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Chemical approaches to targeting drug resistance in cancer stem cells
被引:85
|作者:
Sotiropoulou, Panagiota A.
[1
]
Christodoulou, Michael S.
[2
]
Silvani, Alessandra
[2
]
Herold-Mende, Christel
[3
]
Passarella, Daniele
[2
]
机构:
[1] Univ Libre Bruxelles, Interdisciplinary Res Inst IRIBHM, B-1070 Brussels, Belgium
[2] Univ Milan, Dipartimento Chim, I-20133 Milan, Italy
[3] Heidelberg Univ, Dept Neurosurg, Div Expt Neurosurg, Heidelberg, Germany
关键词:
TUMOR-INITIATING CELLS;
ALDEHYDE DEHYDROGENASE ALDH;
GAMMA-SECRETASE INHIBITORS;
SMALL-MOLECULE INHIBITOR;
KAPPA-B PATHWAY;
GROWTH IN-VITRO;
OVARIAN-CANCER;
SELF-RENEWAL;
RADIATION-RESISTANCE;
MOUSE MODEL;
D O I:
10.1016/j.drudis.2014.05.002
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Cancer stem cells (CSCs) are a subpopulation of cancer cells with high clonogenic capacity and ability to reform parental tumors upon transplantation. Resistance to therapy has been shown for several types of CSC and, therefore, they have been proposed as the cause of tumor relapse. Consequently, much effort has been made to design molecules that can target CSCs specifically and sensitize them to therapy. In this review, we summarize the mechanisms underlying CSC resistance, the potential biological targets to overcome resistance and the chemical compounds showing activity against different types of CSC. The chemical compounds discussed here have been divided according to their origin: natural, natural-derived and synthetic compounds.
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页码:1547 / 1562
页数:16
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