IRF6 in development and disease - A mediator of quiescence and differentiation

被引:44
作者
Bailey, Caleb M. [1 ]
Hendrix, Mary J. C. [1 ,2 ]
机构
[1] Childrens Mem Res Ctr, Chicago, IL 60614 USA
[2] Northwestern Univ, Feinberg Sch Med, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
关键词
IRF6; maspin; cell differentiation; mammary gland; breast cancer;
D O I
10.4161/cc.7.13.6221
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Post utero development of the mammary gland is a complex developmental process characterized by states of rapid cell proliferation (branching morphogenesis) followed by functional differentiation (lactation) and the consequent apoptosis (involution) of the secretory mammary epithelial cell. This process is cyclical, such that involution returns the mammary gland to a near-virgin-like state capable of responding to morphogenic cues with each consecutive pregnancy. Importantly, many of the regulatory processes which oversee mammary gland development are corrupted or otherwise compromised during the development of breast cancer. For example, Interferon Regulatory Factor 6 (IRF6) is a novel protein with growth inhibitory properties that was initially identified in mammary epithelial cells through its interaction with maspin, a known tumor suppressor in normal breast tissue. Recent findings from our laboratory suggest that IRF6 functions synergistically with maspin to regulate mammary epithelial cell differentiation by acting on the cell cycle. This perspective focuses on the possible involvement of IRF6 in promoting differentiation by regulating exit from the cell cycle and entry into the G(0) phase of cellular quiescence, and how these new findings shed light on normal mammary gland development and the initiation and progression of breast cancer.
引用
收藏
页码:1925 / 1930
页数:6
相关论文
共 53 条
[1]
Interferon regulatory factor 6 promotes cell cycle arrest and is regulated by the proteasome in a cell cycle-dependent manner [J].
Bailey, Caleb M. ;
Abbott, Daniel E. ;
Margaryan, Naira V. ;
Khalkhali-Ellis, Zhila ;
Hendrix, Mary J. C. .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (07) :2235-2243
[2]
Biological functions of maspin [J].
Bailey, Caleb M. ;
Khalkhali-Ellis, Zhila ;
Seftor, Elisabeth A. ;
Hendrix, Mary J. C. .
JOURNAL OF CELLULAR PHYSIOLOGY, 2006, 209 (03) :617-624
[3]
Mammary serine protease inhibitor (maspin) binds directly to interferon regulatory factor 6 - Identification of a novel serpin partnership [J].
Bailey, CM ;
Khalkhali-Ellis, Z ;
Kondo, S ;
Margaryan, NV ;
Seftor, REB ;
Wheaton, WW ;
Amir, S ;
Pins, MR ;
Schutte, BC ;
Hendrix, MJC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (40) :34210-34217
[4]
Barnes BJ, 2003, CANCER RES, V63, P6424
[5]
CD14-dependent lipopolysaccharide-induced ß-defensin-2 expression in human tracheobronchial epithelium [J].
Becker, MN ;
Diamond, G ;
Verghese, MW ;
Randell, SH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (38) :29731-29736
[6]
The IKK inhibitor BMS-345541 affects multiple mitotic cell cycle transitions [J].
Blazkova, Hana ;
von Schubert, Conrad ;
Mikule, Keith ;
Schwab, Rebekka ;
Angliker, Nico ;
Schmuckli-Maurer, Jacqueline ;
Fernandez, Paula C. ;
Doxsey, Stephen ;
Dobbelaere, Dirk A. .
CELL CYCLE, 2007, 6 (20) :2531-2540
[7]
14-3-3σ is required to prevent mitotic catastrophe after DNA damage [J].
Chan, TA ;
Hermeking, H ;
Lengauer, C ;
Kinzler, KW ;
Vogelstein, B .
NATURE, 1999, 401 (6753) :616-620
[8]
Maspin alters the carcinoma proteome [J].
Chen, EI ;
Florens, L ;
Axelrod, FT ;
Monosov, E ;
Barbas, CF ;
Yates, JR ;
Felding-Habermann, B ;
Smith, JW .
FASEB JOURNAL, 2005, 19 (06) :1123-+
[9]
2 HUMAN HOMOLOGS OF SACCHAROMYCES-CEREVISIAE SW12/SNF2 AND DROSOPHILA-BRAHMA ARE TRANSCRIPTIONAL COACTIVATORS COOPERATING WITH THE ESTROGEN-RECEPTOR AND THE RETINOIC ACID RECEPTOR [J].
CHIBA, H ;
MURAMATSU, M ;
NOMOTO, A ;
KATO, H .
NUCLEIC ACIDS RESEARCH, 1994, 22 (10) :1815-1820
[10]
Role for Brm in cell growth control [J].
Coisy-Quivy, Marjorie ;
Disson, Olivier ;
Roure, Virginie ;
Muchardt, Christian ;
Blanchard, Jean-Marie ;
Dantonel, Jean-Christophe .
CANCER RESEARCH, 2006, 66 (10) :5069-5076