Expression of osteonectin mRNA in human breast tumours is inversely correlated with oestrogen receptor content

被引:30
作者
Graham, JD
Balleine, RL
Milliken, JS
Bilous, AM
Clarke, CL
机构
[1] UNIV SYDNEY,WESTMEAD HOSP,WESTMEAD INST CANC RES,WESTMEAD,NSW 2145,AUSTRALIA
[2] WESTMEAD HOSP,DEPT PATHOL ANAT,WESTMEAD,NSW 2145,AUSTRALIA
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
breast cancer; human biopsies; osteonectin; oestrogen receptor; RNA analysis; immunoblot analysis;
D O I
10.1016/S0959-8049(97)00182-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteonectin is a secreted glycoprotein which is detected in a number of normal and neoplastic human tissues in vivo. It is an extracellular matrix (ECM)-associated protein which is postulated to regulate cell migration, adhesion, proliferation and matrix mineralisation and previous reports suggest that it may be modulated by steroid hormones in target tissues. The aim of this study was to measure osteonectin mRNA and protein expression in breast tumour biopsies and compare these with oestrogen (ER) and progesterone receptor (PR) levels in the same tumours. An inverse correlation was seen between osteonectin mRNA expression and ER level. Samples with low ER protein expression had a mean osteonectin mRNA level which was almost 4-fold greater than the mean level of expression observed in tumours containing high concentrations of ER protein. This inverse correlation was statistically significant. Despite the strong inverse relationship between osteonectin mRNA levels and tumour ER content, no correlation was seen when osteonectin protein concentration was measured in tumour cytosols on immunoblots and compared to ER and PR levels in the same tumours. However, since it is a secreted protein, osteonectin protein expression may not reflect cellular osteonectin levels in breast tumours. In summary, these data suggest that ER-mediated suppression of osteonectin gene expression may contribute to the less aggressive characteristics associated with receptor-positive tumours and that loss of ER expression may lead to overexpression of osteonectin and contribute to a poorer differentiated, more invasive phenotype. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:1654 / 1660
页数:7
相关论文
共 33 条
[1]  
BELLAHCENE A, 1995, AM J PATHOL, V146, P95
[2]   PRODUCTION OF OSTEOCALCIN BY HUMAN-BONE CELLS-INVITRO - EFFECTS OF 1,25(OH)2D3, 24,25(OH)2D3, PARATHYROID-HORMONE, AND GLUCOCORTICOIDS [J].
BERESFORD, JN ;
GALLAGHER, JA ;
POSER, JW ;
RUSSELL, RGG .
METABOLIC BONE DISEASE & RELATED RESEARCH, 1984, 5 (05) :229-234
[3]   TRANSFORMING GROWTH-FACTOR-BETA MEDIATES THE PROGESTERONE SUPPRESSION OF AN EPITHELIAL METALLOPROTEINASE BY ADJACENT STROMA IN THE HUMAN ENDOMETRIUM [J].
BRUNER, KL ;
RODGERS, WH ;
GOLD, LI ;
KORC, M ;
HARGROVE, JT ;
MATRISIAN, LM ;
OSTEEN, KG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7362-7366
[4]  
CLARKE CL, 1990, J BIOL CHEM, V265, P12694
[5]  
GRAHAM JD, 1995, CANCER RES, V55, P5063
[6]   GLUCOCORTICOIDS INHIBIT THE ATTACHMENT OF OSTEOBLASTS TO BONE EXTRACELLULAR-MATRIX PROTEINS AND DECREASE BETA(1)-INTEGRIN LEVELS [J].
GRONOWICZ, GA ;
MCCARTHY, MB .
ENDOCRINOLOGY, 1995, 136 (02) :598-608
[7]   STROMELYSIN-3 EXPRESSION IN BREAST-CANCER BIOPSIES - CLINICOPATHOLOGICAL CORRELATIONS [J].
HAHNEL, E ;
HARVEY, JM ;
JOYCE, R ;
ROBBINS, PD ;
STERRETT, GF ;
HAHNEL, R .
INTERNATIONAL JOURNAL OF CANCER, 1993, 55 (05) :771-774
[8]   EXPRESSION OF STROMELYSIN-3 AND NM23 IN BREAST-CARCINOMA AND RELATED-TISSUES [J].
HAHNEL, E ;
DAWKINS, H ;
ROBBINS, P ;
HAHNEL, R .
INTERNATIONAL JOURNAL OF CANCER, 1994, 58 (02) :157-160
[9]  
HIROTA S, 1995, LAB INVEST, V72, P64
[10]  
KELM RJ, 1992, BLOOD, V80, P3112