Literature DB >> 31353791

The novel lncRNA CALIC upregulates AXL to promote colon cancer metastasis.

Yoshihiro Kawasaki1, Masaya Miyamoto1, Takeaki Oda1, Kosuke Matsumura1, Lumi Negishi1, Ryuichiro Nakato2, Sakiko Suda1, Naoko Yokota2, Katsuhiko Shirahige2, Tetsu Akiyama1.   

Abstract

Long non-coding RNAs (lncRNAs) are aberrantly expressed in many disease conditions, including cancer. Accumulating evidence indicates that some lncRNAs may play critical roles in cancer progression and metastasis. Here, we identify a set of lncRNAs that are upregulated in metastatic subpopulations isolated from colon cancer HCT116 cells in vivo and show that one of these lncRNAs, which we name CALIC, is required for the metastatic activity of colon cancer cells. We show that CALIC associates with the RNA-binding protein hnRNP-L and imparts specificity to hnRNP-L-mediated gene expression. Furthermore, we demonstrate that the CALIC/hnRNP-L complex upregulates the tyrosine kinase receptor AXL and that knockdown of CALIC or AXL using shRNA in colon cancer cells attenuates their ability to form metastases in mice. These results suggest that the CALIC/hnRNP-L complex enhances the metastatic potential of colon cancer cells.
© 2019 The Authors.

Entities:  

Keywords:  cancer metastasis; lncRNA; signal transduction

Mesh:

Substances:

Year:  2019        PMID: 31353791      PMCID: PMC6680119          DOI: 10.15252/embr.201847052

Source DB:  PubMed          Journal:  EMBO Rep        ISSN: 1469-221X            Impact factor:   8.807


  42 in total

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