- Research article
- Open Access
- Open Peer Review
Clinicopathological significance of expression of p-c-Jun, TCF4 and beta-Catenin in colorectal tumors
© Takeda et al; licensee BioMed Central Ltd. 2008
- Received: 02 April 2008
- Accepted: 08 November 2008
- Published: 08 November 2008
A recent study has shown that phosphorylated c-Jun (p-c-Jun) interacts with TCF4 to form a complex that cooperatively enhances their transcriptional activity in the presence of β-Catenin, and that their interaction is critical for mouse intestinal tumorigenesis. To determine the significance of these three proteins in human colorectal tumors, we analyzed their nuclear expression by immunohistochemistry.
we analyzed their nuclear expression by immunohistochemistry using paraffin-embedded specimens of 68 resected colorectal tumors, which consisted of 19 adenomas, 14 high-grade intraepithelial neoplasia (HGINs) and 35 adenocarcinomas. We also analyzed the expression of MMP7, which has functional AP-1 and TCF binding sites in its promoter.
Expression of p-c-Jun, TCF4 and β-Catenin were significantly higher in adenomas than in the adjacent normal epithelia. Expression of p-c-Jun and β-Catenin in HGINs and adenocarcinomas were also significantly higher than in the adjacent normal epithelia. p-c-Jun expression, but not TCF4 and β-Catenin, was higher in adenomas and HGINs than in adenocarcinomas, in which p-c-Jun expression was negatively correlated with pT stage progression. Furthermore, significant correlations of expression were observed between p-c-Jun and TCF4 (r = 0.25, p = 0.04), TCF4 and β-Catenin (r = 0.30, p = 0.01), p-c-Jun and MMP7 (r = 0.26, p = 0.03), and TCF4 and MMP7 (r = 0.39, p = 0.0008), respectively.
These results suggest that nuclear expression of p-c-Jun, TCF4 and β-Catenin have important roles in human colorectal tumor development and that p-c-Jun may play a pivotal role in the earlier stages of tumor development.
- Nuclear Expression
- Percentage Score
- Match Pair Sign Rank Test
- Human Colorectal Tumor
Colorectal tumorigenesis is a multistep process involving genetic alterations of oncogenes and tumor suppressor genes, which lead to deregulation of a number of critical molecular pathways [1, 2]. One of the important genetic abnormalities is the mutation of the adenomatous polyposis coli (Apc) tumor suppressor gene, which results in deregulation of the APC/β-Catenin/T-cell factor 4 (TCF-4) signaling pathway [1–3]. β-Catenin is a 92 kDa protein that binds to the cytoplasmic tail of E-cadherin and plays an important role in the Wnt signal transduction [4, 5]. When mutations in the Apc gene or the β-Catenin gene itself occur, or when the Wnt pathway is up-regulated, β-Catenin accumulates in the cytoplasm and migrates to the nucleus . The aberrantly accumulated β-Catenin in the nucleus activates transcription by forming a complex with the TCF/LEF HMG box transcription factors family, including the TCF4, with the net result of the activation of the target genes that include c-myc, cyclin D1 and c-jun [2, 6, 7].
The proto-oncoprotein c-Jun is a major component of dimeric AP-1 transcription factor . Deregulated expression of c-Jun transforms rodent fibroblasts  depending on the induction of multiple c-Jun target genes [10–12], while the cell transformation by various oncogenes requires an increase of the c-Jun expression . An important mechanism in the stimulation of the AP-1 function is amino-terminal phosphorylation of c-Jun by the c-Jun N-terminal kinases (JNKs) [14, 15]. Phosphorylated c-Jun (p-c-Jun) is involved in stress-induced apoptosis, cellular proliferation and tumorigenesis . A recent study has shown that p-c-Jun interacts with TCF4 to form a complex that cooperatively enhances the transcriptional activity in the presence of β-Catenin and that the interaction dependent on the phosphorylation of c-Jun is critical for mouse intestinal tumorigenesis to occur . In addition, another recent study also shows physical and functional cooperation between AP-1 proteins including c-Jun and β-Catenin for the regulation of TCF-dependent genes . However, expressions of p-c-Jun in combination with TCF4 and β-Catenin have not been explored with regard to human colorectal tumors.
To determine the significance of p-c-Jun, TCF4 and β-Catenin in human colorectal tumors, we analyzed the nuclear expression of these proteins in resected colorectal tumors by immunohistochemistry. We also analyzed the expression of MMP7, which has functional AP-1 and TCF binding sites in its promoter .
Primary tumor specimens from 68 colorectal tumors were consecutively obtained by surgery or endoscopically from the Hokkaido University Medical Hospital between 2000 and 2003. Informed consent from patients were obtained for the use of resected tumor specimens. The patients with colorectal tumors consisted of 35 men and 33 women, with an average age at diagnosis of 63.8 years. The tumor classifications were determined according to the guidelines of the International Agency for Research on Cancer (IARC) and World Health Organization (WHO) . Tumor specimens were histopathologically diagnosed as adenomas (n = 19), high-grade intraepithelial neoplasia (HGINs) (n = 14) and adenocarcinomas (n = 35). The pTNM classifications were determined according to the guidelines of the International Union Against Cancer (UICC) . Adenocarcinoma represented 9 pT1, 2 pT2, 19 pT3 and 5 pT4 stage tumors, and 20 pN0, 7 pN1, 6 pN2 and 2 pN3 stage tumors.
The primary antibodies used for immunohistochemistry and immunofluorescence analyses included a rabbit polyclonal antibody to p-c-Jun (Phospho-c-Jun (Ser63) II; Cell Signaling, Cumming Center Beverly, MA) which recognizes c-Jun phosphorylated at Ser 63 [22, 23], a mouse anti-β-Catenin monoclonal antibody (IgG1, Clone 14; Transduction Laboratories, San Diego, CA) [24–28], a mouse anti-Tcf-4 monoclonal antibody (IgG2a, 6H5-3; Sigma, St. Louis, Missouri)  and a mouse anti-human MMP7 monoclonal antibody (IgG1, Clone 141-7B2; Daiichi Fine Chemical, Toyama, Japan) [30, 31].
Expression of p-c-Jun, TCF4, β-Catenin, and MMP7 was analyzed by immunohistochemistry. The avidin-biotin-peroxidase complex (ABC) method was used on 4-μm sections of formalin-fixed, paraffin-embedded tissues after deparaffinization. Briefly, deparaffinized tissue sections were microwaved in 0.01 M sodium citrate (pH 6.0) to retrieve the antigenicity for 25 min for p-c-Jun or 20 min for TCF4, β-Catenin and MMP7. The slides were allowed to cool for an additional 20 min in citrate buffer. The sections were then incubated with 3% (w/v) H2O2 in methanol to inhibit endogenous peroxidase activity, followed by incubation with normal goat serum (Vectastain Elite ABC kit; Vector Laboratories, Burlingame, CA) for p-c-Jun or with normal horse serum (Vectastain Elite ABC kit) for β-Catenin, TCF4 and MMP7 for 30 min at room temperature to block the nonspecific antibody binding sites. The sections were consecutively reacted with a rabbit polyclonal antibody against p-c-Jun (1:50 dilution) or with a mouse monoclonal antibody against TCF4 (1:200 dilution), β-Catenin (1:3200 dilution), or MMP7 (1:400 dilution) at 4°C overnight. After washing, biotinylated goat anti-rabbit IgG antibody (Vectastain Elite ABC kit) for p-c-Jun or biotinylated horse anti-mouse IgG antibody (Vectastain Elite ABC kit) for β-Catenin, TCF4 and MMP7 was applied for 30 min. After washing, avidin-biotin-peroxidase complex (Vectastain Elite ABC kit) was applied for 30 min followed by peroxidase detection with a mixture of 3,3'-diaminobenzidine (DAB; Vector Laboratories). To determine specificity of immunostaining, serial sections were similarly processed except that primary antibodies were omitted. Sections were counterstained with methyl green.
Two investigators (K.T. and I.K.) separately and independently evaluated the immunohistochemical staining without knowledge of the clinical data. The results were evaluated as immunohistochemistry (IHC) score, where the IHC score = (percentage of positive cells (percentage score)) × (staining intensity [which was scored as 0 to 3]) [26, 27, 32]. Significant differences in interpretation were resolved in conference. Such differences in interpretation only occurred in a small subset of specimens; discordance more than 30% in percentage score is 24% in total specimens of three types of tumors and their adjacent normal epithelia, and discordance more than one staining intensity score is 3%. Interobserver agreement on four staining intensity scores was also evaluated using the linearly weighted kappa statistics . The kappa value was 0.46 in all cases (data not shown) and interpreted as moderate agreement . In cases without significant discordance, scores of two observer were averaged.
Wilcoxon matched pairs signed ranks test was used to determine the differences between the tumors and the adjacent normal epithelia. The Mann-Whitney U test and Kruskal-Wallis test were used to determine the difference between two groups and among more than two groups, respectively. p < 0.05 was considered statistically significant. Spearman's rank correlation test was used to determine the correlation with staining intensity and percentage score.
For the immunofluorescent staining of p-c-Jun, TCF4 and β-Catenin, the sections were subjected to antigen retrieval by heating in 0.01 M sodium citrate (pH 6.0) in a microwave oven for 25 min. The slides were allowed to cool for an additional 20 min in citrate buffer. The sections were permeabilized in PBS containing 0.2% Triton X-100 (PBT) for 20 min at room temperature. Nonspecific binding sites were blocked with normal goat serum for 30 min at room temperature. The sections were incubated at 4°C overnight with a combination of the primary rabbit polyclonal antibody against p-c-Jun (1:2 dilution) and one of the mouse monoclonal antibodies against TCF4 (1:4 dilution) and β-Catenin (1:60 dilution). After washing, the sections were incubated for 90 min at room temperature with the mixture of Alexa Fluor 488-conjugated goat anti-rabbit IgG antibody and Alexa Fluor 568-conjugated goat anti-mouse IgG antibody which were highly cross-absorbed (Invitrogen, Eugene, OR). The sections were then evaluated and photographed under a fluorescence microscope. To determine specificity of the immunofluorescent staining, serial sections were similarly processed except that primary antibodies were omitted.
Nuclear expression of p-c-Jun, TCF4, and β-Catenin in colorectal adenomas, HGINs and adenocarcinomas compared with adjacent normal colon epithelia
In the tumor cells of adenomas, HGINs and adenocarcinomas, staining for p-c-Jun was mainly detected in the nucleus, while staining was observed in the nucleus and cytoplasm for TCF4, and in the nucleus, cytoplasm and cellular membrane for β-Catenin. Staining for MMP7 was observed in the cytoplasm of the tumor cells. Representative immunostaining patterns for these proteins are shown in Fig. 1. Intensity of the nuclear stainings for p-c-Jun, TCF4 and β-Catenin, and that of the cytoplasmic staining for MMP7 were scored as 0, 1, 2, or 3 (none, weak, moderate, or strong). Significant immunostaining was not detected in serial sections when the primary antibodies were omitted (data not shown).
p-c-Jun, TCF4 and β-Catenin in the adenomas, and p-c-Jun and β-Catenin in the HGINs and adenocarcinomas showed significantly higher scores than in their adjacent normal colorectal epithelia, respectively (p < 0.05 by Wilcoxon matched pairs signed ranks test) (Additional file 1-Supplemental Table S1). TCF4 in HGINs also tended to have higher scores than in the adjacent epithelia.
Nuclear expression of p-c-Jun, TCF4, and β-Catenin among adenomas, HGINs and adenocarcinomas
Relationship between nuclear expression of p-c-Jun, TCF4 and β-Catenin, and pT and pN stages in adenocarcinomas
Correlation between the nuclear expression of p-c-Jun, TCF4 and β-Catenin, and cytoplasmic MMP7 expression
Correlation among expression of p-c-Jun, TCF, β-Catenin and MMP7 in all colorectal tumors (n = 68).
Immunofluorescence analysis of p-c-Jun, TCF4 and β-Catenin
A recent study has shown that p-c-Jun interacts with TCF4 to form a complex that cooperatively enhances the transcriptional activity in the presence of β-Catenin, and that this interaction is critical for mouse intestinal tumorigenesis . However, only a few studies have examined c-Jun, TCF4 and β-Catenin expression in human colorectal tumors [17, 26–29]. In addition, there have been no studies that have analyzed their expression within the same specimens of human colorectal tumors. In the present study, we demonstrated that p-c-Jun, TCF4 and β-Catenin are frequently overexpressed in the nucleus of resected human colorectal tumors when compared to the adjacent normal epithelia by immunohistochemistry, suggesting that these three proteins may play important roles in human colorectal tumor development. The high expression of p-c-Jun in adenomas and HGINs, as compared with adenocarcinomas, and its negative correlation with pT stage progression in adenocarcinomas suggest that p-c-Jun may play a pivotal role in the earlier stages of tumor development. Furthermore, the multiple correlations among the expressions of these three proteins and MMP7, which is one of their downstream gene products, suggest that the interactions of p-c-Jun, TCF4 and β-Catenin that have been demonstrated in vitro  are also important in human colorectal tumor development.
Expression of c-Jun has been shown to be elevated in human colorectal adenomas and carcinomas when compared to adjacent normal epithelia . c-Jun's transcriptional activity is enhanced through the N-terminal phosphorylation of c-Jun at the serin residues 63 and 73 by JNKs . The present findings that the active phosphorylated form of c-Jun is also elevated in colorectal adenoma and carcinoma further support a potential role for c-Jun in human colorectal tumors.
While the published studies on c-Jun have not explored the correlations with pathological stages in adenocarcinoma , we have shown the higher p-c-Jun expression in adenomas and HGINs than in adenocarcinomas, and its negative correlation with pT stage progression in invasive cacinomas. The correlation of p-c-Jun expression with the earlier stages of human tumorigenesis is consistent with the recent in vivo studies for intestinal and liver tumors [17, 35, 36]. In the Apc Min mouse model of intestinal cancer, genetic abrogation of the c-Jun N-terminal phosphorylation or gut-specific conditional c-jun inactivation reduces tumor number and size, and prolongs the lifespan . In the mouse model of the chemically induced hepatocellular carcinomas, c-jun is required for the early stages of tumor development, and the number and size of hepatic tumors is dramatically reduced by c-jun inactivation after the tumors have been initiated [35, 36]. Furthermore, in human lung tumorigenesis, c-Jun is frequently overexpressed in an atypical area that includes dysplasia, and less frequently in lung cancer . Taken together, these results suggest that c-Jun, especially in its phosphorylated state, may play a pivotal role in the early stages of the tumor development, including that of human colorectal tumors.
The similarly high levels of expression of TCF4 in the nucleus of the colorectal normal epithelia and adenocarcinomas are consistent with the results of previous studies by immunohistochemistry and in situ hybridization [29, 38]. Interestingly, we found that the nuclear expression of TCF4 is significantly higher in adenomas than in the adjacent normal epithelia. Korinek et. al.  demonstrates that Apc -/- colon carcinoma cells contain a stable and constitutively active β-Catenin-TCF4 complex in the nuclei and that reintroduction of APC removes β-Catenin from TCF4 and abrogates the transcriptional activation of TCF4. These in vitro findings suggest that constitutive transcription of the TCF target genes, which is caused by the loss of APC function, may be a crucial event in the early transformation of the colonic epithelium. In this study, β-Catenin is also expressed in the nuclei in human colorectal adenomas and carcinomas including HGINs, as reported previously [26, 27, 39]. The elevated nuclear expression of both TCF4 and β-Catenin is in line with their theorized roles in early colorectal carcinogenesis.
Multiple correlations of expressions among p-c-Jun, TCF4 and β-Catenin, and their colocalization within nucleus shown by immunofluorescence analysis are consistent with two recent in vitro studies [17, 18]. One shows that p-c-Jun interacts with TCF4 to form a ternary complex containing c-Jun, TCF4 and β-Catenin and that p-c-Jun and TCF4 cooperatively activate the c-jun promoter in a β-Catenin-dependent manner . The other shows that the armadillo repeat domain of β-Catenin physically associates with the DNA-binding domain of c-Jun and that β-Catenin target genes, cyclin D1 and c-myc, are transcriptionally activated by c-Jun through TCF-binding site . Both studies show these interactions cooperatively enhance their transcriptional activities of promoters containing AP-1 and TCF-binding sites including c-jun promoter itself, which can promote a positive feedback loop for c-Jun expression, consistent with their correlations observed in human colorectal tumors. Significantly correlated expression of p-c-Jun and TCF4 with MMP7, which has functional AP-1 site and TCF4 site in its promoter , may support the hypothesis that interaction of p-c-Jun, TCF4 and β-Catenin enhance transcriptional activity and that the interaction is also important in human colorectal carcinogenesis.
These results suggest that nuclear expression of p-c-Jun, TCF4 and β-Catenin have important roles in human colorectal tumor development and that p-c-Jun may play a pivotal role in the earlier stages of this tumor development. Small molecule inhibitors of JNKs have been shown to inhibit c-Jun phosphorylation and the phosphorylation-dependent interactions between c-Jun and TCF4 . AP-1 blockade by a c-Jun dominant-negative mutant has been shown to inhibit growth of cancer cells includes colon cancer cells [40, 41]. Such inhibitors may have potential for use as preventive and therapeutic strategies against colorectal cancers.
- Kinzler K, Vogelstein B: Lessons from hereditary colorectal cancer. Cell. 1996, 87 (2): 159-170. 10.1016/S0092-8674(00)81333-1.View ArticlePubMedGoogle Scholar
- Chung D: The genetic basis of colorectal cancer: insights into critical pathways of tumorigenesis. Gastroenterology. 2000, 119 (3): 854-865. 10.1053/gast.2000.16507.View ArticlePubMedGoogle Scholar
- Wong N, Pignatelli M: Beta-catenin – a linchpin in colorectal carcinogenesis?. Am J Pathol. 2002, 160 (2): 389-401.View ArticlePubMedPubMed CentralGoogle Scholar
- Nelson W, Nusse R: Convergence of Wnt, beta-catenin, and cadherin pathways. Science. 2004, 303 (5663): 1483-1487. 10.1126/science.1094291.View ArticlePubMedPubMed CentralGoogle Scholar
- Takayama T, Shiozaki H, Shibamoto S, Oka H, Kimura Y, Tamura S, Inoue M, Monden T, Ito F, Monden M: Beta-catenin expression in human cancers. Am J Pathol. 1996, 148 (1): 39-46.PubMedPubMed CentralGoogle Scholar
- Barker N, Clevers H: Mining the Wnt pathway for cancer therapeutics. Nat Rev Drug Discov. 2006, 5 (12): 997-1014. 10.1038/nrd2154.View ArticlePubMedGoogle Scholar
- Tetsu O, McCormick F: Beta-catenin regulates expression of cyclin D1 in colon carcinoma cells. Nature. 1999, 398 (6726): 422-426. 10.1038/18884.View ArticlePubMedGoogle Scholar
- Eferl R, Wagner E: AP-1: A double-edged sword in tumorigenesis. NATURE REVIEWS CANCER. 2003, 3 (11): 859-868. 10.1038/nrc1209.View ArticlePubMedGoogle Scholar
- Schütte J, Minna J, Birrer M: Deregulated expression of human c-jun transforms primary rat embryo cells in cooperation with an activated c-Ha-ras gene and transforms rat-1a cells as a single gene. Proc Natl Acad Sci USA. 1989, 86 (7): 2257-2261. 10.1073/pnas.86.7.2257.View ArticlePubMedPubMed CentralGoogle Scholar
- Kinoshita I, Leaner V, Katabami M, Manzano R, Dent P, Sabichi A, Birrer M: Identification of cJun-responsive genes in Rat-1a cells using multiple techniques: increased expression of stathmin is necessary for cJun-mediated anchorage-independent growth. Oncogene. 2003, 22 (18): 2710-2722. 10.1038/sj.onc.1206371.View ArticlePubMedGoogle Scholar
- Leaner V, Kinoshita I, Birrer M: AP-1 complexes containing cJun and JunB cause cellular transformation of Rat1a fibroblasts and share transcriptional targets. Oncogene. 2003, 22 (36): 5619-5629. 10.1038/sj.onc.1206644.View ArticlePubMedGoogle Scholar
- Katabami M, Donninger H, Hommura F, Leaner V, Kinoshita I, Chick J, Birrer M: Cyclin A is a c-Jun target gene and is necessary for c-Jun-induced anchorage-independent growth in RAT1a cells. J Biol Chem. 2005, 280 (17): 16728-16738. 10.1074/jbc.M413892200.View ArticlePubMedGoogle Scholar
- Rapp U, Troppmair J, Beck T, Birrer M: Transformation by Raf and other oncogenes renders cells differentially sensitive to growth inhibition by a dominant negative c-jun mutant. Oncogene. 1994, 9 (12): 3493-3498.PubMedGoogle Scholar
- Dérijard B, Hibi M, Wu I, Barrett T, Su B, Deng T, Karin M, Davis R: JNK1: a protein kinase stimulated by UV light and Ha-Ras that binds and phosphorylates the c-Jun activation domain. Cell. 1994, 76 (6): 1025-1037. 10.1016/0092-8674(94)90380-8.View ArticlePubMedGoogle Scholar
- Kyriakis J, Banerjee P, Nikolakaki E, Dai T, Rubie E, Ahmad M, Avruch J, Woodgett J: The stress-activated protein kinase subfamily of c-Jun kinases. Nature. 1994, 369 (6476): 156-160. 10.1038/369156a0.View ArticlePubMedGoogle Scholar
- Behrens A, Sibilia M, Wagner E: Amino-terminal phosphorylation of c-Jun regulates stress-induced apoptosis and cellular proliferation. NATURE GENETICS. 1999, 21 (3): 326-329. 10.1038/6854.View ArticlePubMedGoogle Scholar
- Nateri A, Spencer-Dene B, Behrens A: Interaction of phosphorylated c-Jun with TCF4 regulates intestinal cancer development. Nature. 2005, 437 (7056): 281-285. 10.1038/nature03914.View ArticlePubMedGoogle Scholar
- Toualbi K, Güller M, Mauriz J, Labalette C, Buendia M, Mauviel A, Bernuau D: Physical and functional cooperation between AP-1 and beta-catenin for the regulation of TCF-dependent genes. Oncogene. 2007, 26 (24): 3492-3502. 10.1038/sj.onc.1210133.View ArticlePubMedGoogle Scholar
- Crawford H, Fingleton B, Gustavson M, Kurpios N, Wagenaar R, Hassell J, Matrisian L: The PEA3 subfamily of Ets transcription factors synergizes with beta-catenin-LEF-1 to activate matrilysin transcription in intestinal tumors. MOLECULAR AND CELLULAR BIOLOGY. 2001, 21 (4): 1370-1383. 10.1128/MCB.21.4.1370-1383.2001.View ArticleGoogle Scholar
- World Health Organization classification of Tumours: Colon and rectum. Pathology and Genetics of Tumours of the Digestive System. Lyon. Edited by: Stanley RH, Lauri AA. 2000, 2: 103-119.Google Scholar
- International union against cancer: Colon and rectum. TNM classification of malignant tumours. Edited by: Sobin LH, Wittekind CH. 2002, New Jersey: John Wiley & Sons, 72-76. 6Google Scholar
- Takagi Y, Ishikawa M, Nozaki K, Yoshimura S, Hashimoto N: Increased expression of phosphorylated c-Jun amino-terminal kinase and phosphorylated c-Jun in human cerebral aneurysms: role of the c-Jun amino-terminal kinase/c-Jun pathway in apoptosis of vascular walls. Neurosurgery. 2002, 51 (4): 997-1002. 10.1097/00006123-200210000-00027.PubMedGoogle Scholar
- Roth S, Shaikh A, Hennelly M, Li Q, Bindokas V, Graham C: Mitogen-activated protein kinases and retinal ischemia. Invest Ophthalmol Vis Sci. 2003, 44 (12): 5383-5395. 10.1167/iovs.03-0451.View ArticlePubMedGoogle Scholar
- Kildal W, Risberg B, Abeler V, Kristensen G, Sudbø J, Nesland J, Danielsen H: beta-catenin expression, DNA ploidy and clinicopathological features in ovarian cancer: a study in 253 patients. Eur J Cancer. 2005, 41 (8): 1127-1134. 10.1016/j.ejca.2005.01.022.View ArticlePubMedGoogle Scholar
- Horvath L, Henshall S, Lee C, Kench J, Golovsky D, Brenner P, O'Neill G, Kooner R, Stricker P, Grygiel J, et al: Lower levels of nuclear beta-catenin predict for a poorer prognosis in localized prostate cancer. Int J Cancer. 2005, 113 (3): 415-422. 10.1002/ijc.20599.View ArticlePubMedGoogle Scholar
- Wong S, Lo E, Lee K, Chan J, Hsiao W: Prognostic and diagnostic significance of beta-catenin nuclear immunostaining in colorectal cancer. Clin Cancer Res. 2004, 10 (4): 1401-1408. 10.1158/1078-0432.CCR-0157-03.View ArticlePubMedGoogle Scholar
- Wong S, Lo E, Chan A, Lee K, Hsiao W: Nuclear beta catenin as a potential prognostic and diagnostic marker in patients with colorectal cancer from Hong Kong. Mol Pathol. 2003, 56 (6): 347-352. 10.1136/mp.56.6.347.View ArticlePubMedPubMed CentralGoogle Scholar
- Ikenoue T, Ijichi H, Kato N, Kanai F, Masaki T, Rengifo W, Okamoto M, Matsumura M, Kawabe T, Shiratori Y, et al: Analysis of the beta-catenin/T cell factor signaling pathway in 36 gastrointestinal and liver cancer cells. Jpn J Cancer Res. 2002, 93 (11): 1213-1220.View ArticlePubMedGoogle Scholar
- Barker N, Huls G, Korinek V, Clevers H: Restricted high level expression of Tcf-4 protein in intestinal and mammary gland epithelium. AMERICAN JOURNAL OF PATHOLOGY. 1999, 154 (1): 29-35.View ArticlePubMedPubMed CentralGoogle Scholar
- Zeng Z, Shu W, Cohen A, Guillem J: Matrix metalloproteinase-7 expression in colorectal cancer liver metastases: evidence for involvement of MMP-7 activation in human cancer metastases. Clin Cancer Res. 2002, 8 (1): 144-148.PubMedGoogle Scholar
- Masaki T, Matsuoka H, Sugiyama M, Abe N, Goto A, Sakamoto A, Atomi Y: Matrilysin (MMP-7) as a significant determinant of malignant potential of early invasive colorectal carcinomas. Br J Cancer. 2001, 84 (10): 1317-1321. 10.1054/bjoc.2001.1790.View ArticlePubMedPubMed CentralGoogle Scholar
- Gee J, Barroso A, Ellis I, Robertson J, Nicholson R: Biological and clinical associations of c-jun activation in human breast cancer. Int J Cancer. 2000, 89 (2): 177-186. 10.1002/(SICI)1097-0215(20000320)89:2<177::AID-IJC13>3.0.CO;2-0.View ArticlePubMedGoogle Scholar
- Landis J, Koch G: The measurement of observer agreement for categorical data. Biometrics. 1977, 33 (1): 159-174. 10.2307/2529310.View ArticlePubMedGoogle Scholar
- Zhang W, Hart J, McLeod H, Wang H: Differential expression of the AP-1 transcription factor family members in human colorectal epithelial and neuroendocrine neoplasms. Am J Clin Pathol. 2005, 124 (1): 11-19. 10.1309/T1H2Y2CHWY7PD2BN.View ArticlePubMedGoogle Scholar
- Maeda S, Karin M: Oncogene at last – c-Jun promotes liver cancer in mice. Cancer Cell. 2003, 3 (2): 102-104. 10.1016/S1535-6108(03)00025-4.View ArticlePubMedGoogle Scholar
- Eferl R, Ricci R, Kenner L, Zenz R, David J, Rath M, Wagner E: Liver tumor development. c-Jun antagonizes the proapoptotic activity of p53. Cell. 2003, 112 (2): 181-192. 10.1016/S0092-8674(03)00042-4.View ArticlePubMedGoogle Scholar
- Szabo E, Riffe M, Steinberg S, Birrer M, Linnoila R: Altered cJUN expression: an early event in human lung carcinogenesis. Cancer Res. 1996, 56 (2): 305-315.PubMedGoogle Scholar
- Korinek V, Barker N, Morin P, van Wichen D, de Weger R, Kinzler K, Vogelstein B, Clevers H: Constitutive transcriptional activation by a beta-catenin-Tcf complex in APC-/- colon carcinoma. Science. 1997, 275 (5307): 1784-1787. 10.1126/science.275.5307.1784.View ArticlePubMedGoogle Scholar
- Chung G, Provost E, Kielhorn E, Charette L, Smith B, Rimm D: Tissue microarray analysis of beta-catenin in colorectal cancer shows nuclear phospho-beta-catenin is associated with a better prognosis. Clin Cancer Res. 2001, 7 (12): 4013-4020.PubMedGoogle Scholar
- Suto R, Tominaga K, Mizuguchi H, Sasaki E, Higuchi K, Kim S, Iwao H, Arakawa T: Dominant-negative mutant of c-Jun gene transfer: a novel therapeutic strategy for colorectal cancer. Gene Ther. 2004, 11 (2): 187-193. 10.1038/sj.gt.3302158.View ArticlePubMedGoogle Scholar
- Shimizu Y, Kinoshita I, Kikuchi J, Yamazaki K, Nishimura M, Birrer M, Dosaka-Akita H: Growth inhibition of non-small cell lung cancer cells by AP-1 blockade using a cJun dominant-negative mutant. Br J Cancer. 2008, 98 (5): 915-922. 10.1038/sj.bjc.6604267.View ArticlePubMedPubMed CentralGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/8/328/prepub
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