Loading…
Effect of verapamil on daunorubicin accumulation in Ehrlich ascites tumor cells
Previous studies have demonstrated that verapamil may overcome resistance to anthracyclines. In vitro and in vivo experiments were performed on wild-type and resistant Ehrlich ascites tumor cells. Verapamil in concentrations of 25-50 microM enhances the accumulation of daunorubicin (DNR) in resistan...
Saved in:
Published in: | Cancer chemotherapy and pharmacology 1987-01, Vol.19 (1), p.35-39 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c311t-7c4ee81de0402541a02d37acae792e0ea2cf3203c83e450c98628e6e07eacc253 |
---|---|
cites | cdi_FETCH-LOGICAL-c311t-7c4ee81de0402541a02d37acae792e0ea2cf3203c83e450c98628e6e07eacc253 |
container_end_page | 39 |
container_issue | 1 |
container_start_page | 35 |
container_title | Cancer chemotherapy and pharmacology |
container_volume | 19 |
creator | FRICHE, E SKOVSGAARD, T NISSEN, N. I |
description | Previous studies have demonstrated that verapamil may overcome resistance to anthracyclines. In vitro and in vivo experiments were performed on wild-type and resistant Ehrlich ascites tumor cells. Verapamil in concentrations of 25-50 microM enhances the accumulation of daunorubicin (DNR) in resistant cells to the same level as in wild-type cells. No significant effect of verapamil on influx or nuclear binding could be demonstrated, indicating that verapamil enhances DNR uptake by blocking active drug extrusion. Exposure of cells to a high concentration of Ca2+ did not influence the effect of verapamil on DNR accumulation, suggesting a different mode of verapamil action apart from the Ca2+-blocking effect. Attempts to circumvent acquired resistance to DNR in vivo with verapamil showed that the combination of the two drugs was more toxic than DNR given alone. The LD10 of DNR was determined as 3 mg/kg and the LD10 of the combination, as 2.5 mg/kg. The therapeutic effect of verapamil at a dose of 50 mg/kg and DNR of 2.5 mg/kg increased the life span of the mice by 50%. No difference was seen in the wild-type tumor in vivo. These data lead us to conclude that verapamil can reverse DNR resistance completely, but that verapamil at non-toxic dosage only reduces DNR resistance by 50% in vivo. |
doi_str_mv | 10.1007/BF00296252 |
format | article |
fullrecord | <record><control><sourceid>pubmed_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1007_BF00296252</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3815723</sourcerecordid><originalsourceid>FETCH-LOGICAL-c311t-7c4ee81de0402541a02d37acae792e0ea2cf3203c83e450c98628e6e07eacc253</originalsourceid><addsrcrecordid>eNpFkE1Lw0AQhhdRaq1evAt78CREZz-S3Ry1tCoUetFz2E4mdCUfZTcR_PdGGuppGN6Hl5mHsVsBjwLAPL2sAWSeyVSesbnQSiZgtTpnc1BaJ6kBfcmuYvwCAC2UmrGZsiI1Us3ZdlVVhD3vKv5NwR1c42vetbx0Q9uFYefRt9whDs1Qu96Pybiv9qH2uOcuou8p8n5ousCR6jpes4vK1ZFuprlgn-vVx_It2Wxf35fPmwSVEH1iUBNZURJokKkWDmSpjENHJpcE5CRWSoJCq0ingLnNpKWMwNB4jEzVgj0cezF0MQaqikPwjQs_hYDiT0rxL2WE747wYdg1VJ7QycKY30_5-JGrq-Ba9PGEWQk2g1z9AvHQaN0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Effect of verapamil on daunorubicin accumulation in Ehrlich ascites tumor cells</title><source>SpringerLink Online Journals Archive Complete</source><creator>FRICHE, E ; SKOVSGAARD, T ; NISSEN, N. I</creator><creatorcontrib>FRICHE, E ; SKOVSGAARD, T ; NISSEN, N. I</creatorcontrib><description>Previous studies have demonstrated that verapamil may overcome resistance to anthracyclines. In vitro and in vivo experiments were performed on wild-type and resistant Ehrlich ascites tumor cells. Verapamil in concentrations of 25-50 microM enhances the accumulation of daunorubicin (DNR) in resistant cells to the same level as in wild-type cells. No significant effect of verapamil on influx or nuclear binding could be demonstrated, indicating that verapamil enhances DNR uptake by blocking active drug extrusion. Exposure of cells to a high concentration of Ca2+ did not influence the effect of verapamil on DNR accumulation, suggesting a different mode of verapamil action apart from the Ca2+-blocking effect. Attempts to circumvent acquired resistance to DNR in vivo with verapamil showed that the combination of the two drugs was more toxic than DNR given alone. The LD10 of DNR was determined as 3 mg/kg and the LD10 of the combination, as 2.5 mg/kg. The therapeutic effect of verapamil at a dose of 50 mg/kg and DNR of 2.5 mg/kg increased the life span of the mice by 50%. No difference was seen in the wild-type tumor in vivo. These data lead us to conclude that verapamil can reverse DNR resistance completely, but that verapamil at non-toxic dosage only reduces DNR resistance by 50% in vivo.</description><identifier>ISSN: 0344-5704</identifier><identifier>EISSN: 1432-0843</identifier><identifier>DOI: 10.1007/BF00296252</identifier><identifier>PMID: 3815723</identifier><identifier>CODEN: CCPHDZ</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Animals ; Antineoplastic agents ; Biological and medical sciences ; Biological Transport, Active - drug effects ; Calcium - pharmacology ; Carcinoma, Ehrlich Tumor - metabolism ; Carcinoma, Ehrlich Tumor - pathology ; Cell Line ; Daunorubicin - metabolism ; Daunorubicin - toxicity ; Dose-Response Relationship, Drug ; Drug Resistance ; Drug Synergism ; Female ; General aspects ; Glucose - pharmacology ; Medical sciences ; Mice ; Mice, Inbred Strains ; Pharmacology. Drug treatments ; Stimulation, Chemical ; Verapamil - pharmacology ; Verapamil - toxicity</subject><ispartof>Cancer chemotherapy and pharmacology, 1987-01, Vol.19 (1), p.35-39</ispartof><rights>1987 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c311t-7c4ee81de0402541a02d37acae792e0ea2cf3203c83e450c98628e6e07eacc253</citedby><cites>FETCH-LOGICAL-c311t-7c4ee81de0402541a02d37acae792e0ea2cf3203c83e450c98628e6e07eacc253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8208609$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3815723$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>FRICHE, E</creatorcontrib><creatorcontrib>SKOVSGAARD, T</creatorcontrib><creatorcontrib>NISSEN, N. I</creatorcontrib><title>Effect of verapamil on daunorubicin accumulation in Ehrlich ascites tumor cells</title><title>Cancer chemotherapy and pharmacology</title><addtitle>Cancer Chemother Pharmacol</addtitle><description>Previous studies have demonstrated that verapamil may overcome resistance to anthracyclines. In vitro and in vivo experiments were performed on wild-type and resistant Ehrlich ascites tumor cells. Verapamil in concentrations of 25-50 microM enhances the accumulation of daunorubicin (DNR) in resistant cells to the same level as in wild-type cells. No significant effect of verapamil on influx or nuclear binding could be demonstrated, indicating that verapamil enhances DNR uptake by blocking active drug extrusion. Exposure of cells to a high concentration of Ca2+ did not influence the effect of verapamil on DNR accumulation, suggesting a different mode of verapamil action apart from the Ca2+-blocking effect. Attempts to circumvent acquired resistance to DNR in vivo with verapamil showed that the combination of the two drugs was more toxic than DNR given alone. The LD10 of DNR was determined as 3 mg/kg and the LD10 of the combination, as 2.5 mg/kg. The therapeutic effect of verapamil at a dose of 50 mg/kg and DNR of 2.5 mg/kg increased the life span of the mice by 50%. No difference was seen in the wild-type tumor in vivo. These data lead us to conclude that verapamil can reverse DNR resistance completely, but that verapamil at non-toxic dosage only reduces DNR resistance by 50% in vivo.</description><subject>Animals</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Biological Transport, Active - drug effects</subject><subject>Calcium - pharmacology</subject><subject>Carcinoma, Ehrlich Tumor - metabolism</subject><subject>Carcinoma, Ehrlich Tumor - pathology</subject><subject>Cell Line</subject><subject>Daunorubicin - metabolism</subject><subject>Daunorubicin - toxicity</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Resistance</subject><subject>Drug Synergism</subject><subject>Female</subject><subject>General aspects</subject><subject>Glucose - pharmacology</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Pharmacology. Drug treatments</subject><subject>Stimulation, Chemical</subject><subject>Verapamil - pharmacology</subject><subject>Verapamil - toxicity</subject><issn>0344-5704</issn><issn>1432-0843</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><recordid>eNpFkE1Lw0AQhhdRaq1evAt78CREZz-S3Ry1tCoUetFz2E4mdCUfZTcR_PdGGuppGN6Hl5mHsVsBjwLAPL2sAWSeyVSesbnQSiZgtTpnc1BaJ6kBfcmuYvwCAC2UmrGZsiI1Us3ZdlVVhD3vKv5NwR1c42vetbx0Q9uFYefRt9whDs1Qu96Pybiv9qH2uOcuou8p8n5ousCR6jpes4vK1ZFuprlgn-vVx_It2Wxf35fPmwSVEH1iUBNZURJokKkWDmSpjENHJpcE5CRWSoJCq0ingLnNpKWMwNB4jEzVgj0cezF0MQaqikPwjQs_hYDiT0rxL2WE747wYdg1VJ7QycKY30_5-JGrq-Ba9PGEWQk2g1z9AvHQaN0</recordid><startdate>19870101</startdate><enddate>19870101</enddate><creator>FRICHE, E</creator><creator>SKOVSGAARD, T</creator><creator>NISSEN, N. I</creator><general>Springer</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19870101</creationdate><title>Effect of verapamil on daunorubicin accumulation in Ehrlich ascites tumor cells</title><author>FRICHE, E ; SKOVSGAARD, T ; NISSEN, N. I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-7c4ee81de0402541a02d37acae792e0ea2cf3203c83e450c98628e6e07eacc253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Animals</topic><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>Biological Transport, Active - drug effects</topic><topic>Calcium - pharmacology</topic><topic>Carcinoma, Ehrlich Tumor - metabolism</topic><topic>Carcinoma, Ehrlich Tumor - pathology</topic><topic>Cell Line</topic><topic>Daunorubicin - metabolism</topic><topic>Daunorubicin - toxicity</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Resistance</topic><topic>Drug Synergism</topic><topic>Female</topic><topic>General aspects</topic><topic>Glucose - pharmacology</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Pharmacology. Drug treatments</topic><topic>Stimulation, Chemical</topic><topic>Verapamil - pharmacology</topic><topic>Verapamil - toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FRICHE, E</creatorcontrib><creatorcontrib>SKOVSGAARD, T</creatorcontrib><creatorcontrib>NISSEN, N. I</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Cancer chemotherapy and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FRICHE, E</au><au>SKOVSGAARD, T</au><au>NISSEN, N. I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of verapamil on daunorubicin accumulation in Ehrlich ascites tumor cells</atitle><jtitle>Cancer chemotherapy and pharmacology</jtitle><addtitle>Cancer Chemother Pharmacol</addtitle><date>1987-01-01</date><risdate>1987</risdate><volume>19</volume><issue>1</issue><spage>35</spage><epage>39</epage><pages>35-39</pages><issn>0344-5704</issn><eissn>1432-0843</eissn><coden>CCPHDZ</coden><abstract>Previous studies have demonstrated that verapamil may overcome resistance to anthracyclines. In vitro and in vivo experiments were performed on wild-type and resistant Ehrlich ascites tumor cells. Verapamil in concentrations of 25-50 microM enhances the accumulation of daunorubicin (DNR) in resistant cells to the same level as in wild-type cells. No significant effect of verapamil on influx or nuclear binding could be demonstrated, indicating that verapamil enhances DNR uptake by blocking active drug extrusion. Exposure of cells to a high concentration of Ca2+ did not influence the effect of verapamil on DNR accumulation, suggesting a different mode of verapamil action apart from the Ca2+-blocking effect. Attempts to circumvent acquired resistance to DNR in vivo with verapamil showed that the combination of the two drugs was more toxic than DNR given alone. The LD10 of DNR was determined as 3 mg/kg and the LD10 of the combination, as 2.5 mg/kg. The therapeutic effect of verapamil at a dose of 50 mg/kg and DNR of 2.5 mg/kg increased the life span of the mice by 50%. No difference was seen in the wild-type tumor in vivo. These data lead us to conclude that verapamil can reverse DNR resistance completely, but that verapamil at non-toxic dosage only reduces DNR resistance by 50% in vivo.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>3815723</pmid><doi>10.1007/BF00296252</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0344-5704 |
ispartof | Cancer chemotherapy and pharmacology, 1987-01, Vol.19 (1), p.35-39 |
issn | 0344-5704 1432-0843 |
language | eng |
recordid | cdi_crossref_primary_10_1007_BF00296252 |
source | SpringerLink Online Journals Archive Complete |
subjects | Animals Antineoplastic agents Biological and medical sciences Biological Transport, Active - drug effects Calcium - pharmacology Carcinoma, Ehrlich Tumor - metabolism Carcinoma, Ehrlich Tumor - pathology Cell Line Daunorubicin - metabolism Daunorubicin - toxicity Dose-Response Relationship, Drug Drug Resistance Drug Synergism Female General aspects Glucose - pharmacology Medical sciences Mice Mice, Inbred Strains Pharmacology. Drug treatments Stimulation, Chemical Verapamil - pharmacology Verapamil - toxicity |
title | Effect of verapamil on daunorubicin accumulation in Ehrlich ascites tumor cells |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T21%3A26%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effect%20of%20verapamil%20on%20daunorubicin%20accumulation%20in%20Ehrlich%20ascites%20tumor%20cells&rft.jtitle=Cancer%20chemotherapy%20and%20pharmacology&rft.au=FRICHE,%20E&rft.date=1987-01-01&rft.volume=19&rft.issue=1&rft.spage=35&rft.epage=39&rft.pages=35-39&rft.issn=0344-5704&rft.eissn=1432-0843&rft.coden=CCPHDZ&rft_id=info:doi/10.1007/BF00296252&rft_dat=%3Cpubmed_cross%3E3815723%3C/pubmed_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c311t-7c4ee81de0402541a02d37acae792e0ea2cf3203c83e450c98628e6e07eacc253%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/3815723&rfr_iscdi=true |