An isoform of the coactivator AIB1 that increases hormone and growth factor sensitivity is overexpressed in breast cancer

被引:68
作者
Reiter, R
Wellstein, A
Riegel, AT [1 ]
机构
[1] Georgetown Univ, Med Ctr, Dept Oncol, Lombardi Canc Ctr, Washington, DC 20007 USA
[2] Georgetown Univ, Med Ctr, Dept Pharmacol, Lombardi Canc Ctr, Washington, DC 20007 USA
关键词
D O I
10.1074/jbc.M104744200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The AIB1 (amplified in breast cancer 1) protein is a coactivator that potentiates the transcriptional activity of nuclear hormone receptors, and its gene is amplified in a subset of human breast cancers. Here we report a splice variant of AIB1 mRNA that lacks the exon 3 sequence. We determined that the AIB-Delta3 mRNA encoded a 130-kDa protein that lacks the NH2-terminal basic helix-loop-helix and a portion of the PAS (Per-Arnt-Sim homology) dimerization domain. The 130-kDa protein was detected in MCF-7 breast cancer cells at levels that were 5-10% of the full-length protein, whereas in nontransformed mammary epithelium lines, the AIB-Delta3 protein was present at significantly lower levels compared with the full-length AIB1. Consistent with this finding, the abundance of AIB1-Delta3 mRNA was increased in human breast cancer specimens relative to that in normal breast tissue. To determine whether there were phenotypic changes associated with the overexpression of the AIB-Delta3 isoform, we performed functional reporter gene assays. These revealed that the ability of AIB1-Delta3 to promote transcription mediated by the estrogen or progesterone receptors was significantly greater than that of the full-length protein. Surprisingly, the AIB1-Delta3 isoform was also more effective than AIB1 in promoting transcription induced by epidermal growth factor. Overexpression of AIB1-Delta3 may thus play an important role in sensitizing breast tumor cells to hormone or growth factor stimulation.
引用
收藏
页码:39736 / 39741
页数:6
相关论文
共 47 条
[1]   Regulation of vascular endothelial growth factor (VEGF) expression is mediated by internal initiation of translation and alternative initiation of transcription [J].
Akiri, G ;
Nahari, D ;
Finkelstein, Y ;
Le, SY ;
Elroy-Stein, O ;
Levi, BZ .
ONCOGENE, 1998, 17 (02) :227-236
[2]   AIB1, a steroid receptor coactivator amplified in breast and ovarian cancer [J].
Anzick, SL ;
Kononen, J ;
Walker, RL ;
Azorsa, DO ;
Tanner, MM ;
Guan, XY ;
Sauter, G ;
Kallioniemi, OP ;
Trent, JM ;
Meltzer, PS .
SCIENCE, 1997, 277 (5328) :965-968
[3]   The CBP co-activator is a histone acetyltransferase [J].
Bannister, AJ ;
Kouzarides, T .
NATURE, 1996, 384 (6610) :641-643
[4]  
Bautista S, 1998, CLIN CANCER RES, V4, P2925
[5]   Functional interaction between the p160 coactivator proteins and the transcriptional enhancer factor family of transcription factors [J].
Belandia, B ;
Parker, MG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (40) :30801-30805
[6]   TRANSCRIPTION FACTOR TFIIB AND THE VITAMIN-D RECEPTOR COOPERATIVELY ACTIVATE LIGAND-DEPENDENT TRANSCRIPTION [J].
BLANCO, JCG ;
WANG, IM ;
TSAI, SY ;
TSAI, MJ ;
OMALLEY, BW ;
JURUTKA, PW ;
HAUSSLER, MR ;
OZATO, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (05) :1535-1539
[7]  
Bouras T, 2001, CANCER RES, V61, P903
[8]   NUCLEAR FACTOR RIP140 MODULATES TRANSCRIPTIONAL ACTIVATION BY THE ESTROGEN-RECEPTOR [J].
CAVAILLES, V ;
DAUVOIS, S ;
LHORSET, F ;
LOPEZ, G ;
HOARE, S ;
KUSHNER, PJ ;
PARKER, MG .
EMBO JOURNAL, 1995, 14 (15) :3741-3751
[9]   Nuclear receptor coactivator ACTR is a novel histone acetyltransferase and forms a multimeric activation complex with P/CAF and CBP/p300 [J].
Chen, HW ;
Lin, RJ ;
Schiltz, RL ;
Chakravarti, D ;
Nash, A ;
Nagy, L ;
Privalsky, ML ;
Nakatani, Y ;
Evans, RM .
CELL, 1997, 90 (03) :569-580
[10]   A secreted FGF-binding protein can serve as the angiogenic switch in human cancer [J].
Czubayko, F ;
LiaudetCoopman, EDE ;
Aigner, A ;
Tuveson, AT ;
Berchem, GJ ;
Wellstein, A .
NATURE MEDICINE, 1997, 3 (10) :1137-1140