Cancer Research Prevention Award  Advances in Breast Cancer Research
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[Cancer Research 54, 349-353, January 15, 1994]
© 1994 American Association for Cancer Research

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Estrogen Receptor Mutations in Tamoxifen-resistant Breast Cancer1

Pratima S. Karnik2, Sucheta Kulkarni, Xiao-Pu Liu, G. Thomas Budd and Ronald M. Bukowski

The Experimental Therapeutics Program, Cancer Center, Cleveland Clinic Research Foundation, Cleveland, Ohio 44195-5069

2 To whom requests for reprints should be addressed, at The Experimental Therapeutics Program, Cancer Center, Cleveland Clinic Research Foundation, 9500 Euclid Ave., Cleveland, OH 44195; hy5069.

Clinical resistance to antiestrogens like tamoxifen is a major problem in the treatment of hormone-dependent breast cancers. Since the estrogen receptor plays a central role in mediating the effects of estrogens and antiestrogens, we hypothesized that mutations in the estrogen receptor could be one mechanism by which breast tumors evolve from a hormone-dependent to a hormone-independent phenotype. The eight exons of the estrogen receptor complementary DNA from 20 tamoxifen-resistant and 20 tamoxifen-sensitive tumors were screened by Single Strand Conformation Polymorphism (SSCP), and the variant conformers were sequenced to identify the nucleotide changes. A 42-base pair replacement was found in exon 6 of a tamoxifen-resistant tumor. A single base pair deletion in exon 6 of a tamoxifen-resistant metastatic tumor but not in the primary tumor was detected in another case. If translated, both these mutations could generate truncated receptors with an intact DNA-binding domain and a defective hormone-binding domain that could constitutively activate transcription of previously estrogen-responsive genes. The remaining 18 of 20 tamoxifen-resistant tumors did not contain mutations in any of the 8 exons of the estrogen receptor complementary DNA. These results suggest that mutations in the estrogen receptor occur at a low frequency and do not account for most estrogen-independent, tamoxifen-resistant breast tumors.

1 Supported by a pilot program of the American Cancer Society.

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Received 10/21/93. Accepted 11/24/93.




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Copyright © 1994 by the American Association for Cancer Research.