Reactive oxygen species and melanoma: an explanation for gender differences in survival?

Summary Epidemiological research consistently shows a female advantage in melanoma survival. So far, no definite candidate for the explanation of this phenomenon has emerged. We propose that gender differences in oxidative stress caused by radical oxygen species (ROS) underlie these survival differe...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Pigment cell and melanoma research 2010-06, Vol.23 (3), p.352-364
Hauptverfasser: Joosse, Arjen, De Vries, Esther, Van Eijck, Casper H., Eggermont, Alexander M. M., Nijsten, Tamar, Coebergh, Jan Willem W.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 364
container_issue 3
container_start_page 352
container_title Pigment cell and melanoma research
container_volume 23
creator Joosse, Arjen
De Vries, Esther
Van Eijck, Casper H.
Eggermont, Alexander M. M.
Nijsten, Tamar
Coebergh, Jan Willem W.
description Summary Epidemiological research consistently shows a female advantage in melanoma survival. So far, no definite candidate for the explanation of this phenomenon has emerged. We propose that gender differences in oxidative stress caused by radical oxygen species (ROS) underlie these survival differences. It is known that males express lower amounts of anti‐oxidant enzymes, resulting in more oxidative stress than females. The primary melanoma environment is characterized by high ROS levels, from exogenous sources as well as ROS production within melanoma cells themselves. ROS are known to be able to promote metastasis through a wide variety of mechanisms. We hypothesize that the higher levels of ROS in men enhance selection of ROS‐resistance in melanoma cells. Subsequently, ROS can stimulate the metastatic potential of melanoma cells. In addition, due to the lower anti‐oxidant defenses in men, ROS produced by melanoma cells cause more damage to healthy tissues surrounding the tumor, further stimulating metastasis. Therefore, ROS may explain the observed differences between males and females in melanoma survival.
doi_str_mv 10.1111/j.1755-148X.2010.00694.x
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_733139603</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>733139603</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4564-9b3aeef17e03aa847ee620e18381d04ef16c7688cb656d672730c28005f396313</originalsourceid><addsrcrecordid>eNqNkMtOAyEUhonReKm-gmHnaioMM8CYGGMarSZVm0Zjd4QyZwx1LhXaOn17qa1dywYO5_sO5EcIU9KlYV1Ou1SkaUQTOe7GJNwSwrOk2-6h411jf3cW9AideD8NEEkzdoiOYhJTmUl6jMYj0GZul4CbdvUBNfYzMBY81nWOKyh13VT6KlQY2lmo9Nw2NS4ahwOcg8O5LQpwUJvg2KAv3NIudXlzig4KXXo42-4d9HZ_99p7iAYv_cfe7SAyScqTKJswDVBQAYRpLRMBwGMCVDJJc5KEDjeCS2kmPOU5F7FgxMSSkLRgGWeUddDFZu7MNV8L8HNVWW-gDH-FZuGVYAHKOGGBlBvSuMZ7B4WaOVtpt1KUqHWsaqrWial1emodq_qNVbVBPd8-sphUkO_EvxwDcL0Bvm0Jq38PVsPe0yicgh9tfOvn0O587T4VF0yk6v25r_rZKOun8VD12A-9pZV0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>733139603</pqid></control><display><type>article</type><title>Reactive oxygen species and melanoma: an explanation for gender differences in survival?</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>Joosse, Arjen ; De Vries, Esther ; Van Eijck, Casper H. ; Eggermont, Alexander M. M. ; Nijsten, Tamar ; Coebergh, Jan Willem W.</creator><creatorcontrib>Joosse, Arjen ; De Vries, Esther ; Van Eijck, Casper H. ; Eggermont, Alexander M. M. ; Nijsten, Tamar ; Coebergh, Jan Willem W.</creatorcontrib><description>Summary Epidemiological research consistently shows a female advantage in melanoma survival. So far, no definite candidate for the explanation of this phenomenon has emerged. We propose that gender differences in oxidative stress caused by radical oxygen species (ROS) underlie these survival differences. It is known that males express lower amounts of anti‐oxidant enzymes, resulting in more oxidative stress than females. The primary melanoma environment is characterized by high ROS levels, from exogenous sources as well as ROS production within melanoma cells themselves. ROS are known to be able to promote metastasis through a wide variety of mechanisms. We hypothesize that the higher levels of ROS in men enhance selection of ROS‐resistance in melanoma cells. Subsequently, ROS can stimulate the metastatic potential of melanoma cells. In addition, due to the lower anti‐oxidant defenses in men, ROS produced by melanoma cells cause more damage to healthy tissues surrounding the tumor, further stimulating metastasis. Therefore, ROS may explain the observed differences between males and females in melanoma survival.</description><identifier>ISSN: 1755-1471</identifier><identifier>EISSN: 1755-148X</identifier><identifier>DOI: 10.1111/j.1755-148X.2010.00694.x</identifier><identifier>PMID: 20218981</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>anti-oxidants ; Antioxidants - metabolism ; Female ; gender differences ; Humans ; Male ; melanoma ; Melanoma - metabolism ; Melanoma - pathology ; metastasis ; Models, Biological ; Oxidative Stress ; reactive oxygen species ; Reactive Oxygen Species - metabolism ; Sex Characteristics ; Skin Neoplasms - metabolism ; Skin Neoplasms - pathology ; survival ; Survival Analysis</subject><ispartof>Pigment cell and melanoma research, 2010-06, Vol.23 (3), p.352-364</ispartof><rights>2010 John Wiley &amp; Sons A/S</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4564-9b3aeef17e03aa847ee620e18381d04ef16c7688cb656d672730c28005f396313</citedby><cites>FETCH-LOGICAL-c4564-9b3aeef17e03aa847ee620e18381d04ef16c7688cb656d672730c28005f396313</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1755-148X.2010.00694.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1755-148X.2010.00694.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20218981$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Joosse, Arjen</creatorcontrib><creatorcontrib>De Vries, Esther</creatorcontrib><creatorcontrib>Van Eijck, Casper H.</creatorcontrib><creatorcontrib>Eggermont, Alexander M. M.</creatorcontrib><creatorcontrib>Nijsten, Tamar</creatorcontrib><creatorcontrib>Coebergh, Jan Willem W.</creatorcontrib><title>Reactive oxygen species and melanoma: an explanation for gender differences in survival?</title><title>Pigment cell and melanoma research</title><addtitle>Pigment Cell Melanoma Res</addtitle><description>Summary Epidemiological research consistently shows a female advantage in melanoma survival. So far, no definite candidate for the explanation of this phenomenon has emerged. We propose that gender differences in oxidative stress caused by radical oxygen species (ROS) underlie these survival differences. It is known that males express lower amounts of anti‐oxidant enzymes, resulting in more oxidative stress than females. The primary melanoma environment is characterized by high ROS levels, from exogenous sources as well as ROS production within melanoma cells themselves. ROS are known to be able to promote metastasis through a wide variety of mechanisms. We hypothesize that the higher levels of ROS in men enhance selection of ROS‐resistance in melanoma cells. Subsequently, ROS can stimulate the metastatic potential of melanoma cells. In addition, due to the lower anti‐oxidant defenses in men, ROS produced by melanoma cells cause more damage to healthy tissues surrounding the tumor, further stimulating metastasis. Therefore, ROS may explain the observed differences between males and females in melanoma survival.</description><subject>anti-oxidants</subject><subject>Antioxidants - metabolism</subject><subject>Female</subject><subject>gender differences</subject><subject>Humans</subject><subject>Male</subject><subject>melanoma</subject><subject>Melanoma - metabolism</subject><subject>Melanoma - pathology</subject><subject>metastasis</subject><subject>Models, Biological</subject><subject>Oxidative Stress</subject><subject>reactive oxygen species</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Sex Characteristics</subject><subject>Skin Neoplasms - metabolism</subject><subject>Skin Neoplasms - pathology</subject><subject>survival</subject><subject>Survival Analysis</subject><issn>1755-1471</issn><issn>1755-148X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMtOAyEUhonReKm-gmHnaioMM8CYGGMarSZVm0Zjd4QyZwx1LhXaOn17qa1dywYO5_sO5EcIU9KlYV1Ou1SkaUQTOe7GJNwSwrOk2-6h411jf3cW9AideD8NEEkzdoiOYhJTmUl6jMYj0GZul4CbdvUBNfYzMBY81nWOKyh13VT6KlQY2lmo9Nw2NS4ahwOcg8O5LQpwUJvg2KAv3NIudXlzig4KXXo42-4d9HZ_99p7iAYv_cfe7SAyScqTKJswDVBQAYRpLRMBwGMCVDJJc5KEDjeCS2kmPOU5F7FgxMSSkLRgGWeUddDFZu7MNV8L8HNVWW-gDH-FZuGVYAHKOGGBlBvSuMZ7B4WaOVtpt1KUqHWsaqrWial1emodq_qNVbVBPd8-sphUkO_EvxwDcL0Bvm0Jq38PVsPe0yicgh9tfOvn0O587T4VF0yk6v25r_rZKOun8VD12A-9pZV0</recordid><startdate>201006</startdate><enddate>201006</enddate><creator>Joosse, Arjen</creator><creator>De Vries, Esther</creator><creator>Van Eijck, Casper H.</creator><creator>Eggermont, Alexander M. M.</creator><creator>Nijsten, Tamar</creator><creator>Coebergh, Jan Willem W.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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><scope>7X8</scope></search><sort><creationdate>201006</creationdate><title>Reactive oxygen species and melanoma: an explanation for gender differences in survival?</title><author>Joosse, Arjen ; De Vries, Esther ; Van Eijck, Casper H. ; Eggermont, Alexander M. M. ; Nijsten, Tamar ; Coebergh, Jan Willem W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4564-9b3aeef17e03aa847ee620e18381d04ef16c7688cb656d672730c28005f396313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>anti-oxidants</topic><topic>Antioxidants - metabolism</topic><topic>Female</topic><topic>gender differences</topic><topic>Humans</topic><topic>Male</topic><topic>melanoma</topic><topic>Melanoma - metabolism</topic><topic>Melanoma - pathology</topic><topic>metastasis</topic><topic>Models, Biological</topic><topic>Oxidative Stress</topic><topic>reactive oxygen species</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Sex Characteristics</topic><topic>Skin Neoplasms - metabolism</topic><topic>Skin Neoplasms - pathology</topic><topic>survival</topic><topic>Survival Analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Joosse, Arjen</creatorcontrib><creatorcontrib>De Vries, Esther</creatorcontrib><creatorcontrib>Van Eijck, Casper H.</creatorcontrib><creatorcontrib>Eggermont, Alexander M. M.</creatorcontrib><creatorcontrib>Nijsten, Tamar</creatorcontrib><creatorcontrib>Coebergh, Jan Willem W.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Pigment cell and melanoma research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Joosse, Arjen</au><au>De Vries, Esther</au><au>Van Eijck, Casper H.</au><au>Eggermont, Alexander M. M.</au><au>Nijsten, Tamar</au><au>Coebergh, Jan Willem W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reactive oxygen species and melanoma: an explanation for gender differences in survival?</atitle><jtitle>Pigment cell and melanoma research</jtitle><addtitle>Pigment Cell Melanoma Res</addtitle><date>2010-06</date><risdate>2010</risdate><volume>23</volume><issue>3</issue><spage>352</spage><epage>364</epage><pages>352-364</pages><issn>1755-1471</issn><eissn>1755-148X</eissn><abstract>Summary Epidemiological research consistently shows a female advantage in melanoma survival. So far, no definite candidate for the explanation of this phenomenon has emerged. We propose that gender differences in oxidative stress caused by radical oxygen species (ROS) underlie these survival differences. It is known that males express lower amounts of anti‐oxidant enzymes, resulting in more oxidative stress than females. The primary melanoma environment is characterized by high ROS levels, from exogenous sources as well as ROS production within melanoma cells themselves. ROS are known to be able to promote metastasis through a wide variety of mechanisms. We hypothesize that the higher levels of ROS in men enhance selection of ROS‐resistance in melanoma cells. Subsequently, ROS can stimulate the metastatic potential of melanoma cells. In addition, due to the lower anti‐oxidant defenses in men, ROS produced by melanoma cells cause more damage to healthy tissues surrounding the tumor, further stimulating metastasis. Therefore, ROS may explain the observed differences between males and females in melanoma survival.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>20218981</pmid><doi>10.1111/j.1755-148X.2010.00694.x</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1755-1471
ispartof Pigment cell and melanoma research, 2010-06, Vol.23 (3), p.352-364
issn 1755-1471
1755-148X
language eng
recordid cdi_proquest_miscellaneous_733139603
source MEDLINE; Access via Wiley Online Library
subjects anti-oxidants
Antioxidants - metabolism
Female
gender differences
Humans
Male
melanoma
Melanoma - metabolism
Melanoma - pathology
metastasis
Models, Biological
Oxidative Stress
reactive oxygen species
Reactive Oxygen Species - metabolism
Sex Characteristics
Skin Neoplasms - metabolism
Skin Neoplasms - pathology
survival
Survival Analysis
title Reactive oxygen species and melanoma: an explanation for gender differences in survival?
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-23T12%3A27%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Reactive%20oxygen%20species%20and%20melanoma:%20an%20explanation%20for%20gender%20differences%20in%20survival?&rft.jtitle=Pigment%20cell%20and%20melanoma%20research&rft.au=Joosse,%20Arjen&rft.date=2010-06&rft.volume=23&rft.issue=3&rft.spage=352&rft.epage=364&rft.pages=352-364&rft.issn=1755-1471&rft.eissn=1755-148X&rft_id=info:doi/10.1111/j.1755-148X.2010.00694.x&rft_dat=%3Cproquest_cross%3E733139603%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=733139603&rft_id=info:pmid/20218981&rfr_iscdi=true