Trefoil factor family-3 is associated with aggressive behavior of colon cancer cells

被引:40
作者
Yio, XY
Zhang, JY
Babyatsky, M
Chen, AL
Lin, J
Fan, QX
Werther, JL
Itzkowitz, S
机构
[1] Mt Sinai Sch Med, Dr Henry D Janowitz Div Gastroenterol, Dept Med, New York, NY 10029 USA
[2] Mt Sinai Sch Med, Dept Pediat, New York, NY 10029 USA
关键词
apoptosis; colon cancer; invasion; metastasis; trefoil factor;
D O I
10.1007/s10585-005-6615-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and aim: Trefoil factor family 3 (TFF3) is expressed by intestinal epithelial cells and it mainly functions to protect the mucosa from injury. Expression of TFF3 has been correlated with a poor prognosis in patients with cancer, but little is known about whether TFF3 directly contributes to the malignant behavior of cancer cells. The present study was conducted to determine whether TFF3 expression contributes to the malignant behavior of cancer cells in vitro and in vivo. Methods: Two subclones of a metastatic rat colorectal cancer cell line, demonstrated previously to manifest aggressive (LN cells) and non-aggressive (LP cells) growth in vivo, were analyzed for expression of TFF3 and tested in assays of cancer cell migration, invasion, and apoptosis in vitro, and mortality in vivo. Results: The aggressive LN cell line endogenously expressed TFF3 and supported the transcription of a TFF3 promoter-driven reporter construct, whereas the non-aggressive LP cell line did not express TFF3. LN cells demonstrated enhanced migration, invasion, and less apoptosis compared to LP cells. Transfecting TFF3 into LP cells enhanced their ability to migrate, invade, block apoptosis, and behave more aggressively in vivo, thereby resembling the phenotype of LN cells. Conclusions: In rat colon cancer cells, both endogenous and constitutive expression of TFF3 correlates with an aggressive phenotype. These data provide direct evidence that TFF3 contributes to the malignant behavior of cancer cells.
引用
收藏
页码:157 / 165
页数:9
相关论文
共 40 条
[1]  
Argani P, 2001, CANCER RES, V61, P4320
[2]   The trefoil factor 1 participates in gastrointestinal cell differentiation by delaying G1-S phase transition and reducing apoptosis [J].
Bossenmeyer-Pourié, C ;
Kannan, R ;
Ribieras, S ;
Wendling, C ;
Stoll, I ;
Thim, L ;
Tomasetto, C ;
Rio, MC .
JOURNAL OF CELL BIOLOGY, 2002, 157 (05) :761-770
[3]   RHuKGF ameliorates symptoms in DSS and CD4+CD45RBHi T cell transfer mouse models of inflammatory bowel disease [J].
Byrne, FR ;
Farrell, CL ;
Aranda, R ;
Rex, KL ;
Scully, S ;
Brown, HL ;
Flores, SA ;
Gu, LH ;
Danilenko, DM ;
Lacey, DL ;
Ziegler, TR ;
Senaldi, G .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2002, 282 (04) :G690-G701
[4]  
Calnan DP, 1999, J PATHOL, V188, P312, DOI 10.1002/(SICI)1096-9896(199907)188:3<312::AID-PATH360>3.0.CO
[5]  
2-P
[6]   Loss of heterozygosity and promoter methylation, but not mutation, may underlie loss of TFF1 in gastric carcinoma [J].
Carvalho, R ;
Kayademir, T ;
Soares, P ;
Canedo, P ;
Sousa, S ;
Oliveira, C ;
Leistenschneider, P ;
Seruca, R ;
Gött, P ;
Blin, N ;
Carneiro, F ;
Machado, JC .
LABORATORY INVESTIGATION, 2002, 82 (10) :1319-1326
[7]   Anti-sense trefoil factor family-3 (intestinal trefoil factor) inhibits cell growth and induces chemosensitivity to adriamycin in human gastric cancer cells [J].
Chan, MWY ;
Chan, VYW ;
Leung, WK ;
Chan, KK ;
To, KF ;
Sung, JJY ;
Chan, FKL .
LIFE SCIENCES, 2005, 76 (22) :2581-2592
[8]   Expression of cytoplasmic TFF2 is a marker of tumor metastasis and negative prognostic factor in gastric cancer [J].
Dhar, DK ;
Wang, TC ;
Maruyama, L ;
Udagawa, J ;
Kubota, H ;
Fuji, T ;
Tachibana, M ;
Ono, T ;
Otani, H ;
Nagasue, N .
LABORATORY INVESTIGATION, 2003, 83 (09) :1343-1352
[9]   Intestinal trefoil factor controls the expression of the adenomatous polyposis coli-catenin and the E-cadherin-catenin complexes in human colon carcinoma cells [J].
Efstathiou, JA ;
Noda, M ;
Rowan, A ;
Dixon, C ;
Chinery, R ;
Jawhari, A ;
Hattori, T ;
Wright, NA ;
Bodmer, WF ;
Pignatelli, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (06) :3122-3127
[10]   Induction of scattering and cellular invasion by trefoil peptides in src- and RhoA-transformed kidney and colonic epithelial cells [J].
Emami, S ;
Le Floch, N ;
Bruyneel, E ;
Thim, L ;
May, F ;
Westley, B ;
Rio, MC ;
Mareel, M ;
Gespach, C .
FASEB JOURNAL, 2001, 15 (02) :351-361