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Ras activation contributes to the maintenance and expansion of Sca-1(pos) cells in a mouse model of breast canceropen access

Authors
Kim, Ran-JuKim, Soo-RimRoh, Kyung-JinPark, Sang-BumPark, Jeong-RanKang, Kyung-SunKong, GuTang, BinwuYang, Yu-AnKohn, Ethan A.Wakefield, Lalage M.Nam, Jeong-Seok
Issue Date
Jan-2010
Publisher
ELSEVIER IRELAND LTD
Keywords
Cancer stem cell; Stem cell antigen-1; Ras
Citation
CANCER LETTERS, v.287, no.2, pp.172 - 181
Indexed
SCIE
SCOPUS
Journal Title
CANCER LETTERS
Volume
287
Number
2
Start Page
172
End Page
181
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/175610
DOI
10.1016/j.canlet.2009.06.010
ISSN
0304-3835
Abstract
The cancer stem cell (CSC) hypothesis proposes that CSCs are the root of cancer and cause cancer metastasis and recurrence. In this study, we examined whether Ras signaling is associated with sternness of the CSCs population characterized by the stem cell antigen (Sca-1) phenotype in a 4T1 syngeneic mouse model of breast cancer. The Sca-1(pos) putative CSCs had high levels of activated Ras and phosphorylated MEK (p-MEK), compared with counterparts. The Ras farnesylation inhibitor (FTI-277) suppressed the maintenance and expansion of CSCs. Therefore, selective inhibition of Ras activation may be useful for stem-specific cancer therapy.
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