Inverse Relationship Between Estrogen Receptor and Epidermal Growth Factor Receptor mRNA Levels in Human Breast Cancer Cell Lines

被引:25
作者
Lee, Christine S. L. [1 ]
Hall, Rosemary E. [1 ]
Alexander, Ian E. [1 ]
Koga, Masafumi [1 ]
Shine, John [1 ]
Sutherland, Robert L. [1 ]
机构
[1] St Vincents Hosp, Garvan Inst Med Res, Sydney, NSW 2010, Australia
基金
英国医学研究理事会;
关键词
estrogen receptor; epidermal growth factor receptor; breast cancer;
D O I
10.3109/08977199009108272
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Epidermal growth factor receptors (EGF-R) are present in a number of human breast cancer cell lines and tumor biopsies. Furthermore, it has been suggested that EGF-R levels are higher in estrogen receptor negative (ER-) than in ER+ human breast tumors and that EGF-R status may be a prognostic indicator in breast cancer. The present study was undertaken to establish whether there is a quantitative relationship between EGF-R and ER mRNA concentrations in a series of 10 well-characterized human breast cancer cell lines. All cell lines expressed detectable quantities of EGF-R mRNA by Northern analysis but the relative abundance of EGF-R mRNA varied more than 50-fold. Two transcripts corresponding to the 10.5- and 5.8-kb mRNAs described in other cell types were present but in different relative proportions in different cell lines. When these lines were divided into an ER + and an ER - group based on their ability to bind estradiol, ER - cell lines were shown to express significantly higher concentrations of EGF-R mRNA than did ER+ cell lines (p < 0.005). Furthermore, linear-regression analysis revealed a significant inverse relationship between ER and EGF-R mRNA concentrations both within the group of 10 human breast cancer cell lines as a whole (r=0.66) and within the 6 functionally ER+ lines (r=0.77). This demonstration of a significant (p < 0.005) inverse relationship between the concentrations of ER and EGF-R mRNAs in ER + cell lines raises the possibility of reciprocal regulation of the expression of these genes in human breast cancer.
引用
收藏
页码:97 / 103
页数:7
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