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

 

作者: LeeChristine S. L.,   HallRosemary E.,   AlexanderIan E.,   KogaMasafumi,   ShineJohn,   SutherlandRobert L.,  

 

期刊: Growth Factors  (Taylor Available online 1990)
卷期: Volume 3, issue 2  

页码: 97-103

 

ISSN:0897-7194

 

年代: 1990

 

DOI:10.3109/08977199009108272

 

出版商: Taylor&Francis

 

关键词: estrogen receptor;epidermal growth factor receptor;breast cancer

 

数据来源: Taylor

 

摘要:

AbstractEpidermal 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.

 

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