MDR1 expression identifies human melanoma stem cells

被引:86
|
作者
Keshet, Gilmor I. [1 ]
Goldstein, Itarnar [1 ]
Itzhaki, Orit [2 ]
Cesarkas, Karen [1 ]
Shenhav, Liraz [1 ]
Yakirevitch, Arkadi [2 ]
Treves, Avraham J. [2 ]
Schachter, Jacob [2 ]
Amariglio, Ninette [1 ]
Rechavi, Gideon [1 ]
机构
[1] Tel Aviv Univ, Canc Res Ctr, Tel Hashomer & Sackler Sch Med, Sheba Med Ctr, IL-52621 Tel Aviv, Israel
[2] Tel Aviv Univ, Ella Inst Melanoma Res & Treatment, Tel Hashomer & Sackler Sch Med, Sheba Med Ctr, IL-52621 Tel Hashomer, Israel
关键词
multidrug resistance; melanoma; cancer stem cells; self-renewal; anchorage independence;
D O I
10.1016/j.bbrc.2008.02.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
ABC transporters are often found to be inherently expressed in a wide variety of stem cells, where they provide improved protection from toxins. We found a subpopulation of human melanoma cells expressing multidrug-resistance gene product 1 (MDR1). This fraction co-expresses the ABC transporters, ABCB5 and ABCC2 in addition to the stem cell markers, nanog and human telomerase reverse transcriptase (hTERT). The clonogenicity and self-renewal capacity of MDR1(+) melanoma cells were investigated in single cell settings using the limiting dilution assay. We found that the MDR1(+) cells, isolated by FACS sorting, demonstrated a higher self-renewal capacity than the MDR1(-) fraction, a key stem cell feature. Moreover, MDR1(+) cells had higher ability to form spheres in low attachment conditions, a hallmark of cancer. In conclusion, these novel findings imply that the MDR1(+) cells represent melanoma stem cells and thus should be considered as a unique cellular target for future anti-melanoma therapies. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:930 / 936
页数:7
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