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Potential mechanisms of CD133 in cancer stem cells

Authors
Jang, Jae-WooSong, YeonhwaKim, Se-HyukKim, JoonSeo, Haeng Ran
Issue Date
1-9월-2017
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
CD133; Cancer stem cells (CSCs); Autophagy; Lipid metabolism; Reactive oxygen species (ROS); PI3K; Src; EGFR
Citation
LIFE SCIENCES, v.184, pp.25 - 29
Indexed
SCIE
SCOPUS
Journal Title
LIFE SCIENCES
Volume
184
Start Page
25
End Page
29
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/82284
DOI
10.1016/j.lfs.2017.07.008
ISSN
0024-3205
Abstract
Cancer stem cells (CSCs) have emerged as an underlying cause of cancer relapse and resistance to treatment. Initially, biomarkers were used to identify and isolate distinct cell populations. Several CSC markers have been identified from many types of tumors, and these markers are also being used for isolation and enrichment of CSCs. Cluster of differentiation CD133 is a well-characterized CSC marker, and it is involved in tumor cell proliferation, metastasis, tumorigenesis, and recurrence, as well as chemo- and radio-resistance. However, the mechanisms involved in CD133-mediated induction of CSC properties have not yet been elucidated. Here, we introduce and summarize the functions of CD133 in CSCs and suggest new mechanisms that may be of note in our approach to developing novel cancer therapies. (C) 2017 Elsevier Inc. All rights reserved.
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