Fluorescent in situ hybridization detection of HER-2/neu gene amplification in rhabdomyosarcoma

被引:21
作者
Mark, HFL
Brown, S
Sun, CL
Samy, M
Afify, A
机构
[1] Rhode Isl Hosp, Lifespan Acad Med Ctr, Dept Pathol, Cytogenet Lab, Providence, RI 02903 USA
[2] Brown Univ, Sch Med, Providence, RI 02912 USA
[3] Washington Univ, Dept Pathol, St Louis, MO 63130 USA
关键词
fluorescent in situ hybridization; HER-2/neu oncogene amplification; rhabdomyosarcoma;
D O I
10.1159/000027997
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Embryonal rhabdomyosarcoma is the most common malignant soft-tissue tumor in childhood, comprising 45-50% of childhood sarcomas, Cytogenetic studies of this tumor are rare, In view of the paucity of cytogenetic data on this cancer and based on the finding of HER-2/neu gene amplification in a number of cancers that was detected mostly using the traditional technique of immunohistochemistry, we decided to conduct a pilot study to investigate whether HER-2/neu gene amplification in this tumor can be detected using the newer technique of fluorescent in situ hybridization (FISH), Archival tissues of rhabdomyosarcoma were retrieved and FISH using an HER-2/neu probe was undertaken on formalin-fixed paraffin-embedded tissue sections using a protocol optimized for our laboratory at Rhode Island Hospital. Out of 9 cases of rhabdomyosarcoma studied to date, 1 case clearly showed HER-2/neu gene amplification. Thus, FISH is a sensitive technique suitable for the detection of oncogene amplification and the delineation of tumor heterogeneity in this tumor. Future experiments utilizing additional specimens from our centers as well as from other laboratories will be needed to extend the finding in the present pilot study.
引用
收藏
页码:59 / 63
页数:5
相关论文
共 32 条
[21]  
MIRANDA RN, 1994, AM J PATHOL, V145, P1
[22]   C-ERBB-2 EXPRESSION AND RESPONSE TO ADJUVANT THERAPY IN WOMEN WITH NODE-POSITIVE EARLY BREAST-CANCER [J].
MUSS, HB ;
THOR, AD ;
BERRY, DA ;
KUTE, T ;
LIU, ET ;
KOERNER, F ;
CIRRINCIONE, CT ;
BUDMAN, DR ;
WOOD, WC ;
BARCOS, M ;
HENDERSON, IC .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (18) :1260-1266
[23]  
Persons DL, 1997, MODERN PATHOL, V10, P720
[24]   CYTOGENETIC ANALYSIS USING QUANTITATIVE, HIGH-SENSITIVITY, FLUORESCENCE HYBRIDIZATION [J].
PINKEL, D ;
STRAUME, T ;
GRAY, JW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (09) :2934-2938
[25]  
PRESS MF, 1993, CANCER RES, V53, P4960
[26]  
Raney Jr RB, 1993, PRINCIPLES PRACTICE, P769
[27]  
REISSMANN PT, 1989, ONCOGENE, V4, P839
[28]   THE NEU ONCOGENE - AN ERB-B-RELATED GENE ENCODING A 185,000-MR TUMOR-ANTIGEN [J].
SCHECHTER, AL ;
STERN, DF ;
VAIDYANATHAN, L ;
DECKER, SJ ;
DREBIN, JA ;
GREENE, MI ;
WEINBERG, RA .
NATURE, 1984, 312 (5994) :513-516
[29]   HUMAN-BREAST CANCER - CORRELATION OF RELAPSE AND SURVIVAL WITH AMPLIFICATION OF THE HER-2 NEU ONCOGENE [J].
SLAMON, DJ ;
CLARK, GM ;
WONG, SG ;
LEVIN, WJ ;
ULLRICH, A ;
MCGUIRE, WL .
SCIENCE, 1987, 235 (4785) :177-182
[30]  
Young SR, 1996, GENE CHROMOSOME CANC, V16, P130, DOI 10.1002/(SICI)1098-2264(199606)16:2<130::AID-GCC7>3.0.CO