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Identification of aneuploidy-selective antiproliferation compounds.
- Source :
-
Cell [Cell] 2011 Feb 18; Vol. 144 (4), pp. 499-512. - Publication Year :
- 2011
-
Abstract
- Aneuploidy, an incorrect chromosome number, is a hallmark of cancer. Compounds that cause lethality in aneuploid, but not euploid, cells could therefore provide new cancer therapies. We have identified the energy stress-inducing agent AICAR, the protein folding inhibitor 17-AAG, and the autophagy inhibitor chloroquine as exhibiting this property. AICAR induces p53-mediated apoptosis in primary mouse embryonic fibroblasts (MEFs) trisomic for chromosome 1, 13, 16, or 19. AICAR and 17-AAG, especially when combined, also show efficacy against aneuploid human cancer cell lines. Our results suggest that compounds that interfere with pathways that are essential for the survival of aneuploid cells could serve as a new treatment strategy against a broad spectrum of human tumors.<br /> (Copyright © 2011 Elsevier Inc. All rights reserved.)
- Subjects :
- Aminoimidazole Carboxamide analogs & derivatives
Aminoimidazole Carboxamide pharmacology
Animals
Antineoplastic Agents pharmacology
Apoptosis
Benzoquinones pharmacology
Cell Line
Cell Proliferation drug effects
Chloroquine pharmacology
Chromosome Segregation
Embryo, Mammalian cytology
Fibroblasts drug effects
Humans
Lactams, Macrocyclic pharmacology
Mice
Neoplasms drug therapy
Ribonucleotides pharmacology
Trisomy
Aneuploidy
Antineoplastic Agents isolation & purification
Drug Screening Assays, Antitumor
Neoplasms genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4172
- Volume :
- 144
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Cell
- Publication Type :
- Academic Journal
- Accession number :
- 21315436
- Full Text :
- https://doi.org/10.1016/j.cell.2011.01.017