Loading…
Cisplatin enhances the cytotoxicity of fast neutrons in a murine lymphoma cell line1,2
The utilization of high linear energy transfer (LET) radiations, such as fast neutrons or carbon ions (hadrontherapy), offers promising perspectives in radiotherapy. While it is well known that by combining radiotherapy and chemotherapy, important therapeutic advantages can be obtained to cure cance...
Saved in:
Published in: | Canadian journal of physiology and pharmacology 2004-02, Vol.82 (2), p.140 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | |
container_issue | 2 |
container_start_page | 140 |
container_title | Canadian journal of physiology and pharmacology |
container_volume | 82 |
creator | Fischer, B Benzina, S Ganansia-Leymarie, V Denis, J M |
description | The utilization of high linear energy transfer (LET) radiations, such as fast neutrons or carbon ions (hadrontherapy), offers promising perspectives in radiotherapy. While it is well known that by combining radiotherapy and chemotherapy, important therapeutic advantages can be obtained to cure cancer, there have been, so far, very few investigations on the effects of treatments combining an irradiation with high-LET particles and cancer drugs. The present study was therefore undertaken to examine the effects of exposure to 65 MeV fast neutrons combined with cisplatin in a murine T cell lymphoma (RDM4) in vitro. The cells were irradiated at doses ranging from 2 to 8 Gy without or with addition of cisplatin shortly before the irradiation, at concentrations between 0.3 and 12.5 micro M. These treatments were applied concomitantly. Proliferation and apoptosis were assessed at different time intervals thereafter. The combination of irradiation with cisplatin was found to be more cytotoxic than either treatment alone. Furthermore, the cytotoxicity induced by this cotreatment resulted not only from apoptosis but also from other forms of cell death. |
format | article |
fullrecord | <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_journals_221677121</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>618219921</sourcerecordid><originalsourceid>FETCH-proquest_journals_2216771213</originalsourceid><addsrcrecordid>eNqNiksKwjAURYMoWD97eDi2kKTfeVFcgDgtIaQ0JU1q8gJ292bgAhwd7rlnQzLGaZU3Vcm2JKOUtnnJGd-TQwhTmnVbtBl5dTosRqC2oOworFQBcFQgV3ToPlpqXMENMIiAYFVE72yAVAuYo9dWgVnnZXSzAKmMAZMUu_IT2Q3CBHX-8Ugu99uze-SLd--oAvaTi96mq-ec1U3DOCv-ir6kLkHW</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>221677121</pqid></control><display><type>article</type><title>Cisplatin enhances the cytotoxicity of fast neutrons in a murine lymphoma cell line1,2</title><source>EBSCOhost SPORTDiscus with Full Text</source><creator>Fischer, B ; Benzina, S ; Ganansia-Leymarie, V ; Denis, J M</creator><creatorcontrib>Fischer, B ; Benzina, S ; Ganansia-Leymarie, V ; Denis, J M</creatorcontrib><description>The utilization of high linear energy transfer (LET) radiations, such as fast neutrons or carbon ions (hadrontherapy), offers promising perspectives in radiotherapy. While it is well known that by combining radiotherapy and chemotherapy, important therapeutic advantages can be obtained to cure cancer, there have been, so far, very few investigations on the effects of treatments combining an irradiation with high-LET particles and cancer drugs. The present study was therefore undertaken to examine the effects of exposure to 65 MeV fast neutrons combined with cisplatin in a murine T cell lymphoma (RDM4) in vitro. The cells were irradiated at doses ranging from 2 to 8 Gy without or with addition of cisplatin shortly before the irradiation, at concentrations between 0.3 and 12.5 micro M. These treatments were applied concomitantly. Proliferation and apoptosis were assessed at different time intervals thereafter. The combination of irradiation with cisplatin was found to be more cytotoxic than either treatment alone. Furthermore, the cytotoxicity induced by this cotreatment resulted not only from apoptosis but also from other forms of cell death.</description><identifier>ISSN: 0008-4212</identifier><identifier>EISSN: 1205-7541</identifier><identifier>CODEN: CJPPA3</identifier><language>eng</language><publisher>Ottawa: Canadian Science Publishing NRC Research Press</publisher><subject>Apoptosis ; Cancer ; Cells ; Chemotherapy ; Cytotoxicity ; Lymphoma ; Neutrons ; Radiation therapy</subject><ispartof>Canadian journal of physiology and pharmacology, 2004-02, Vol.82 (2), p.140</ispartof><rights>Copyright National Research Council of Canada Feb 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Fischer, B</creatorcontrib><creatorcontrib>Benzina, S</creatorcontrib><creatorcontrib>Ganansia-Leymarie, V</creatorcontrib><creatorcontrib>Denis, J M</creatorcontrib><title>Cisplatin enhances the cytotoxicity of fast neutrons in a murine lymphoma cell line1,2</title><title>Canadian journal of physiology and pharmacology</title><description>The utilization of high linear energy transfer (LET) radiations, such as fast neutrons or carbon ions (hadrontherapy), offers promising perspectives in radiotherapy. While it is well known that by combining radiotherapy and chemotherapy, important therapeutic advantages can be obtained to cure cancer, there have been, so far, very few investigations on the effects of treatments combining an irradiation with high-LET particles and cancer drugs. The present study was therefore undertaken to examine the effects of exposure to 65 MeV fast neutrons combined with cisplatin in a murine T cell lymphoma (RDM4) in vitro. The cells were irradiated at doses ranging from 2 to 8 Gy without or with addition of cisplatin shortly before the irradiation, at concentrations between 0.3 and 12.5 micro M. These treatments were applied concomitantly. Proliferation and apoptosis were assessed at different time intervals thereafter. The combination of irradiation with cisplatin was found to be more cytotoxic than either treatment alone. Furthermore, the cytotoxicity induced by this cotreatment resulted not only from apoptosis but also from other forms of cell death.</description><subject>Apoptosis</subject><subject>Cancer</subject><subject>Cells</subject><subject>Chemotherapy</subject><subject>Cytotoxicity</subject><subject>Lymphoma</subject><subject>Neutrons</subject><subject>Radiation therapy</subject><issn>0008-4212</issn><issn>1205-7541</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqNiksKwjAURYMoWD97eDi2kKTfeVFcgDgtIaQ0JU1q8gJ292bgAhwd7rlnQzLGaZU3Vcm2JKOUtnnJGd-TQwhTmnVbtBl5dTosRqC2oOworFQBcFQgV3ToPlpqXMENMIiAYFVE72yAVAuYo9dWgVnnZXSzAKmMAZMUu_IT2Q3CBHX-8Ugu99uze-SLd--oAvaTi96mq-ec1U3DOCv-ir6kLkHW</recordid><startdate>20040201</startdate><enddate>20040201</enddate><creator>Fischer, B</creator><creator>Benzina, S</creator><creator>Ganansia-Leymarie, V</creator><creator>Denis, J M</creator><general>Canadian Science Publishing NRC Research Press</general><scope>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FQ</scope><scope>8FV</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M3G</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>20040201</creationdate><title>Cisplatin enhances the cytotoxicity of fast neutrons in a murine lymphoma cell line1,2</title><author>Fischer, B ; Benzina, S ; Ganansia-Leymarie, V ; Denis, J M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_2216771213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Apoptosis</topic><topic>Cancer</topic><topic>Cells</topic><topic>Chemotherapy</topic><topic>Cytotoxicity</topic><topic>Lymphoma</topic><topic>Neutrons</topic><topic>Radiation therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fischer, B</creatorcontrib><creatorcontrib>Benzina, S</creatorcontrib><creatorcontrib>Ganansia-Leymarie, V</creatorcontrib><creatorcontrib>Denis, J M</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Canadian Business & Current Affairs Database</collection><collection>Canadian Business & Current Affairs Database (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>CBCA Reference & Current Events</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>Canadian journal of physiology and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fischer, B</au><au>Benzina, S</au><au>Ganansia-Leymarie, V</au><au>Denis, J M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cisplatin enhances the cytotoxicity of fast neutrons in a murine lymphoma cell line1,2</atitle><jtitle>Canadian journal of physiology and pharmacology</jtitle><date>2004-02-01</date><risdate>2004</risdate><volume>82</volume><issue>2</issue><spage>140</spage><pages>140-</pages><issn>0008-4212</issn><eissn>1205-7541</eissn><coden>CJPPA3</coden><abstract>The utilization of high linear energy transfer (LET) radiations, such as fast neutrons or carbon ions (hadrontherapy), offers promising perspectives in radiotherapy. While it is well known that by combining radiotherapy and chemotherapy, important therapeutic advantages can be obtained to cure cancer, there have been, so far, very few investigations on the effects of treatments combining an irradiation with high-LET particles and cancer drugs. The present study was therefore undertaken to examine the effects of exposure to 65 MeV fast neutrons combined with cisplatin in a murine T cell lymphoma (RDM4) in vitro. The cells were irradiated at doses ranging from 2 to 8 Gy without or with addition of cisplatin shortly before the irradiation, at concentrations between 0.3 and 12.5 micro M. These treatments were applied concomitantly. Proliferation and apoptosis were assessed at different time intervals thereafter. The combination of irradiation with cisplatin was found to be more cytotoxic than either treatment alone. Furthermore, the cytotoxicity induced by this cotreatment resulted not only from apoptosis but also from other forms of cell death.</abstract><cop>Ottawa</cop><pub>Canadian Science Publishing NRC Research Press</pub></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0008-4212 |
ispartof | Canadian journal of physiology and pharmacology, 2004-02, Vol.82 (2), p.140 |
issn | 0008-4212 1205-7541 |
language | eng |
recordid | cdi_proquest_journals_221677121 |
source | EBSCOhost SPORTDiscus with Full Text |
subjects | Apoptosis Cancer Cells Chemotherapy Cytotoxicity Lymphoma Neutrons Radiation therapy |
title | Cisplatin enhances the cytotoxicity of fast neutrons in a murine lymphoma cell line1,2 |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T09%3A15%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cisplatin%20enhances%20the%20cytotoxicity%20of%20fast%20neutrons%20in%20a%20murine%20lymphoma%20cell%20line1,2&rft.jtitle=Canadian%20journal%20of%20physiology%20and%20pharmacology&rft.au=Fischer,%20B&rft.date=2004-02-01&rft.volume=82&rft.issue=2&rft.spage=140&rft.pages=140-&rft.issn=0008-4212&rft.eissn=1205-7541&rft.coden=CJPPA3&rft_id=info:doi/&rft_dat=%3Cproquest%3E618219921%3C/proquest%3E%3Cgrp_id%3Ecdi_FETCH-proquest_journals_2216771213%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=221677121&rft_id=info:pmid/&rfr_iscdi=true |