Characterization of WWOX inactivation in murine mammary gland development

被引:30
作者
Abdeen, Suhaib K. [1 ]
Salah, Zaidoun [1 ,2 ,3 ]
Khawaled, Saleh [1 ]
Aqeilan, Rami I. [1 ,4 ]
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Sch, Lautenberg Ctr Immunol & Canc Res, IMRIC, IL-91120 Jerusalem, Israel
[2] Al Quds Univ, Al Quds Bard Honors Coll, East Jerusalem Abu Dies, Israel
[3] Al Quds Univ, Med Res Ctr, East Jerusalem Abu Dies, Israel
[4] Ohio State Univ, Ctr Comprehens Canc, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
基金
欧盟第七框架计划;
关键词
TUMOR-SUPPRESSOR; BREAST-CANCER; IN-VIVO; GENE; EXPRESSION; PROTEIN; MODEL; MICE; P53; FIBRONECTIN;
D O I
10.1002/jcp.24310
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The WW domain-containing oxidoreductase (WWOX) is commonly inactivated in multiple human cancers, including breast cancer. Wwox null mice die prematurely precluding adult tumor analysis. Nevertheless, aging Wwox-heterozygous mice at C3H genetic background develop higher incidence of mammary tumors. We recently generated a Wwox conditional knockout mouse in which loxp sites flank exon 1 in the Wwox allele and showed that total ablation of WWOX in these mice resembles that of conventional targeting of Wwox. Here, we report the characterization of WWOX ablation in mouse mammary gland using MMTV-Cre transgenic line. We demonstrated that WWOX ablation leads to impaired mammary ductal growth. Moreover, targeted deletion of WWOX is associated with increased levels of fibronectin, a component of the extracellular matrix. In addition, we showed that shRNA knockdown of WWOX in MCF10A breast epithelial cells dramatically increased fibronectin and is associated with enhanced cell survival and impaired growth in three-dimensional culture Matrigel assay. Taken together our results are consistent with a critical role for WWOX in normal breast development and tumorigenesis. J. Cell. Physiol. 228: 13911396, 2013. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:1391 / 1396
页数:6
相关论文
共 29 条
[1]
Wwox inactivation enhances mammary tumorigenesis [J].
Abdeen, S. K. ;
Salah, Z. ;
Maly, B. ;
Smith, Y. ;
Tufail, R. ;
Abu-Odeh, M. ;
Zanesi, N. ;
Croce, C. M. ;
Nawaz, Z. ;
Aqeilan, R. I. .
ONCOGENE, 2011, 30 (36) :3900-3906
[2]
Abdeen SK, 2012, J CELL PHYS IN PRESS
[3]
The WWOX tumor suppressor is essential for postnatal survival and normal bone metabolism [J].
Aqeilan, Rami I. ;
Hassan, Mohammad Q. ;
de Bruin, Alain ;
Hagan, John P. ;
Volinia, Stefano ;
Palumbo, Titziana ;
Hussain, Sadiq ;
Lee, Suk-Hee ;
Gaur, Tripti ;
Stein, Gary S. ;
Lian, Jane B. ;
Croce, Carlo M. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (31) :21629-21639
[4]
Targeted deletion of Wwox reveals a tumor suppressor function [J].
Aqeilan, Rami I. ;
Trapasso, Francesco ;
Hussain, Sadiq ;
Costinean, Stefan ;
Marshall, Dean ;
Pekarsky, Yuri ;
Hagan, John P. ;
Zanesi, Nicola ;
Kaou, Mohamed ;
Steint, Gary S. ;
Lian, Jane B. ;
Croce, Carlo M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (10) :3949-3954
[5]
WW domain-containing proteins, WWOX and YAP, compete for interaction with ErbB-4 and modulate its transcriptional function [J].
Aqeilan, RI ;
Donati, V ;
Palamarchuk, A ;
Trapasso, F ;
Kaou, M ;
Pekarsky, Y ;
Sudol, M ;
Croce, CM .
CANCER RESEARCH, 2005, 65 (15) :6764-6772
[6]
Physical and functional interactions between the Wwox tumor suppressor protein and the AP-2γ transcription factor [J].
Aqeilan, RI ;
Palamarchuk, A ;
Weigel, RJ ;
Herrero, JJ ;
Pekarsky, Y ;
Croce, CM .
CANCER RESEARCH, 2004, 64 (22) :8256-8261
[7]
Association of Wwox with ErbB4 in breast cancer [J].
Aqeilian, Rami I. ;
Donati, Valentina ;
Gaudio, Eugenio ;
Nicoloso, Milena S. ;
Sundvall, Maria ;
Korhonen, Anna ;
Lundin, Johan ;
Isola, Jorma ;
Sudol, Marius ;
Joensuu, Heikki ;
Croce, Carlo M. ;
Elenius, Klaus .
CANCER RESEARCH, 2007, 67 (19) :9330-9336
[8]
Bednarek AK, 2000, CANCER RES, V60, P2140
[9]
Bednarek AK, 2001, CANCER RES, V61, P8068
[10]
WW domain-containing oxidoreductase: a candidate tumor suppressor [J].
Chang, Nan-Shan ;
Hsu, Li-Jin ;
Lin, Yee-Shin ;
Lai, Feng-Jie ;
Sheu, Hamm-Ming .
TRENDS IN MOLECULAR MEDICINE, 2007, 13 (01) :12-22