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TLE4 promotes colorectal cancer progression through activation of JNK/c-Jun signaling pathway.


ABSTRACT: The Groucho transcriptional co-repressor TLE4 protein has been shown to be a tumor suppressor in a subset of acute myeloid leukemia. However, little is known about its role in development and progression of solid tumor. In this study, we found that the expression of TLE4 in colorectal cancer (CRC) tissues was significantly higher than that in their matched adjacent intestine epithelial tissues. In addition, high expression of TLE4 was significantly correlated with advanced Dukes stage, lymph node metastasis and poor prognosis of CRC. Moreover, enforced expression of TLE4 in CRC cell lines significantly enhanced proliferation, invasion and tumor growth. On the contrary, knock down of TLE4 repressed cell proliferation, invasion and tumor growth. Furthermore, our study exhibited that the TLE4 promoted cell proliferation and invasion partially via activation of JNK-c-Jun pathway and subsequently increased cyclinD1 and decreased P27Kip1 expression. In conclusion, these results suggested that TLE4, a potential prognostic biomarker for CRC, plays an important role in the development and progression of human CRC.

SUBMITTER: Wang SY 

PROVIDER: S-EPMC4823078 | biostudies-literature | 2016 Jan

REPOSITORIES: biostudies-literature

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TLE4 promotes colorectal cancer progression through activation of JNK/c-Jun signaling pathway.

Wang Shu-Yang SY   Gao Ke K   Deng Dan-Ling DL   Cai Juan-Juan JJ   Xiao Zhi-Yuan ZY   He Liu-Qing LQ   Jiao Hong-Li HL   Ye Ya-Ping YP   Yang Run-Wei RW   Li Ting-Ting TT   Liang Li L   Liao Wen-Ting WT   Ding Yan-Qing YQ  

Oncotarget 20160101 3


The Groucho transcriptional co-repressor TLE4 protein has been shown to be a tumor suppressor in a subset of acute myeloid leukemia. However, little is known about its role in development and progression of solid tumor. In this study, we found that the expression of TLE4 in colorectal cancer (CRC) tissues was significantly higher than that in their matched adjacent intestine epithelial tissues. In addition, high expression of TLE4 was significantly correlated with advanced Dukes stage, lymph nod  ...[more]

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