Stat3 Is a Negative Regulator of Intestinal Tumor Progression in ApcMin Mice

被引:136
作者
Musteanu, Monica [1 ]
Blaas, Leander [1 ]
Mair, Markus [1 ]
Schlederer, Michaela [1 ]
Bilban, Martin [2 ]
Tauber, Stefanie [2 ]
Esterbauer, Harald [2 ]
Mueller, Mathias [3 ]
Casanova, Emilio [1 ]
Kenner, Lukas [1 ,4 ]
Poli, Valeria [5 ]
Eferl, Robert [1 ]
机构
[1] Ludwig Boltzmann Inst Canc Res, A-1090 Vienna, Austria
[2] Med Univ Vienna, Dept Med & Chem Lab Diagnost, Vienna, Austria
[3] Univ Vet Med Vienna, Inst Genet & Anim Breeding, Vienna, Austria
[4] Med Univ Vienna, Clin Inst Pathol, Vienna, Austria
[5] Univ Turin, Dept Genet Biol & Biochem, Turin, Italy
基金
奥地利科学基金会;
关键词
APC; CEACAM1; Colorectal Cancer; COLITIS-ASSOCIATED CANCER; COLON-CANCER; SIGNAL TRANSDUCER; HYPERPLASTIC POLYPS; COLORECTAL-CANCER; GENE; TUMORIGENESIS; INFLAMMATION; ACTIVATION; PATHWAY;
D O I
10.1053/j.gastro.2009.11.049
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND AND AIMS: The transcription factor signal transducer and activator of transcription 3 (Stat3) has been considered to promote progression and metastasis of intestinal cancers. METHODS: We investigated the role of Stat3 in intestinal tumors using mice with conditional ablation of Stat3 in intestinal epithelial cells (Stat3(Delta IEC)). RESULTS: In the Apc(Min) mouse model of intestinal cancer, genetic ablation of Stat3 reduced the multiplicity of early adenomas. However, loss of Stat3 promoted tumor progression at later stages, leading to formation of invasive carcinomas, which significantly shortened the lifespan of Stat3(Delta IEC) Apc(Min/+) mice. Interestingly, loss of Stat3 in tumors of Apc(Min/+) mice had no significant impact on cell survival and angiogenesis, but promoted cell proliferation. A genome-wide expression analysis of Stat3-deficient tumors suggested that Stat3 might negatively regulate intestinal cancer progression via the cell adhesion molecule CEACAM1. CONCLUSIONS: Our data suggest that Stat3 impairs invasiveness of intestinal tumors. Therefore, therapeutic targeting of the Stat3 signaling pathway in intestinal cancer should be evaluated for adverse effects on tumor progression.
引用
收藏
页码:1003 / U257
页数:14
相关论文
共 44 条
[1]   Cell-specific pituitary gene expression profiles after treatment with leukemia inhibitory factor reveal novel modulators for proopiomelanocortin expression [J].
Abbud, RA ;
Kelleher, R ;
Melmed, S .
ENDOCRINOLOGY, 2004, 145 (02) :867-880
[2]   Essential role of STAT3 in the control of the acute-phase response as revealed by inducible gene activation in the liver [J].
Alonzi, T ;
Maritano, D ;
Gorgoni, B ;
Rizzuto, G ;
Libert, C ;
Poli, V .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (05) :1621-1632
[3]   TGF-β suppresses tumor progression in colon cancer by inhibition of IL-6 trans-signaling [J].
Becker, C ;
Fantini, MC ;
Schramm, C ;
Lehr, HA ;
Wirtz, S ;
Nikolaev, A ;
Burg, J ;
Strand, S ;
Kiesslich, R ;
Huber, S ;
Ito, H ;
Nishimoto, N ;
Yoshizaki, K ;
Nishimoto, N ;
Galle, PR ;
Blessing, M ;
Rose-John, S ;
Neurath, MF .
IMMUNITY, 2004, 21 (04) :491-501
[4]  
Boivin GP, 2004, COMPARATIVE MED, V54, P15
[5]   gp130-Mediated Stat3 Activation in Enterocytes Regulates Cell Survival and Cell-Cycle Progression during Colitis-Associated Tumorigenesis [J].
Bollrath, Julia ;
Phesse, Toby J. ;
von Burstin, Vivian A. ;
Putoczki, Tracy ;
Bennecke, Moritz ;
Bateman, Trudie ;
Nebelsiek, Tim ;
Lundgren-May, Therese ;
Canli, Oezge ;
Schwitalla, Sarah ;
Matthews, Vance ;
Schmid, Roland M. ;
Kirchner, Thomas ;
Arkan, Melek C. ;
Ernst, Matthias ;
Greten, Florian R. .
CANCER CELL, 2009, 15 (02) :91-102
[6]   PREVALENCE OF RAS GENE-MUTATIONS IN HUMAN COLORECTAL CANCERS [J].
BOS, JL ;
FEARON, ER ;
HAMILTON, SR ;
VERLAANDEVRIES, M ;
VANBOOM, JH ;
VANDEREB, AJ ;
VOGELSTEIN, B .
NATURE, 1987, 327 (6120) :293-297
[7]   Stat3 as an oncogene [J].
Bromberg, JF ;
Wrzeszczynska, MH ;
Devgan, G ;
Zhao, YX ;
Pestell, RG ;
Albanese, C ;
Darnell, JE .
CELL, 1999, 98 (03) :295-303
[8]   Overexpression of phosphorylated-STAT3 correlated with the invasion and metastasis of cutaneous squamous cell carcinoma [J].
Cai, SQ ;
Zheng, M ;
Chen, LR .
JOURNAL OF DERMATOLOGY, 2005, 32 (05) :354-360
[9]   Gene expression profile of adult T-cell acute lymphocytic leukemia identifies distinct subsets of patients with different response to therapy and survival [J].
Chiaretti, S ;
Li, XC ;
Gentleman, R ;
Vitale, A ;
Vignetti, M ;
Mandelli, F ;
Ritz, J ;
Foa, R .
BLOOD, 2004, 103 (07) :2771-2778
[10]   At the crossroads of inflammation and cancer [J].
Clevers, H .
CELL, 2004, 118 (06) :671-674