High-throughput screening for genes that prevent excess DNA replication in human cells and for molecules that inhibit them
Autor: | Rajarshi Guha, Wenge Zhu, Pinar Tuzmen, Jennifer Wichterman-Kouznetsova, Melvin L. DePamphilis, Scott E. Martin, Ronald L. Johnson, Chrissie Y. Lee, Marc Ferrer |
---|---|
Rok vydání: | 2012 |
Předmět: |
DNA Replication
DNA re-replication Cell division Cell growth DNA replication Antineoplastic Agents Suicide gene Biology Article General Biochemistry Genetics and Molecular Biology High-Throughput Screening Assays Cell biology Cell Line Tumor Data Interpretation Statistical Cancer cell Animals Humans Endoreduplication RNA Interference RNA Small Interfering Molecular Biology Gene Cell Proliferation |
Zdroj: | Methods. 57:234-248 |
ISSN: | 1046-2023 |
DOI: | 10.1016/j.ymeth.2012.03.031 |
Popis: | High-throughput screening (HTS) provides a rapid and comprehensive approach to identifying compounds that target specific biological processes as well as genes that are essential to those processes. Here we describe a HTS assay for small molecules that induce either DNA re-replication or endoreduplication (i.e. excess DNA replication) selectively in cells derived from human cancers. Such molecules will be useful not only to investigate cell division and differentiation, but they may provide a novel approach to cancer chemotherapy. Since induction of DNA re-replication results in apoptosis, compounds that selectively induce DNA re-replication in cancer cells without doing so in normal cells could kill cancers in vivo without preventing normal cell proliferation. Furthermore, the same HTS assay can be adapted to screen siR-NA molecules to identify genes whose products restrict genome duplication to once per cell division. Some of these genes might regulate the formation of terminally differentiated polyploid cells during normal human development, whereas others will prevent DNA re-replication during each cell division. Based on previous studies, we anticipate that one or more of the latter genes will prove to be essential for proliferation of cancer cells but not for normal cells, since many cancer cells are deficient in mechanisms that maintain genome stability. |
Databáze: | OpenAIRE |
Externí odkaz: |