tumours two or more transcripts were observed. Only two rhabdomyosarcomas, one classified as embryonal and one as pleomorphic, failed to exhibit transcription of members of the myf gene family. We were unable to detect transcription of myf genes in neuroblastomas, Wilms' tumours, hepatoblastomas, paediatric non-Hodgkin's lymphoma and leiomyosarcomas. When considered together these observations suggest that expression of myf genes could provide an extremely useful marker in the diagnosis of rhabdomyosarcoma.
引用
收藏
页码:1039 / 1042
页数:4
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