Amplification of erbB-4 oncogene occurs less frequently than that of erbB-2 in primary human breast cancer

被引:39
作者
Vogt, U
Bielawski, K
Schlotter, CM
Bosse, U
Falkiewicz, B
Podhajska, AJ
机构
[1] European Lab Assoc, Sect Ibbenburen, D-49477 Ibbenburen, Germany
[2] Univ Gdansk, Fac Biotechnol, Mol Diagnost Div, PL-80822 Gdansk, Poland
[3] Med Univ Gdansk, PL-80822 Gdansk, Poland
[4] European Lab Assoc, Sect Gdansk, PL-80822 Gdansk, Poland
[5] Infect Dis Hosp, PL-80214 Gdansk, Poland
[6] St Elisabeth Hosp, Dept Obstet Gynecol, D-49477 Ibbenburen, Germany
[7] Inst Pathol, D-49090 Osnabruck, Germany
[8] Univ Gdansk, Fac Chem, PL-80952 Gdansk, Poland
关键词
epidermal growth factor receptor family; tyrosine kinase receptors; double differential PCR; erb;
D O I
10.1016/S0378-1119(98)00454-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
ErbB-4 protein is a recently discovered member of the ErbB family. The role of ErbB-4 protein in mammary-gland tissue has not been definitively established. To date, the expression of erbB-4 in breast tissue has been determined in only a few cases and, to the best of our knowledge, its amplification has not been examined. We therefore used the double differential polymerase chain reaction (ddPCR) for determination of the amplification profile of erbB-4 and erbB-2, another gene from the ErbB family, in human primary breast cancer specimens. We examined the amplification of the genes in 20 normal breasts and 176 invasive breast cancer samples. Amplification of erbB-2 was detected in 19% and erbB-4 in 13% of the samples studied. Go-amplification of the two oncogenes was found in only five out of 176 samples. Human breast cancer-derived cell lines in most cases overexpress both erbB-2 and erbB-4 (Beerli et al., 1995. Mol. Cell Biol. 15, 6496-6505; Han et al., 1995. Proc. Natl. Acad. Sci. USA 92, 9747-9751), but data on separate erbB-2 overexpression, without overexpression of erbB-4, were also reported (Wosikowski et al., 1997. Clin. Cancer Res. 3, 2405-2414). At the gene level, we found that co-amplification of the genes in the case of human breast cancer is rare. Moreover, an inverse association of the erbB-4 amplification with estrogen receptor activity and direct correlation with the tumor size were found. Due to these correlations, erbB-4 oncogene amplification can be assumed to be of prognostic or predictive value in the diagnosis of breast cancer. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:375 / 380
页数:6
相关论文
共 30 条
[21]  
Lyne JC, 1997, CANCER J SCI AM, V3, P21
[22]  
Marengo SR, 1997, MOL CARCINOGEN, V19, P165
[23]   LIGAND-SPECIFIC ACTIVATION OF HER4/P180(ERBB4), A 4TH MEMBER OF THE EPIDERMAL GROWTH-FACTOR RECEPTOR FAMILY [J].
PLOWMAN, GD ;
CULOUSCOU, JM ;
WHITNEY, GS ;
GREEN, JM ;
CARLTON, GW ;
FOY, L ;
NEUBAUER, MG ;
SHOYAB, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (05) :1746-1750
[24]   THE C-ERBB-2 PROTOONCOGENE AS A PROGNOSTIC AND PREDICTIVE MARKER IN BREAST-CANCER - A PARADIGM FOR THE DEVELOPMENT OF OTHER MACROMOLECULAR MARKERS - A REVIEW [J].
RAVDIN, PM ;
CHAMNESS, GC .
GENE, 1995, 159 (01) :19-27
[25]   ERBB2 oncogene in human breast cancer and its clinical significance [J].
Révillion, F ;
Bonneterre, J ;
Peyrat, JP .
EUROPEAN JOURNAL OF CANCER, 1998, 34 (06) :791-808
[26]   A tyrosine kinase profile of prostate carcinoma [J].
Robinson, D ;
He, F ;
Pretlow, T ;
Kung, HJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (12) :5958-5962
[27]  
SPIESSL B, 1990, TNM ATLAS, P173
[28]  
WAINSTEIN MA, 1994, CANCER RES, V54, P6049
[29]  
Wosikowski K, 1997, CLIN CANCER RES, V3, P2405
[30]  
ZIMONJIC DB, 1995, ONCOGENE, V10, P1235