Mechanisms of hormone independence in human breast cancer

被引:0
作者
Murphy, LC [1 ]
机构
[1] Univ Manitoba, Dept Biochem & Mol Biol, Winnipeg, MB R3E 0W3, Canada
来源
IN VIVO | 1998年 / 12卷 / 01期
关键词
breast cancer; estrogen; antiestrogen; endocrine resistance;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The progression of human breast cancer from a hormone dependent to a hormone independent phenotype is a clinical problem which limits the long term usefulness of the relatively nontoxic endrocrine therapies. It is also associated with a more aggressive form of the disease. Since expression of estrogen receptor-alpha appears to be relatively stable phenotype during breast cancer progression, the majority of breast tumors that develop hormone independence and resistance to endocrine therapies do so despite the continued expression of estrogen receptor-alpha. Several possible mechanisms that may contribute to the progression of breast cancer from hormone dependence to independence, either alone or in combination with other mechanisms, are reviewed. These include variant or mutated estrogen receptor-alpha, ligant independent activation of estrogen receptor-alpha, altered expression of down-stream estrogen target genes, post receptor and pharmacological alterations.
引用
收藏
页码:95 / 106
页数:12
相关论文
共 165 条
[1]  
AGTHOVEN TV, 1992, CANCER RES, V52, P5082
[2]   AIB1, a steroid receptor coactivator amplified in breast and ovarian cancer [J].
Anzick, SL ;
Kononen, J ;
Walker, RL ;
Azorsa, DO ;
Tanner, MM ;
Guan, XY ;
Sauter, G ;
Kallioniemi, OP ;
Trent, JM ;
Meltzer, PS .
SCIENCE, 1997, 277 (5328) :965-968
[3]   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
[4]   STIMULATION OF ESTROGEN RECEPTOR-MEDIATED TRANSCRIPTION AND ALTERATION IN THE PHOSPHORYLATION STATE OF THE RAT UTERINE ESTROGEN-RECEPTOR BY ESTROGEN, CYCLIC ADENOSINE-MONOPHOSPHATE, AND INSULIN-LIKE GROWTH FACTOR-I [J].
ARONICA, SM ;
KATZENELLENBOGEN, BS .
MOLECULAR ENDOCRINOLOGY, 1993, 7 (06) :743-752
[5]  
ARTEAGA CL, 1993, CELL GROWTH DIFFER, V4, P193
[7]  
BASSET P, 1994, CANCER-AM CANCER SOC, V74, P1045, DOI 10.1002/1097-0142(19940801)74:3+<1045::AID-CNCR2820741511>3.0.CO
[8]  
2-7
[9]   EXPRESSION OF TRANSFORMING GROWTH FACTOR-ALPHA AND ITS MESSENGER RIBONUCLEIC-ACID IN HUMAN-BREAST CANCER - ITS REGULATION BY ESTROGEN AND ITS POSSIBLE FUNCTIONAL-SIGNIFICANCE [J].
BATES, SE ;
DAVIDSON, NE ;
VALVERIUS, EM ;
FRETER, CE ;
DICKSON, RB ;
TAM, JP ;
KUDLOW, JE ;
LIPPMAN, ME ;
SALOMON, DS .
MOLECULAR ENDOCRINOLOGY, 1988, 2 (06) :543-555
[10]   THE PROGESTERONE ANTAGONIST RU486 ACQUIRES AGONIST ACTIVITY UPON STIMULATION OF CAMP SIGNALING PATHWAYS [J].
BECK, CA ;
WEIGEL, NL ;
MOYER, ML ;
NORDEEN, SK ;
EDWARDS, DP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (10) :4441-4445