.
The cancer stem cell (CSC) model
depicts that tumors are hierarchically organized and maintained by CSCs lying
at the apex. CSCs have been "identified" in a variety of tumors
through the tumor-forming assay, in which tumor cells distinguished by a
certain cell surface marker (known as a CSC marker) were separately
transplanted into immunodeficient mice. In such assays, tumor cells positive
but not negative for the CSC marker (hereby defined as CSC(+) and CSC(-) cells,
respectively) have the ability of tumor-forming and generating both progenies.
However, here we show that CSC(+) and CSC(-) cells exhibit similar
proliferation in the native states. Using a cell tracing method, we demonstrate
that CSC(-) cells exhibit similar tumorigenesis and proliferation as CSC(+)
cells when they were co-transplanted into immunodeficient mice. Through serial
single-cell derived subline construction, we further demonstrated that CSC(+)
and CSC(-) cells from CSC marker expressing tumors could invariably generate
both progenies, and their characteristics are maintained among different
generations irrespective of the origins (CSC(+)-derived or CSC(-)-derived).
These findings demonstrate that tumorigenic cells cannot be distinguished by
common CSC markers alone and we propose that cautions should be taken when
using these markers independently to identify cancer stem cells due to the
phenotypic plasticity of tumor cells.
Source: Tumor cells positive and
negative for the common cancer stem cell markers are capable of initiating
tumor growth and generating both progenies. Huang SD (huangsd@smmu.edu.cn),
Yuan Y, Tang H, Liu XH, Fu CG, Cheng HZ, Bi JW, Yu YW, Gong DJ, Zhang W, Chen
J, Xu ZY. PLoS One. 2013;8(1):e54579
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