Antitumor activity of an Ets protein, PEA3, in breast cancer cell lines MDA-MB-361DYT2 and BT474M1

被引:22
作者
Yu, Zhenming
Xia, Weiya
Wang, Hong-Ying
Wang, Shao-Chun
Pan, Yong
Kwong, Ka Yin
Hortobagyi, Gabriel N.
Hung, Mien-Chie
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Mol & Cellular Oncol, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
关键词
breast cancer; PEA3; antitumor activity;
D O I
10.1002/mc.20212
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Polyomavirus enhancer activator 3 (PEA3) is a member of the Ets family of transcription factors. We demonstrated in a previous study that, by downregulating the HER-2/neu oncogene at the transcriptional level, PEA3 can inhibit the growth and development into tumors of HER-2/neu-overexpressing ovarian cancer cells. Here, we establish stable clones of the human breast cancer cell line MDA-MB-361DYT2 that express PEA3 under the control of a tetracycline-inducible promoter. Ectopic expression of PEA3 in this cell line inhibited cell growth and resulted in cell cycle accumulation in the G1 phase. We demonstrate that expression of PEA3 in an orthotopic breast cancer model inhibited tumor growth and prolonged the survival of tumor-bearing mice. In a parallel experiment with another breast cancer cell line, BT474M1, we were unable to obtain stable PEA3-inducible transfectants, suggesting that PEA3 may exert a strong growth inhibition effect in this cell line. Indeed, PEA3 coupled with the liposome SN2 demonstrated therapeutic effects in mice bearing tumors induced by BT474M1. These results provide evidence for the antitumor activity of PEA3 in human breast cancers. (c) 2006 Wiley-Liss, Inc.
引用
收藏
页码:667 / 675
页数:9
相关论文
共 36 条
[1]
HER2/Neu and the Ets transcription activator PEA3 are coordinately upregulated in human breast cancer [J].
Benz, CC ;
OHagan, RC ;
Richter, B ;
Scott, GK ;
Chang, CH ;
Xiong, XH ;
Chew, K ;
Ljung, BM ;
Edgerton, S ;
Thor, A ;
Hassell, JA .
ONCOGENE, 1997, 15 (13) :1513-1525
[2]
ESX: A structurally unique Ets overexpressed early during human breast tumorigenesis [J].
Chang, CH ;
Scott, GK ;
Kuo, WL ;
Xiong, XH ;
Suzdaltseva, Y ;
Park, JW ;
Sayre, P ;
Erny, K ;
Collins, C ;
Gray, JW ;
Benz, CC .
ONCOGENE, 1997, 14 (13) :1617-1622
[3]
Differential expression patterns of the PEA3 group transcription factors through murine embryonic development [J].
ChotteauLelievre, A ;
Desbiens, X ;
Pelczar, H ;
Defossez, PA ;
deLaunoit, Y .
ONCOGENE, 1997, 15 (08) :937-952
[4]
Mechanisms controlling the transcription of matrix metalloproteinase genes in normal and neoplastic cells [J].
Crawford, HC ;
Matrisian, LM .
ENZYME & PROTEIN, 1996, 49 (1-3) :20-37
[5]
Cooperation of two PEA3/AP1 sites in uPA gene induction by TPA and FGF-2 [J].
D'Orazio, D ;
Besser, D ;
Marksitzer, R ;
Kunz, C ;
Hume, DA ;
Kiefer, B ;
Nagamine, Y .
GENE, 1997, 201 (1-2) :179-187
[6]
TIGHT CONTROL OF GENE-EXPRESSION IN MAMMALIAN-CELLS BY TETRACYCLINE-RESPONSIVE PROMOTERS [J].
GOSSEN, M ;
BUJARD, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (12) :5547-5551
[7]
THE COLLAGENASE GENE PROMOTER CONTAINS A TPA AND ONCOGENE-RESPONSIVE UNIT ENCOMPASSING THE PEA3 AND AP-1 BINDING-SITES [J].
GUTMAN, A ;
WASYLYK, B .
EMBO JOURNAL, 1990, 9 (07) :2241-2246
[8]
β3A-integrin downregulates the urokinase-type plasminogen activator receptor (u-PAR) through a PEA3/ets transcriptional silencing element in the u-PAR promoter [J].
Hapke, S ;
Gawaz, M ;
Dehne, K ;
Köhler, J ;
Marshall, JF ;
Graeff, H ;
Schmitt, M ;
Reuning, U ;
Lengyel, E .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (06) :2118-2132
[9]
PEA3 and AP-1 are required for constitutive IL-8 gene expression in hepatoma cells [J].
Iguchi, A ;
Kitajima, I ;
Yamakuchi, M ;
Ueno, S ;
Aikou, T ;
Kubo, T ;
Matsushima, K ;
Mukaida, N ;
Maruyama, I .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 279 (01) :166-171
[10]
THE ETS-DOMAIN - A NEW DNA-BINDING MOTIF THAT RECOGNIZES A PURINE-RICH CORE DNA-SEQUENCE [J].
KARIM, FD ;
URNESS, LD ;
THUMMEL, CS ;
KLEMSZ, MJ ;
MCKERCHER, SR ;
CELADA, A ;
VANBEVEREN, C ;
MAKI, RA ;
GUNTHER, CV ;
NYE, JA ;
GRAVES, BJ .
GENES & DEVELOPMENT, 1990, 4 (09) :1451-1453