Abstract | BACKGROUND: The Toll-like receptor 2 (TLR2)-driven tissue response may promote neoangiogenesis and tumour growth by mechanisms that are poorly understood. METHODS: We investigated the expression levels of TLR2 and associated- miRNAs in colorectal carcinoma (CRC) tissues and cell lines using real-time PCR, northern blotting and western blotting. Survival curver was generated by Log-Rank test and the role of TLR2 signalling in tumour invasion and migration was determined by transwell analysis kits. RESULTS: We observed that the tissues from CRC patients express relatively high levels of TLR2. Targeting TLR2 markedly reduces the invasion and migration of CRC cells. We also found that miR-143, a putative tumour suppressor that is down-regulated in CRC tissues, reduces the invasion and migration of CRC cells primarily via TLR2. Utilising a xenograft mouse model, we demonstrated that re-expression of miR-143 inhibits CRC cell colonisation in vivo. CONCLUSION: miR-143 blocks the TLR2 signalling pathway in human CRC cells. This knowledge may pave the way for new clinical applications utilising miR-143 mimics in the treatment of patients with CRC.
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Authors | Haiyan Guo, Ying Chen, Xiaobo Hu, Guanxiang Qian, Shengfang Ge, Jianjun Zhang |
Journal | Molecular cancer
(Mol Cancer)
Vol. 12
Pg. 77
(Jul 17 2013)
ISSN: 1476-4598 [Electronic] England |
PMID | 23866094
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- MIRN143 microRNA, human
- MicroRNAs
- Toll-Like Receptor 2
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Topics |
- Animals
- Base Pairing
- Base Sequence
- Cell Line, Tumor
- Cell Movement
(genetics)
- Colorectal Neoplasms
(genetics, metabolism, pathology)
- Disease Models, Animal
- Gene Expression
- Humans
- Mice
- MicroRNAs
(chemistry, genetics)
- Neoplasm Invasiveness
- Neoplasm Metastasis
- Toll-Like Receptor 2
(genetics, metabolism)
- Transplantation, Heterologous
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