Enhanced expression of the UROC28 gene in human breast cancer: Relationship to ERBB2 gene expression

被引:0
作者
Kamagata, C [1 ]
Tsuji, N [1 ]
Kondoh, K [1 ]
Sasaki, M [1 ]
Kobayashi, D [1 ]
Yagihashi, A [1 ]
Watanabe, N [1 ]
机构
[1] Sapporo Med Univ, Dept Lab Diag & Clin Lab Med, Sch Med, Chuo Ku, Sapporo, Hokkaido 0608543, Japan
关键词
breast cancer; diagnostic marker; ERBB2; estradiol; molecular targets; UROC28;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: ERBB2, a highly important oncogene in invasive breast cancer, is not only a prognostic factor but also a predictive marker for response to therapeutic agents. Recently, An et al. (10) identified a novel gene, UROC28, that is also overexpressed in breast cancer. To examine possible interrelationships, we quantitated UROC28 and ERBB2 mRNA in breast cancers. Materials and Methods: The expression of UROC28 and ERBB2 mRNA in breast cancer tissues were determined using RT-PCR. The expression was also examined in T-47D breast cancer cells treated with estrogen. Results: UROC28 mRNA expression was greater in cancers than in noncancerous tissues (p<0.0001), as was ERBB2 mRNA. ERBB2 and UROC28 gene expression was dose-dependently down-regulated in T-47D breast cancer cells treated with estradiol. However UROC28 mRNA and ERBB2 mRNA expression did not correlate with one another. Conclusion: These results indicate that UROC28 may be a useful target molecule in breast cancer diagnosis and treatment, complementing ERBB2.
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页码:4087 / 4091
页数:5
相关论文
共 29 条
[1]  
ADNANE J, 1989, ONCOGENE, V4, P1389
[2]  
An G, 2000, CANCER RES, V60, P7014
[3]   An intron 1 enhancer element mediates oestrogen-induced suppression of ERBB2 expression [J].
Bates, NP ;
Hurst, HC .
ONCOGENE, 1997, 15 (04) :473-481
[4]   ONCOGENE AMPLIFICATION AND PROGNOSIS IN BREAST-CANCER - RELATIONSHIP WITH SYSTEMIC TREATMENT [J].
BERNS, EMJJ ;
FOEKENS, JA ;
VANSTAVEREN, IL ;
VANPUTTEN, WLJ ;
DEKONING, HYWCM ;
PORTENGEN, H ;
KLIJN, JGM .
GENE, 1995, 159 (01) :11-18
[5]   ERBB2 AMPLIFICATION IS ASSOCIATED WITH TAMOXIFEN RESISTANCE IN STEROID-RECEPTOR POSITIVE BREAST-CANCER [J].
BORG, A ;
BALDETORP, B ;
FERNO, M ;
KILLANDER, D ;
OLSSON, H ;
RYDEN, S ;
SIGURDSSON, H .
CANCER LETTERS, 1994, 81 (02) :137-144
[6]  
BORG A, 1990, CANCER RES, V50, P4332
[7]   HUMANIZATION OF AN ANTI-P185HER2 ANTIBODY FOR HUMAN CANCER-THERAPY [J].
CARTER, P ;
PRESTA, L ;
GORMAN, CM ;
RIDGWAY, JBB ;
HENNER, D ;
WONG, WLT ;
ROWLAND, AM ;
KOTTS, C ;
CARVER, ME ;
SHEPARD, HM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (10) :4285-4289
[8]   DOWN REGULATION OF C-MYC, C-FOS AND ERB-B DURING ESTROGEN-INDUCED PROLIFERATION OF THE CHICK OVIDUCT [J].
COHRS, RJ ;
GOSWAMI, BB ;
SHARMA, OK .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 150 (01) :82-88
[9]  
DATI C, 1990, ONCOGENE, V5, P1001
[10]   Adjuvant chemotherapy plus tamoxifen compared with tamoxifen alone for postmenopausal breast cancer: Meta-analysis of quality-adjusted survival [J].
Gelber, RD ;
Cole, BF ;
Goldhirsch, A ;
Rose, C ;
Fisher, B ;
Osborne, CK ;
Boccardo, F ;
Gray, R ;
Gordon, NH ;
Bengtsson, NO ;
Sevelda, P .
LANCET, 1996, 347 (9008) :1066-1071