Sur8 mediates tumorigenesis and metastasis in colorectal cancer
Author(s) -
Young Mi Lee,
Saluja Kaduwal,
Kug Hwa Lee,
JongChan Park,
Woo-Jeong Jeong,
KangYell Choi
Publication year - 2016
Publication title -
experimental and molecular medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.703
H-Index - 82
eISSN - 2092-6413
pISSN - 1226-3613
DOI - 10.1038/emm.2016.58
Subject(s) - gene knockdown , cancer research , metastasis , carcinogenesis , mapk/erk pathway , protein kinase b , pi3k/akt/mtor pathway , signal transduction , cell growth , colorectal cancer , biology , cancer , chemistry , cell culture , medicine , microbiology and biotechnology , genetics
Sur8, a scaffold protein of the Ras pathway, interacts with Ras and Raf and modulates the Ras-extracellular signal-regulated kinase (ERK) pathway. Here we show that Sur8 is overexpressed in established human colorectal cancer (CRC) cell lines and CRC patient tissues. Moreover, Sur8 expression is increased during liver metastasis in CRC patients. Sur8 knockdown decreases ERK and Akt activities in CRC cell lines, regardless of their K-Ras, B-Raf or PI3K mutation status. Overexpression or knockdown of Sur8 increases or decreases, respectively, the proliferation or transformation of CRC cell lines. Sur8 knockdown attenuates the migration and invasion of HCT116 CRC cells. Subcutaneous or orthotopic injection of HCT116 cells harboring a doxycycline (Dox)-mediated Sur8 knockdown system in nude mice resulted in decreased tumorigenic potential and inhibited the liver metastatic potential of HCT116 cells. Taken together, our data support the role of Sur8 as a promoter of tumorigenesis and liver metastasis in CRC through its modulation of the Ras-ERK and PI3K-Akt signaling pathways.
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