Aromatase expression in the human breast

被引:34
作者
Brodie, A [1 ]
Long, B [1 ]
Lu, Q [1 ]
机构
[1] Univ Maryland, Sch Med, Greenebaum Canc Ctr, Dept Pharmacol & Expt Therapeut, Baltimore, MD 21201 USA
关键词
aromatase; breast cancer; normal breast immunocytochemistry;
D O I
10.1023/A:1006029612990
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The plasma levels of free estradiol are very low in postmenopausal women. However, concentrations of estrogens within breast tissue have been reported to be higher than in plasma and similar to plasma concentrations in premenopausal women. One mechanism by which this map occur is for breast cells to synthesize estrogens themselves and produce high concentrations locally. Thus, tumor aromatase may be a significant source of estrogen which stimulates tumor growth. To address the question of the importance of this pathway, we have investigated the expression of aromatase within the normal breast and breast cancers. Because conventional biochemical assays for measuring aromatase activity require relatively large amounts of tissue, we developed an immunocytochemical method using a monoclonal antibody to determine the expression of aromatase. The method can be applied to sections of tumors embedded in paraffin blocks as routinely prepared for pathology, Since we have previously shown that mRNA for aromatase (P450 arom) and the protein are expressed in the same cells of the human placenta, we used in situ hybridization of sequence specific probes to P450 arom mRNA in breast tissue as one method to verify the specificity of the immunocytochemical detection of the enzyme. Both immunocytochemistry and in situ hybridization identified aromatase enzyme and mRNA expression in the epithelial cells of the terminal ductal lobula units (TDLU) and surrounding stromal cells of the normal human breast, and in the tumor epithelial cells and stromal cells of breast cancers. In addition, evidence for the functional significance of tumor aromatase was indicated by a correlation between aromatase activity and expression of proliferating cell nuclear antigen (PCNA) in the tumor, and by increased thymidine into DNA in response to testosterone in tumors in histoculture which had high aromatase activity but not in those with low activity. The findings suggests that estrogen produced locally is important in enhancing proliferation of the tumor.
引用
收藏
页码:S85 / S91
页数:7
相关论文
共 24 条
[1]  
BANKS P, 1989, 71 ANN M END SOC SEA
[2]   EFFECT OF AN AROMATASE INHIBITOR, 4-HYDROXY-4-ANDROSTENE-3,17-DIONE, ON ESTROGEN-DEPENDENT PROCESSES IN REPRODUCTION AND BREAST-CANCER [J].
BRODIE, AMH ;
SCHWARZEL, WC ;
SHAIKH, AA ;
BRODIE, HJ .
ENDOCRINOLOGY, 1977, 100 (06) :1684-1695
[3]  
ESTEBAN JM, 1992, AM J PATHOL, V140, P337
[4]   PROLIFERATING CELL NUCLEAR ANTIGEN (PCNA) IMMUNOLOCALIZATION IN PARAFFIN SECTIONS - AN INDEX OF CELL-PROLIFERATION WITH EVIDENCE OF DEREGULATED EXPRESSION IN SOME NEOPLASMS [J].
HALL, PA ;
LEVISON, DA ;
WOODS, AL ;
YU, CCW ;
KELLOCK, DB ;
WATKINS, JA ;
BARNES, DM ;
GILLETT, CE ;
CAMPLEJOHN, R ;
DOVER, R ;
WASEEM, NH ;
LANE, DP .
JOURNAL OF PATHOLOGY, 1990, 162 (04) :285-294
[5]   PLASMA PRECURSORS OF ESTROGEN .2. CORRELATION OF EXTENT OF CONVERSION OF PLASMA ANDROSTENEDIONE TO ESTRONE WITH AGE [J].
HEMSELL, DL ;
GRODIN, JM ;
BRENNER, PF ;
SIITERI, PK ;
MACDONALD, PC .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1974, 38 (03) :476-479
[6]   HUMAN TESTICULAR AROMATASE - IMMUNOCYTOCHEMICAL AND BIOCHEMICAL-STUDIES [J].
INKSTER, S ;
YUE, W ;
BRODIE, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (06) :1941-1947
[7]   EXPRESSION OF AROMATASE CYTOCHROME-P-450 IN PREMENOPAUSAL AND POSTMENOPAUSAL HUMAN OVARIES - AN IMMUNOCYTOCHEMICAL STUDY [J].
INKSTER, SE ;
BRODIE, AMH .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1991, 73 (04) :717-726
[8]   IMMUNOCYTOCHEMICAL STUDIES OF AROMATASE IN EARLY AND FULL-TERM HUMAN PLACENTAL TISSUES - COMPARISON WITH BIOCHEMICAL ASSAYS [J].
INKSTER, SE ;
BRODIE, AMH .
BIOLOGY OF REPRODUCTION, 1989, 41 (05) :889-898
[9]   AROMATIZATION OF TESTOSTERONE AND ESTROGEN-RECEPTOR LEVELS IN HUMAN-BREAST CANCER [J].
LI, K ;
ADAMS, JB .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1981, 14 (03) :269-272
[10]  
LIPTON A, 1987, CANCER, V59, P779, DOI 10.1002/1097-0142(19870215)59:4<779::AID-CNCR2820590419>3.0.CO