Loading…
Comparative study of the radiosensitizing and cell cycle effects of vinflunine and vinorelbine, in vitro
Vinca alkaloids are an important class of anticancer agents and semisynthetic vinca alkaloids are developed to improve the therapeutic index of this class of drugs. In the present study, a direct comparison was made between vinflunine and vinorelbine regarding their radiosensitizing and cell cycle e...
Saved in:
Published in: | BMC cancer 2008-02, Vol.8, p.65 |
---|---|
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 | |
container_start_page | 65 |
container_title | BMC cancer |
container_volume | 8 |
creator | Simoens, Cindy Lardon, Filip Pauwels, Bea De Pooter, Christel M J Lambrechts, Hilde A J Pattyn, Greet G O Breillout, Fabienne Vermorken, Jan B |
description | Vinca alkaloids are an important class of anticancer agents and semisynthetic vinca alkaloids are developed to improve the therapeutic index of this class of drugs. In the present study, a direct comparison was made between vinflunine and vinorelbine regarding their radiosensitizing and cell cycle effects.
Four human tumour cell lines were tested under identical experimental conditions, using equitoxic concentrations of vinflunine and vinorelbine.
Vinflunine and vinorelbine induced a comparable radiosensitizing effect (p-value never below 0.01) when cells were incubated for 24 h immediately prior to radiation. Regarding the cell cycle effects, a statistically significant concentration-dependent G2/M block was seen after 24 h incubation with vinorelbine in all tested cell lines. Similar results, with small cell line-related differences, were observed with vinflunine.
The radiosensitizing effects of both semisynthetic vinca alkaloids were comparable (not statistically different) and nearly always cell line-specific and concentration-dependent. The cell cycle effects could be related to the observed radiosensitizing effects. Considering the more favourable toxicity profile of vinflunine, this agent might be more promising than vinorelbine for chemoradiation studies in the clinic. |
doi_str_mv | 10.1186/1471-2407-8-65 |
format | article |
fullrecord | <record><control><sourceid>pubmed</sourceid><recordid>TN_cdi_pubmed_primary_18312675</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>18312675</sourcerecordid><originalsourceid>FETCH-LOGICAL-p545-33b6117fa7dd6e4bed2ec8644b65db6e67ec2fd84cc11ac6c08daa76a6e521713</originalsourceid><addsrcrecordid>eNo9j0tLxDAUhYMgzji6dSn5AVZz27y2UnzBgJvZD2ly40TatDTpQP311ufq8B0-DhxCroDdAmh5B1xBUXKmCl1IcULW_8WKnKf0zhgozfQZWYGuoJRKrMmh7rvBjCaHI9KUJzfT3tN8QDoaF_qEMYUcPkJ8oyY6arFtqZ1tixS9R5vTl34M0bdTDBG_pQX7Edtm4Rsa4sJ57C_IqTdtwsvf3JDd48Oufi62r08v9f22GAQXRVU1EkB5o5yTyBt0JVotOW-kcI1EqdCW3mluLYCx0jLtjFHSSBQlKKg25PpndpiaDt1-GENnxnn_97j6BJafWFk</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Comparative study of the radiosensitizing and cell cycle effects of vinflunine and vinorelbine, in vitro</title><source>PubMed Central</source><creator>Simoens, Cindy ; Lardon, Filip ; Pauwels, Bea ; De Pooter, Christel M J ; Lambrechts, Hilde A J ; Pattyn, Greet G O ; Breillout, Fabienne ; Vermorken, Jan B</creator><creatorcontrib>Simoens, Cindy ; Lardon, Filip ; Pauwels, Bea ; De Pooter, Christel M J ; Lambrechts, Hilde A J ; Pattyn, Greet G O ; Breillout, Fabienne ; Vermorken, Jan B</creatorcontrib><description>Vinca alkaloids are an important class of anticancer agents and semisynthetic vinca alkaloids are developed to improve the therapeutic index of this class of drugs. In the present study, a direct comparison was made between vinflunine and vinorelbine regarding their radiosensitizing and cell cycle effects.
Four human tumour cell lines were tested under identical experimental conditions, using equitoxic concentrations of vinflunine and vinorelbine.
Vinflunine and vinorelbine induced a comparable radiosensitizing effect (p-value never below 0.01) when cells were incubated for 24 h immediately prior to radiation. Regarding the cell cycle effects, a statistically significant concentration-dependent G2/M block was seen after 24 h incubation with vinorelbine in all tested cell lines. Similar results, with small cell line-related differences, were observed with vinflunine.
The radiosensitizing effects of both semisynthetic vinca alkaloids were comparable (not statistically different) and nearly always cell line-specific and concentration-dependent. The cell cycle effects could be related to the observed radiosensitizing effects. Considering the more favourable toxicity profile of vinflunine, this agent might be more promising than vinorelbine for chemoradiation studies in the clinic.</description><identifier>EISSN: 1471-2407</identifier><identifier>DOI: 10.1186/1471-2407-8-65</identifier><identifier>PMID: 18312675</identifier><language>eng</language><publisher>England</publisher><subject>Antineoplastic Agents, Phytogenic - chemistry ; Antineoplastic Agents, Phytogenic - pharmacology ; Breast Neoplasms - pathology ; Carcinoma - pathology ; Carcinoma, Non-Small-Cell Lung - pathology ; Cell Cycle - drug effects ; Cell Line, Tumor - drug effects ; Cell Line, Tumor - radiation effects ; Dose-Response Relationship, Drug ; Female ; Gamma Rays ; Humans ; Lung Neoplasms - pathology ; Microtubules - drug effects ; Molecular Structure ; Radiation-Sensitizing Agents - pharmacology ; Structure-Activity Relationship ; Tongue Neoplasms - pathology ; Urinary Bladder Neoplasms - pathology ; Vinblastine - analogs & derivatives ; Vinblastine - chemistry ; Vinblastine - pharmacology</subject><ispartof>BMC cancer, 2008-02, Vol.8, p.65</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18312675$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Simoens, Cindy</creatorcontrib><creatorcontrib>Lardon, Filip</creatorcontrib><creatorcontrib>Pauwels, Bea</creatorcontrib><creatorcontrib>De Pooter, Christel M J</creatorcontrib><creatorcontrib>Lambrechts, Hilde A J</creatorcontrib><creatorcontrib>Pattyn, Greet G O</creatorcontrib><creatorcontrib>Breillout, Fabienne</creatorcontrib><creatorcontrib>Vermorken, Jan B</creatorcontrib><title>Comparative study of the radiosensitizing and cell cycle effects of vinflunine and vinorelbine, in vitro</title><title>BMC cancer</title><addtitle>BMC Cancer</addtitle><description>Vinca alkaloids are an important class of anticancer agents and semisynthetic vinca alkaloids are developed to improve the therapeutic index of this class of drugs. In the present study, a direct comparison was made between vinflunine and vinorelbine regarding their radiosensitizing and cell cycle effects.
Four human tumour cell lines were tested under identical experimental conditions, using equitoxic concentrations of vinflunine and vinorelbine.
Vinflunine and vinorelbine induced a comparable radiosensitizing effect (p-value never below 0.01) when cells were incubated for 24 h immediately prior to radiation. Regarding the cell cycle effects, a statistically significant concentration-dependent G2/M block was seen after 24 h incubation with vinorelbine in all tested cell lines. Similar results, with small cell line-related differences, were observed with vinflunine.
The radiosensitizing effects of both semisynthetic vinca alkaloids were comparable (not statistically different) and nearly always cell line-specific and concentration-dependent. The cell cycle effects could be related to the observed radiosensitizing effects. Considering the more favourable toxicity profile of vinflunine, this agent might be more promising than vinorelbine for chemoradiation studies in the clinic.</description><subject>Antineoplastic Agents, Phytogenic - chemistry</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>Breast Neoplasms - pathology</subject><subject>Carcinoma - pathology</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Cell Cycle - drug effects</subject><subject>Cell Line, Tumor - drug effects</subject><subject>Cell Line, Tumor - radiation effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Gamma Rays</subject><subject>Humans</subject><subject>Lung Neoplasms - pathology</subject><subject>Microtubules - drug effects</subject><subject>Molecular Structure</subject><subject>Radiation-Sensitizing Agents - pharmacology</subject><subject>Structure-Activity Relationship</subject><subject>Tongue Neoplasms - pathology</subject><subject>Urinary Bladder Neoplasms - pathology</subject><subject>Vinblastine - analogs & derivatives</subject><subject>Vinblastine - chemistry</subject><subject>Vinblastine - pharmacology</subject><issn>1471-2407</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNo9j0tLxDAUhYMgzji6dSn5AVZz27y2UnzBgJvZD2ly40TatDTpQP311ufq8B0-DhxCroDdAmh5B1xBUXKmCl1IcULW_8WKnKf0zhgozfQZWYGuoJRKrMmh7rvBjCaHI9KUJzfT3tN8QDoaF_qEMYUcPkJ8oyY6arFtqZ1tixS9R5vTl34M0bdTDBG_pQX7Edtm4Rsa4sJ57C_IqTdtwsvf3JDd48Oufi62r08v9f22GAQXRVU1EkB5o5yTyBt0JVotOW-kcI1EqdCW3mluLYCx0jLtjFHSSBQlKKg25PpndpiaDt1-GENnxnn_97j6BJafWFk</recordid><startdate>20080229</startdate><enddate>20080229</enddate><creator>Simoens, Cindy</creator><creator>Lardon, Filip</creator><creator>Pauwels, Bea</creator><creator>De Pooter, Christel M J</creator><creator>Lambrechts, Hilde A J</creator><creator>Pattyn, Greet G O</creator><creator>Breillout, Fabienne</creator><creator>Vermorken, Jan B</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20080229</creationdate><title>Comparative study of the radiosensitizing and cell cycle effects of vinflunine and vinorelbine, in vitro</title><author>Simoens, Cindy ; Lardon, Filip ; Pauwels, Bea ; De Pooter, Christel M J ; Lambrechts, Hilde A J ; Pattyn, Greet G O ; Breillout, Fabienne ; Vermorken, Jan B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p545-33b6117fa7dd6e4bed2ec8644b65db6e67ec2fd84cc11ac6c08daa76a6e521713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Antineoplastic Agents, Phytogenic - chemistry</topic><topic>Antineoplastic Agents, Phytogenic - pharmacology</topic><topic>Breast Neoplasms - pathology</topic><topic>Carcinoma - pathology</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Cell Cycle - drug effects</topic><topic>Cell Line, Tumor - drug effects</topic><topic>Cell Line, Tumor - radiation effects</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Gamma Rays</topic><topic>Humans</topic><topic>Lung Neoplasms - pathology</topic><topic>Microtubules - drug effects</topic><topic>Molecular Structure</topic><topic>Radiation-Sensitizing Agents - pharmacology</topic><topic>Structure-Activity Relationship</topic><topic>Tongue Neoplasms - pathology</topic><topic>Urinary Bladder Neoplasms - pathology</topic><topic>Vinblastine - analogs & derivatives</topic><topic>Vinblastine - chemistry</topic><topic>Vinblastine - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Simoens, Cindy</creatorcontrib><creatorcontrib>Lardon, Filip</creatorcontrib><creatorcontrib>Pauwels, Bea</creatorcontrib><creatorcontrib>De Pooter, Christel M J</creatorcontrib><creatorcontrib>Lambrechts, Hilde A J</creatorcontrib><creatorcontrib>Pattyn, Greet G O</creatorcontrib><creatorcontrib>Breillout, Fabienne</creatorcontrib><creatorcontrib>Vermorken, Jan B</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>BMC cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Simoens, Cindy</au><au>Lardon, Filip</au><au>Pauwels, Bea</au><au>De Pooter, Christel M J</au><au>Lambrechts, Hilde A J</au><au>Pattyn, Greet G O</au><au>Breillout, Fabienne</au><au>Vermorken, Jan B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative study of the radiosensitizing and cell cycle effects of vinflunine and vinorelbine, in vitro</atitle><jtitle>BMC cancer</jtitle><addtitle>BMC Cancer</addtitle><date>2008-02-29</date><risdate>2008</risdate><volume>8</volume><spage>65</spage><pages>65-</pages><eissn>1471-2407</eissn><abstract>Vinca alkaloids are an important class of anticancer agents and semisynthetic vinca alkaloids are developed to improve the therapeutic index of this class of drugs. In the present study, a direct comparison was made between vinflunine and vinorelbine regarding their radiosensitizing and cell cycle effects.
Four human tumour cell lines were tested under identical experimental conditions, using equitoxic concentrations of vinflunine and vinorelbine.
Vinflunine and vinorelbine induced a comparable radiosensitizing effect (p-value never below 0.01) when cells were incubated for 24 h immediately prior to radiation. Regarding the cell cycle effects, a statistically significant concentration-dependent G2/M block was seen after 24 h incubation with vinorelbine in all tested cell lines. Similar results, with small cell line-related differences, were observed with vinflunine.
The radiosensitizing effects of both semisynthetic vinca alkaloids were comparable (not statistically different) and nearly always cell line-specific and concentration-dependent. The cell cycle effects could be related to the observed radiosensitizing effects. Considering the more favourable toxicity profile of vinflunine, this agent might be more promising than vinorelbine for chemoradiation studies in the clinic.</abstract><cop>England</cop><pmid>18312675</pmid><doi>10.1186/1471-2407-8-65</doi></addata></record> |
fulltext | fulltext |
identifier | EISSN: 1471-2407 |
ispartof | BMC cancer, 2008-02, Vol.8, p.65 |
issn | 1471-2407 |
language | eng |
recordid | cdi_pubmed_primary_18312675 |
source | PubMed Central |
subjects | Antineoplastic Agents, Phytogenic - chemistry Antineoplastic Agents, Phytogenic - pharmacology Breast Neoplasms - pathology Carcinoma - pathology Carcinoma, Non-Small-Cell Lung - pathology Cell Cycle - drug effects Cell Line, Tumor - drug effects Cell Line, Tumor - radiation effects Dose-Response Relationship, Drug Female Gamma Rays Humans Lung Neoplasms - pathology Microtubules - drug effects Molecular Structure Radiation-Sensitizing Agents - pharmacology Structure-Activity Relationship Tongue Neoplasms - pathology Urinary Bladder Neoplasms - pathology Vinblastine - analogs & derivatives Vinblastine - chemistry Vinblastine - pharmacology |
title | Comparative study of the radiosensitizing and cell cycle effects of vinflunine and vinorelbine, in vitro |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T22%3A31%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Comparative%20study%20of%20the%20radiosensitizing%20and%20cell%20cycle%20effects%20of%20vinflunine%20and%20vinorelbine,%20in%20vitro&rft.jtitle=BMC%20cancer&rft.au=Simoens,%20Cindy&rft.date=2008-02-29&rft.volume=8&rft.spage=65&rft.pages=65-&rft.eissn=1471-2407&rft_id=info:doi/10.1186/1471-2407-8-65&rft_dat=%3Cpubmed%3E18312675%3C/pubmed%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-p545-33b6117fa7dd6e4bed2ec8644b65db6e67ec2fd84cc11ac6c08daa76a6e521713%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/18312675&rfr_iscdi=true |