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CD133-induced TM4SF5 expression promotes sphere growth via recruitment and blocking of protein tyrosine phosphatase receptor type F (PTPRF)

Cited 13 time in Web of Science Cited 14 time in Scopus
Authors

Kim, Somi; Cho, Chang Yun; Lee, Doohyung; Song, Dae-Geun; Kim, Hye-Jin; Jung, Jae Woo; Kim, Ji Eon; Park, Dasomi; Lee, Haesong; Um, Hyejin; Park, Jinsoo; Choi, Yoonjeong; Kim, Yoomin; Nam, Seo Hee; Lee, Jung Weon

Issue Date
2018-12
Publisher
Elsevier BV
Citation
Cancer Letters, Vol.438, pp.219-231
Abstract
CD133 is a surface marker of liver cancer stem cells. Transmembrane 4 L six family member 5 (TM4SF5) promotes sphere growth and circulation. However, it is unknown how CD133 and TM4SF5 cross-talk with each other for cancer stem cell properties. Here, we investigated the significance of inter-relationships between CD133, TM4SF5, CD44, and protein tyrosine phosphatase receptor type F (PTPRF) in a three-dimensional (3D) sphere growth system. We found that CD133 upregulated TM4SF5 and CD44, whereas TM4SF5 and CD44 did not affect CD133 expression. Signaling activity following CD133 phosphorylation caused TM4SF5 expression and sphere growth. TM4SF5 bound to CD133 and promoted c-Src activity for CD133 phosphorylation as a positive feedback loop, leading to CD133-mediated sphere growth that was inhibited by TM4SF5 inhibition or suppression. TM4SF5 also bound PTPRF and promoted paxillin phosphorylation. Decreased sphere growth upon CD133 suppression was recovered by TM4SF5 expression and partially by PTPRF suppression. TM4SF5 inhibition enhanced PTPRF levels and abolished PTPRF suppression-mediated sphere growth. Altogether, CD133-induced TM4SF5 expression and function were important for liver cancer sphere growth and may be a promising target to block metastasis.
ISSN
0304-3835
Language
English
URI
https://hdl.handle.net/10371/149736
DOI
https://doi.org/10.1016/j.canlet.2018.09.009
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