HER-2/neu (c-erb-B2) gene and protein in breast cancer

被引:0
作者
Ross, JS
Fletcher, JA
机构
[1] Albany Med Coll, Dept Pathol & Lab Med, Albany, NY 12208 USA
[2] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
关键词
breast neoplasms; HER-2/neu; prognosis; proto-oncogene c-erb-B2; therapy;
D O I
暂无
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The HER-2/neu oncogene encodes a transmembrane tyrosine kinase receptor with extensive homology to the epidermal growth factor receptor. The association of HER-2/neu gene and protein abnormalities with prognosis in breast cancer is presented by considering a series of 52 published studies including more than 16,000 patients. The relative advantages and disadvantages of Southern blot testing, polymerase chain reaction amplification, and fluorescence in situ hybridization assays designed to detect HER-2/neu gene amplification are compared with HER-2/neu protein overexpression assays performed with immunohistochemical techniques applied to frozen and paraffin-embedded tissues and enzyme immunoassays performed on tumor cytosols. The importance of HER-2/neu protein overexpression in ductal carcinoma in situ, and HER-2/neu protein status in uncommon breast diseases in female patients and breast cancer in male patients are also considered. The potential value of HER-2/neu protein status for the prediction of response to therapy in breast cancer is presented for standard hormonal therapy, cytotoxic chemotherapy, and radiation therapy. Also evaluated is the status of serum-based testing for circulating HER-2/neu receptor protein and its ability to predict disease outcome and therapy response. Finally, preliminary data concerning use of antibody-based therapies directed against HER-2/neu protein and their potential use in breast cancer treatment are considered.
引用
收藏
页码:S53 / S67
页数:15
相关论文
共 164 条
[1]   Biophenotypes of breast carcinoma in situ defined by image analysis of biological parameters [J].
Albonico, G ;
Querzoli, P ;
Ferretti, S ;
Magri, E ;
Nenci, I .
PATHOLOGY RESEARCH AND PRACTICE, 1996, 192 (02) :117-123
[2]   AMPLIFICATION OF C-ERBB-2 AND AGGRESSIVE HUMAN-BREAST TUMORS [J].
ALI, IU ;
CAMPBELL, G ;
LIDEREAU, R ;
CALLAHAN, R .
SCIENCE, 1988, 240 (4860) :1795-1796
[3]  
ALLAN SM, 1994, CELL BIOPHYS, V24-5, P93, DOI 10.1007/BF02789219
[4]  
Allred DC, 1998, MODERN PATHOL, V11, P155
[5]   HER-2/NEU IN NODE-NEGATIVE BREAST-CANCER - PROGNOSTIC-SIGNIFICANCE OF OVEREXPRESSION INFLUENCED BY THE PRESENCE OF INSITU CARCINOMA [J].
ALLRED, DC ;
CLARK, GM ;
TANDON, AK ;
MOLINA, R ;
TORMEY, DC ;
OSBORNE, CK ;
GILCHRIST, KW ;
MANSOUR, EG ;
ABELOFF, M ;
EUDEY, L ;
MCGUIRE, WL .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (04) :599-605
[6]   OVEREXPRESSION OF HER-2 NEU AND ITS RELATIONSHIP WITH OTHER PROGNOSTIC FACTORS CHANGE DURING THE PROGRESSION OF INSITU TO INVASIVE BREAST-CANCER [J].
ALLRED, DC ;
CLARK, GM ;
MOLINA, R ;
TANDON, AK ;
SCHNITT, SJ ;
GILCHRIST, KW ;
OSBORNE, CK ;
TORMEY, DC ;
MCGUIRE, WL .
HUMAN PATHOLOGY, 1992, 23 (09) :974-979
[7]   DETECTION OF C-ERBB-2 RELATED PROTEIN IN SERA FROM BREAST-CANCER PATIENTS - RELATIONSHIP TO ERBB2 GENE AMPLIFICATION AND C-ERBB-2 PROTEIN OVEREXPRESSION IN TUMOR [J].
ANDERSEN, TI ;
PAUS, E ;
NESLAND, JM ;
MCKENZIE, SJ ;
BORRESEN, AL .
ACTA ONCOLOGICA, 1995, 34 (04) :499-504
[8]   neu/erbB-2 amplification identifies a poor-prognosis group of women with node-negative breast cancer [J].
Andrulis, IL ;
Bull, SB ;
Blackstein, ME ;
Sutherland, D ;
Mak, C ;
Sidlofsky, S ;
Pritzker, KPH ;
Hartwick, RW ;
Hanna, W ;
Lickley, L ;
Wilkinson, R ;
Qizilbash, A ;
Ambus, U ;
Lipa, M ;
Weizel, H ;
Katz, A ;
Baida, M ;
Mariz, S ;
Stoik, G ;
Dacamara, P ;
Strongitharm, D ;
Geddie, W ;
McCready, D .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (04) :1340-1349
[9]   EXPRESSION OF RAS P21, P53 AND C-ERBB-2 IN ADVANCED BREAST-CANCER AND RESPONSE TO FIRST LINE HORMONAL-THERAPY [J].
ARCHER, SG ;
ELIOPOULOS, A ;
SPANDIDOS, D ;
BARNES, D ;
ELLIS, IO ;
BLAMEY, RW ;
NICHOLSON, RI ;
ROBERTSON, JFR .
BRITISH JOURNAL OF CANCER, 1995, 72 (05) :1259-1266
[10]  
BABIAK J, 1992, CANCER, V70, P770, DOI 10.1002/1097-0142(19920815)70:4<770::AID-CNCR2820700409>3.0.CO