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Originally published In Press as doi:10.1074/jbc.M108130200 on September 10, 2001

J. Biol. Chem., Vol. 276, Issue 46, 42863-42868, November 16, 2001
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Kruppel-like Factor 4 Regulates Laminin alpha 3A Expression in Mammary Epithelial Cells*

Kristi A. MillerDagger , Elizabeth A. EklundDagger §, Marie L. PeddinghausDagger , Zhengjin CaoDagger , Nisha FernandesDagger , Patrick W. TurkDagger , Bayar Thimmapaya, and Sigmund A. WeitzmanDagger §||

From the Departments of Dagger  Medicine, Division of Hematology/Oncology, and § Microbiology and Immunology, the Lurie Cancer Center, Northwestern University Medical School, and  Department of Medicine, Veterans Affairs Lakeside Medical Center, Chicago, Illinois 60611

Laminin-5, the major extracellular matrix protein produced by mammary epithelial cells, is composed of three chains (designated alpha 3A, beta 3, and gamma 2), each encoded by a separate gene. Laminin-5 is markedly down-regulated in breast cancer cells. Little is known about the regulation of laminin gene transcription in normal breast cells, nor about the mechanism underlying the down-regulation seen in cancer. In the present study, we cloned the promoter of the gene for the human laminin alpha 3A chain (LAMA3A) and investigated its regulation in functionally normal MCF10A breast epithelial cells and several breast cancer cell lines. Using site-directed mutagenesis of promoter-reporter constructs in transient transfection assays in MCF10A cells, we find that two binding sites for Kruppel-like factor 4 (KLF4/GKLF/EZF) are required for expression driven by the LAMA3A promoter. Electrophoretic mobility shift assays reveal absence of KLF4 binding activity in extracts from T47D, MDA-MB 231, ZR75-1, MDA-MB 436, and MCF7 breast cancer cells. Transient transfection of a plasmid expressing KLF4 activates transcription from the LAMA3A promoter in breast cancer cells. A reporter vector containing duplicate KLF4-binding sites in its promoter is expressed at high levels in MCF10A cells but at negligible levels in breast cancer cells. Thus, KLF4 is required for LAMA3A expression and absence of laminin alpha 3A in breast cancer cells appears, at least in part, attributable to the lack of KLF4 activity.


* This work was supported by United States ARMY Grants DAMD17-94-J-4466 and DAMD17-94-J-4291 and National Institutes of Health Grant 5T32CA09560 and CA74403.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EMBL Data Bank with accession number(s) AF279435.

|| To whom correspondence should be addressed: Olson 8276, 303 E. Chicago Ave., Chicago, IL 60611. Tel.: 312-908-5284; Fax: 312-908-5717; E-mail: s-weitzman@northwestern.edu.


Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.


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