Activation of p21(CIP1/WAF1) in mammary epithelium accelerates mammary tumorigenesis and promotes lung metastasis

被引:29
作者
Cheng, Xiaoyun [1 ,3 ]
Xia, Weiya [1 ]
Yang, Jer-Yen [1 ]
Hsu, Jennifer L. [1 ]
Chou, Chao-Kai [1 ]
Sun, Hui-Lung [1 ]
Wyszomierski, Shannon L. [1 ]
Mills, Gordon B. [1 ,2 ]
Muller, William J. [4 ]
Yu, Dihua [1 ,3 ]
Hung, Mien-Chie [1 ,3 ,5 ,6 ]
机构
[1] Univ Texas Houston, MD Anderson Canc Ctr, Dept Mol & Cellular Oncol, Houston, TX 77030 USA
[2] Univ Texas Houston, MD Anderson Canc Ctr, Dept Syst Biol, Houston, TX 77030 USA
[3] Univ Texas Houston, Grad Sch Biomed Sci, Houston, TX 77030 USA
[4] McGill Univ, Dept Med & Biochem, Montreal, PQ H3A 1A1, Canada
[5] China Med Univ & Hosp, Ctr Mol Med, Taichung 404, Taiwan
[6] China Med Univ & Hosp, Grad Inst Canc Biol, Taichung 404, Taiwan
关键词
p21; PKB/Akt; Mammary tumorigenesis; Lung metastasis; MEDIATED CELL-DEATH; COMPLEX-FORMATION; CENTER STAGE; IN-VIVO; AKT; PHOSPHORYLATION; KINASE; INDUCTION; SURVIVAL; CANCER;
D O I
10.1016/j.bbrc.2010.10.126
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
While p21 is well known to inhibit cyclin-CDK activity in the nucleus and it has also been demonstrated to have oncogenic properties in different types of human cancers. In vitro studies showed that the oncogenic function of p21 is closely related to its cytoplasmic localization. However, it is unclear whether cytoplasmic p21 contributes to tumorigenesis in vivo. To address this question, we generated transgenic mice expressing the Akt-phosphorylated form of p21 (p21T145D) in the mammary epithelium. The results showed that Akt-activated p21 was expressed in the cytoplasm of mammary epithelium. Overexpression of Akt-activated p21 accelerated tumor onset and promoted lung metastasis in MMTV/neu mice, providing evidence that p21, especially cytoplasmic phosphorylated p21, has an oncogenic role in promoting mammary tumorigenesis and metastasis. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:103 / 107
页数:5
相关论文
共 27 条
[1]   Apoptosis inhibitory activity of cytoplasmic p21Cip1/WAF1 in monocytic differentiation [J].
Asada, M ;
Yamada, T ;
Ichijo, H ;
Delia, D ;
Miyazono, K ;
Fukumuro, K ;
Mizutani, S .
EMBO JOURNAL, 1999, 18 (05) :1223-1234
[2]   Phosphorylation of HDM2 by Akt [J].
Ashcroft, M ;
Ludwig, RL ;
Woods, DB ;
Copeland, TD ;
Weber, HO ;
MacRae, EJ ;
Vousden, KH .
ONCOGENE, 2002, 21 (13) :1955-1962
[3]   Cell cycle and death control: long live Forkheads [J].
Burgering, BMT ;
Kops, GJPL .
TRENDS IN BIOCHEMICAL SCIENCES, 2002, 27 (07) :352-360
[4]   Akt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery [J].
Datta, SR ;
Dudek, H ;
Tao, X ;
Masters, S ;
Fu, HA ;
Gotoh, Y ;
Greenberg, ME .
CELL, 1997, 91 (02) :231-241
[5]   Tumorigenic activity of p21Waf1/Cip1 in thymic lymphoma [J].
De la Cueva, E. ;
Garcia-Cao, I. ;
Herranz, M. ;
Lopez, P. ;
Garcia-Palencia, P. ;
Flores, J. M. ;
Serrano, M. ;
Fernandez-Piqueras, J. ;
Martin-Caballero, J. .
ONCOGENE, 2006, 25 (29) :4128-4132
[6]   Adenovirus 5 E1A-mediated tumor suppression associated with E1A-mediated apoptosis in vivo [J].
Deng, J ;
Xia, WY ;
Hung, MC .
ONCOGENE, 1998, 17 (17) :2167-2175
[7]   P53-DEPENDENT INHIBITION OF CYCLIN-DEPENDENT KINASE-ACTIVITIES IN HUMAN FIBROBLASTS DURING RADIATION-INDUCED G1 ARREST [J].
DULIC, V ;
KAUFMANN, WK ;
WILSON, SJ ;
TLSTY, TD ;
LEES, E ;
HARPER, JW ;
ELLEDGE, SJ ;
REED, SI .
CELL, 1994, 76 (06) :1013-1023
[8]   Akt takes centre stage in cell-cycle deregulation [J].
El-Deiry, WS .
NATURE CELL BIOLOGY, 2001, 3 (03) :E71-E73
[9]   INHIBITION OF CDK2 ACTIVITY IN-VIVO BY AN ASSOCIATED 20K REGULATORY SUBUNIT [J].
GU, Y ;
TURCK, CW ;
MORGAN, DO .
NATURE, 1993, 366 (6456) :707-710
[10]   Induction of Akt Activity by Chemotherapy Confers Acquired Resistance [J].
Huang, Wei-Chien ;
Hung, Mien-Chie .
JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2009, 108 (03) :180-194