Activity of Drugs from Traditional Chinese Medicine toward Sensitive and MDR1- or MRP1-Overexpressing Multidrug-Resistant Human CCRF-CEM Leukemia Cells
- Publication type:
- Journal article
- Metadata:
-
- Autoren
- T Efferth
- M Davey
- A Olbrich
- G Rücker
- E Gebhart
- R Davey
- Autoren-URL
- https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=fis-test-1&SrcAuth=WosAPI&KeyUT=WOS:000176362900012&DestLinkType=FullRecord&DestApp=WOS_CPL
- DOI
- 10.1006/bcmd.2002.0492
- Externe Identifier
- Clarivate Analytics Document Solution ID: 565HC
- PubMed Identifier: 12064912
- ISSN
- 1079-9796
- Ausgabe der Veröffentlichung
- 2
- Zeitschrift
- BLOOD CELLS MOLECULES AND DISEASES
- Schlüsselwörter
- P-glycoprotein
- multidrug resistance-related protein 1
- traditional Chinese medicine
- chemotherapy
- Paginierung
- 160 - 168
- Datum der Veröffentlichung
- 2002
- Status
- Published
- Titel
- Activity of drugs from traditional Chinese medicine toward sensitive and MDR1- or MRP1-overexpressing multidrug-resistant human CCRF-CEM leukemia cells
- Sub types
- Article
- Ausgabe der Zeitschrift
- 28
Data source: Web of Science (Lite)
- Other metadata sources:
-
- Autoren
- Thomas Efferth
- Mary Davey
- Armin Olbrich
- Gerhard Rücker
- Erich Gebhart
- Ross Davey
- DOI
- 10.1006/bcmd.2002.0492
- ISSN
- 1079-9796
- Ausgabe der Veröffentlichung
- 2
- Zeitschrift
- Blood Cells, Molecules, and Diseases
- Sprache
- en
- Paginierung
- 160 - 168
- Datum der Veröffentlichung
- 2002
- Status
- Published
- Herausgeber
- Elsevier BV
- Herausgeber URL
- http://dx.doi.org/10.1006/bcmd.2002.0492
- Datum der Datenerfassung
- 2019
- Titel
- Activity of Drugs from Traditional Chinese Medicine toward Sensitive and MDR1- or MRP1-Overexpressing Multidrug-Resistant Human CCRF-CEM Leukemia Cells
- Ausgabe der Zeitschrift
- 28
Data source: Crossref
- Abstract
- There is considerable interest among basic and clinical researchers in novel drugs with activity against leukemia. The vast history of experience of traditional Chinese medicine (TCM) with medicinal plants may facilitate the identification of novel antileukemic compounds. In the present investigation, we tested 22 drugs for their activity toward CCRF-CEM cell lines: artesunate, artemisinin, baicalein, baicalin, berberine, bufalin, cantharidin, cephalotaxine, curcumin, daidzein, daidzin, diallyl disulfide, ginsenoside Rh2, glycyrrhizic acid, isonardosinon, homoharringtonine, nardosinon, nardofuran, puerarin, quercetin, tannic acid, and tetrahydronardosinon. As compounds from folk medicinal remedies are sometimes looked upon as alternative medicine with some hesitation or criticism, we investigated only chemically pure compounds and tested the drugs independently in two different laboratories in Germany and Australia. We used CCRF-CEM parental cells and doxorubicin-selected P-glycoprotein (P-gp)/MDR1-expressing CEM/ADR5000, vinblastine-selected P-gp/MDR1-expressing CEM/VLB(100), and epirubicin-selected multidrug resistance-related protein 1 (MRP1)-expressing CEM/E1000 sublines thereof. While CEM/ADR5000, CEM/VLB(100), and CEM/E1000 cells were highly resistant to the corresponding selecting agents, no or only minimal degrees of cross-resistance were observed to TCM drugs in both growth inhibition assay and MTT assay (range from 0.4- to 8-fold). Homoharringtonine, artesunate, and bufalin were most active among this panel of compounds. As shown by flow cytometry, artesunate significantly increased daunorubicin accumulation in CEM/E1000 cells, but not in CEM/VLB(100) or CCRF-CEM parental cells. Bufalin caused a small, but significant increase in daunorubicin accumulation in CEM/VLB(100) and CEM/E1000 cells. As artesunate and bufalin showed both antileukemic activity if applied alone and modulation activity in combination with daunorubicin in multidrug-resistant (MDR) cells, these two drugs may be suitable for novel combination treatment regimens to improve leukemia cell killing.
- Addresses
- Virtual Campus Rhineland-Palatinate, Mainz, Germany. efferth@vcrp.de
- Autoren
- Thomas Efferth
- Thomas Efferth
- Mary Davey
- Armin Olbrich
- Gerhard Rücker
- Erich Gebhart
- Ross Davey
- DOI
- 10.1006/bcmd.2002.0492
- eISSN
- 1096-0961
- Externe Identifier
- PubMed Identifier: 12064912
- Open access
- false
- ISSN
- 1079-9796
- Ausgabe der Veröffentlichung
- 2
- Zeitschrift
- Blood cells, molecules & diseases
- Schlüsselwörter
- Tumor Cells, Cultured
- Humans
- Daunorubicin
- Multidrug Resistance-Associated Proteins
- Drugs, Chinese Herbal
- Medicine, Chinese Traditional
- Drug Screening Assays, Antitumor
- Drug Resistance, Multiple
- Cell Division
- Dose-Response Relationship, Drug
- Drug Interactions
- Drug Resistance, Neoplasm
- ATP Binding Cassette Transporter, Subfamily B, Member 1
- Sprache
- eng
- Medium
- Paginierung
- 160 - 168
- Datum der Veröffentlichung
- 2002
- Status
- Published
- Datum der Datenerfassung
- 2002
- Titel
- Activity of drugs from traditional Chinese medicine toward sensitive and MDR1- or MRP1-overexpressing multidrug-resistant human CCRF-CEM leukemia cells.
- Sub types
- Comparative Study
- Journal Article
- Ausgabe der Zeitschrift
- 28
Data source: Europe PubMed Central
- Abstract
- There is considerable interest among basic and clinical researchers in novel drugs with activity against leukemia. The vast history of experience of traditional Chinese medicine (TCM) with medicinal plants may facilitate the identification of novel antileukemic compounds. In the present investigation, we tested 22 drugs for their activity toward CCRF-CEM cell lines: artesunate, artemisinin, baicalein, baicalin, berberine, bufalin, cantharidin, cephalotaxine, curcumin, daidzein, daidzin, diallyl disulfide, ginsenoside Rh2, glycyrrhizic acid, isonardosinon, homoharringtonine, nardosinon, nardofuran, puerarin, quercetin, tannic acid, and tetrahydronardosinon. As compounds from folk medicinal remedies are sometimes looked upon as alternative medicine with some hesitation or criticism, we investigated only chemically pure compounds and tested the drugs independently in two different laboratories in Germany and Australia. We used CCRF-CEM parental cells and doxorubicin-selected P-glycoprotein (P-gp)/MDR1-expressing CEM/ADR5000, vinblastine-selected P-gp/MDR1-expressing CEM/VLB(100), and epirubicin-selected multidrug resistance-related protein 1 (MRP1)-expressing CEM/E1000 sublines thereof. While CEM/ADR5000, CEM/VLB(100), and CEM/E1000 cells were highly resistant to the corresponding selecting agents, no or only minimal degrees of cross-resistance were observed to TCM drugs in both growth inhibition assay and MTT assay (range from 0.4- to 8-fold). Homoharringtonine, artesunate, and bufalin were most active among this panel of compounds. As shown by flow cytometry, artesunate significantly increased daunorubicin accumulation in CEM/E1000 cells, but not in CEM/VLB(100) or CCRF-CEM parental cells. Bufalin caused a small, but significant increase in daunorubicin accumulation in CEM/VLB(100) and CEM/E1000 cells. As artesunate and bufalin showed both antileukemic activity if applied alone and modulation activity in combination with daunorubicin in multidrug-resistant (MDR) cells, these two drugs may be suitable for novel combination treatment regimens to improve leukemia cell killing.
- Autoren
- Thomas Efferth
- Mary Davey
- Armin Olbrich
- Gerhard Rücker
- Erich Gebhart
- Ross Davey
- Autoren-URL
- https://www.ncbi.nlm.nih.gov/pubmed/12064912
- DOI
- 10.1006/bcmd.2002.0492
- ISSN
- 1079-9796
- Ausgabe der Veröffentlichung
- 2
- Zeitschrift
- Blood Cells Mol Dis
- Schlüsselwörter
- ATP Binding Cassette Transporter, Subfamily B, Member 1
- Cell Division
- Daunorubicin
- Dose-Response Relationship, Drug
- Drug Interactions
- Drug Resistance, Multiple
- Drug Resistance, Neoplasm
- Drug Screening Assays, Antitumor
- Drugs, Chinese Herbal
- Humans
- Medicine, Chinese Traditional
- Multidrug Resistance-Associated Proteins
- Tumor Cells, Cultured
- Sprache
- eng
- Country
- United States
- Paginierung
- 160 - 168
- PII
- S1079979602904924
- Datum der Veröffentlichung
- 2002
- Status
- Published
- Datum, an dem der Datensatz öffentlich gemacht wurde
- 2003
- Titel
- Activity of drugs from traditional Chinese medicine toward sensitive and MDR1- or MRP1-overexpressing multidrug-resistant human CCRF-CEM leukemia cells.
- Sub types
- Comparative Study
- Journal Article
- Ausgabe der Zeitschrift
- 28
Data source: PubMed
- Autoren
- T EFFERTH
- Zeitschrift
- Blood Cells Mol. Dis.
- Paginierung
- 160 - 168
- Datum der Veröffentlichung
- 2002
- Ausgabe der Zeitschrift
- 28
Data source: CiNii EN
- Autoren
- T EFFERTH
- Zeitschrift
- Blood Cells Mol. Dis.
- Paginierung
- 160 - 168
- Datum der Veröffentlichung
- 2002
- Ausgabe der Zeitschrift
- 28
Data source: CiNii JP
- Autoren
- T EFFERTH
- Zeitschrift
- Blood Cells Mol. Dis.
- Paginierung
- 160 - 168
- Datum der Veröffentlichung
- 2002
- Datum der Datenerfassung
- 2022
- Titel
- Activity of Drugs from Traditional Chinese Medicine toward Sensitive and MDR1- or MRP1-Overexpressing Multidrug-Resistant Human CCRF-CEM Leukemia Cells
- Ausgabe der Zeitschrift
- 28
Data source: Manual
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