| Literature DB >> 6727363 |
W H McLaughlin, R A Milius, L M Gill, S J Adelstein, W D Bloomer.
Abstract
We have developed an oil- microcentrifuge assay system for analyzing the binding of [3H]estradiol in metabolically active MCF-7 and MDA human breast cancer cells. Complete separation of 2 X 10(6) cells from radioactive media can be achieved within 5 s of centrifugation at 12,000 rpm. The [3H]estradiol binding sites in MCF-7 cells are filled within 20 min of radioligand exposure. Using this assay, our MCF-7 cells contain approximately 15,000 high affinity and saturable binding sites. Binding is inhibited by estradiol and tamoxifen but not progesterone. There is no specific binding of [3H]estradiol in MDA cells. This assay is a rapid, sensitive and reproducible method for investigating hormone-receptor binding and ligand specificity in cultured cells; results compare favorably with those obtained by more complex and lengthy techniques.Entities:
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Year: 1984 PMID: 6727363 DOI: 10.1016/0022-4731(84)90355-8
Source DB: PubMed Journal: J Steroid Biochem ISSN: 0022-4731 Impact factor: 4.292