Microarray-based prediction of cytotoxicity of tumor cells to cantharidin
- Publication type:
- Journal article
- Metadata:
-
- Autoren
- Autoren-URL
- https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=fis-test-1&SrcAuth=WosAPI&KeyUT=WOS:000227097800013&DestLinkType=FullRecord&DestApp=WOS_CPL
- Externe Identifier
- Clarivate Analytics Document Solution ID: 898SZ
- PubMed Identifier: 15706417
- ISSN
- 1021-335X
- Ausgabe der Veröffentlichung
- 3
- Zeitschrift
- ONCOLOGY REPORTS
- Schlüsselwörter
- chemotherapy
- drug resistance
- hierarchical cluster analysis
- microarrays
- Paginierung
- 459 - 463
- Datum der Veröffentlichung
- 2005
- Status
- Published
- Titel
- Microarray-based prediction of cytotoxicity of tumor cells to cantharidin
- Sub types
- Article
- Ausgabe der Zeitschrift
- 13
Data source: Web of Science (Lite)
- Other metadata sources:
-
- Abstract
- Cantharidin (CAN) is the active principle of the Chinese blister beetle (Mylabris phalerata) which exerts profound cytotoxicity towards tumor cells. The aim of this study was to identify the molecular determinants of sensitivity and resistance of tumor cells to CAN. We mined the microarray database of the National Cancer Institute (NCI), for genes whose expression correlated with the IC(50) values for CAN of 60 cell lines of different tumor types. By COMPARE analysis Kendall's tau test, and false discovery rate (FDR) analysis, 21 out of 9706 genes or expressed sequence tags (ESTs) were identified. If the mRNA expression of the 21 genes or ESTs was subjected to hierarchical cluster analysis and cluster image mapping, sensitivity or resistance of the 60 cell lines to CAN was predictable with statistical significance. The majority of these genes are involved in DNA damage response, DNA repair, and/or apoptosis. In conclusion, sensitivity or resistance of tumor cells to CAN is multi-factorial in nature. DNA repair and apoptosis play a major role as determinants of cellular response to CAN. The present investigation represents a starting point to dissect the genes and molecular pathways responsible for cellular response to cantharidin in more detail.
- Addresses
- German Cancer Research Center, Im Neuenheimer Feld 280, D-69120 Heidelberg, Germany. thomas.efferth@web.de
- Autoren
- eISSN
- 1791-2431
- Externe Identifier
- PubMed Identifier: 15706417
- Open access
- false
- ISSN
- 1021-335X
- Ausgabe der Veröffentlichung
- 3
- Zeitschrift
- Oncology reports
- Schlüsselwörter
- Tumor Cells, Cultured
- Humans
- DNA Damage
- Cantharidin
- RNA, Messenger
- Enzyme Inhibitors
- Oligonucleotide Array Sequence Analysis
- Drug Screening Assays, Antitumor
- Cluster Analysis
- Predictive Value of Tests
- Gene Expression Profiling
- Apoptosis
- DNA Repair
- Drug Resistance, Neoplasm
- Databases, Genetic
- Sprache
- eng
- Medium
- Paginierung
- 459 - 463
- Datum der Veröffentlichung
- 2005
- Status
- Published
- Datum der Datenerfassung
- 2005
- Titel
- Microarray-based prediction of cytotoxicity of tumor cells to cantharidin.
- Sub types
- Journal Article
- Ausgabe der Zeitschrift
- 13
Data source: Europe PubMed Central
- Abstract
- Cantharidin (CAN) is the active principle of the Chinese blister beetle (Mylabris phalerata) which exerts profound cytotoxicity towards tumor cells. The aim of this study was to identify the molecular determinants of sensitivity and resistance of tumor cells to CAN. We mined the microarray database of the National Cancer Institute (NCI), for genes whose expression correlated with the IC(50) values for CAN of 60 cell lines of different tumor types. By COMPARE analysis Kendall's tau test, and false discovery rate (FDR) analysis, 21 out of 9706 genes or expressed sequence tags (ESTs) were identified. If the mRNA expression of the 21 genes or ESTs was subjected to hierarchical cluster analysis and cluster image mapping, sensitivity or resistance of the 60 cell lines to CAN was predictable with statistical significance. The majority of these genes are involved in DNA damage response, DNA repair, and/or apoptosis. In conclusion, sensitivity or resistance of tumor cells to CAN is multi-factorial in nature. DNA repair and apoptosis play a major role as determinants of cellular response to CAN. The present investigation represents a starting point to dissect the genes and molecular pathways responsible for cellular response to cantharidin in more detail.
- Autoren
- Autoren-URL
- https://www.ncbi.nlm.nih.gov/pubmed/15706417
- ISSN
- 1021-335X
- Ausgabe der Veröffentlichung
- 3
- Zeitschrift
- Oncol Rep
- Schlüsselwörter
- Apoptosis
- Cantharidin
- Cluster Analysis
- DNA Damage
- DNA Repair
- Databases, Genetic
- Drug Resistance, Neoplasm
- Drug Screening Assays, Antitumor
- Enzyme Inhibitors
- Gene Expression Profiling
- Humans
- Oligonucleotide Array Sequence Analysis
- Predictive Value of Tests
- RNA, Messenger
- Tumor Cells, Cultured
- Sprache
- eng
- Country
- Greece
- Paginierung
- 459 - 463
- Datum der Veröffentlichung
- 2005
- Status
- Published
- Datum, an dem der Datensatz öffentlich gemacht wurde
- 2005
- Titel
- Microarray-based prediction of cytotoxicity of tumor cells to cantharidin.
- Sub types
- Journal Article
- Ausgabe der Zeitschrift
- 13
Data source: PubMed
- Beziehungen:
- Property of