TY - JOUR
T1 - Kruppel-like Factor 4 Regulates Laminin α3A Expression in Mammary Epithelial Cells
AU - Miller, Kristi A.
AU - Eklund, Elizabeth A.
AU - Peddinghaus, Marie L.
AU - Cao, Zhengjin
AU - Fernandes, Nisha
AU - Turk, Patrick W.
AU - Thimmapaya, Bayar
AU - Weitzman, Sigmund A.
N1 - Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2001/11/16
Y1 - 2001/11/16
N2 - Laminin-5, the major extracellular matrix protein produced by mammary epithelial cells, is composed of three chains (designated α3A, β3, and γ2), 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 α3A 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 α3A in breast cancer cells appears, at least in part, attributable to the lack of KLF4 activity.
AB - Laminin-5, the major extracellular matrix protein produced by mammary epithelial cells, is composed of three chains (designated α3A, β3, and γ2), 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 α3A 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 α3A in breast cancer cells appears, at least in part, attributable to the lack of KLF4 activity.
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U2 - 10.1074/jbc.M108130200
DO - 10.1074/jbc.M108130200
M3 - Article
C2 - 11551969
AN - SCOPUS:0035900766
SN - 0021-9258
VL - 276
SP - 42863
EP - 42868
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 46
ER -