Divergence between the high rate of p53 mutations in skin carcinomas and the low prevalence of anti-p53 antibodies
Circulating anti-p53 antibodies have been described and used as tumoural markers in patients with various cancers and strongly correlate with the p53 mutated status of the tumours. No study has yet looked at the prevalence of such antibodies in skin carcinoma patients although these tumours have bee...
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Veröffentlicht in: | British journal of cancer 2001-12, Vol.85 (12), p.1883-1886 |
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container_title | British journal of cancer |
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creator | Moch, C Moysan, A Lubin, R Salmonière, P de La Soufir, N Galisson, F Vilmer, C Venutolo, E Pelletier, F Le Janin, A Basset-Séguin, N |
description | Circulating anti-p53 antibodies have been described and used as tumoural markers in patients with various cancers and strongly correlate with the p53 mutated status of the tumours. No study has yet looked at the prevalence of such antibodies in skin carcinoma patients although these tumours have been shown to be frequently
p53
mutated. Most skin carcinoma can be diagnosed by examination or biopsy, but aggressive, recurrent and/or non-surgical cases’ follow up would be helped by a biological marker of residual disease. We performed a prospective study looking at the prevalence of anti-p53 antibodies using an ELISA technique in a series of 105 skin carcinoma patients in comparison with a sex- and age-matched control skin carcinoma-free group (
n
= 130). Additionally, p53 accumulation was studied by immunohistochemistry to confirm p53 protein altered expression in a sample of tumours. Anti-p53 antibodies were detected in 2.9% of the cases, with a higher prevalence in patients suffering from the more aggressive squamous cell type (SCC) of skin carcinoma (8%) than for the more common and slowly growing basal cell carcinoma type or BCC (1.5%). p53 protein stabilization could be confirmed in 80% of tumours studied by IHC. This low level of anti-p53 antibody detection contrasts with the high rate of p53 mutations reported in these tumours. This observation shows that the anti-p53 humoral response is a complex and tissue-specific mechanism. © 2001 Cancer Research Campaign
http://www.bjcancer.com |
doi_str_mv | 10.1054/bjoc.2001.2185 |
format | Article |
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p53
mutated. Most skin carcinoma can be diagnosed by examination or biopsy, but aggressive, recurrent and/or non-surgical cases’ follow up would be helped by a biological marker of residual disease. We performed a prospective study looking at the prevalence of anti-p53 antibodies using an ELISA technique in a series of 105 skin carcinoma patients in comparison with a sex- and age-matched control skin carcinoma-free group (
n
= 130). Additionally, p53 accumulation was studied by immunohistochemistry to confirm p53 protein altered expression in a sample of tumours. Anti-p53 antibodies were detected in 2.9% of the cases, with a higher prevalence in patients suffering from the more aggressive squamous cell type (SCC) of skin carcinoma (8%) than for the more common and slowly growing basal cell carcinoma type or BCC (1.5%). p53 protein stabilization could be confirmed in 80% of tumours studied by IHC. This low level of anti-p53 antibody detection contrasts with the high rate of p53 mutations reported in these tumours. This observation shows that the anti-p53 humoral response is a complex and tissue-specific mechanism. © 2001 Cancer Research Campaign
http://www.bjcancer.com</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1054/bjoc.2001.2185</identifier><identifier>PMID: 11747330</identifier><identifier>CODEN: BJCAAI</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antibody Specificity ; Autoantibodies - blood ; Autoantibodies - immunology ; Biological and medical sciences ; Biomarkers, Tumor - analysis ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Carcinoma, Basal Cell - blood ; Carcinoma, Basal Cell - genetics ; Carcinoma, Basal Cell - immunology ; Carcinoma, Basal Cell - pathology ; Carcinoma, Squamous Cell - blood ; Carcinoma, Squamous Cell - genetics ; Carcinoma, Squamous Cell - immunology ; Carcinoma, Squamous Cell - pathology ; Case-Control Studies ; Dermatology ; Drug Resistance ; Enzyme-Linked Immunosorbent Assay ; Epidemiology ; Female ; Genes, p53 ; Humans ; Immunologic Deficiency Syndromes - etiology ; Male ; Medical sciences ; Middle Aged ; Molecular Medicine ; Neoplasm Proteins - immunology ; Neoplasms, Radiation-Induced - blood ; Neoplasms, Radiation-Induced - genetics ; Neoplasms, Radiation-Induced - immunology ; Neoplasms, Radiation-Induced - pathology ; Oncology ; Prospective Studies ; Regular ; regular-article ; skin carcinoma ; Skin Diseases - blood ; Skin Diseases - genetics ; Skin Diseases - immunology ; Skin Diseases - pathology ; Skin Neoplasms - blood ; Skin Neoplasms - genetics ; Skin Neoplasms - immunology ; Skin Neoplasms - pathology ; Tumor Suppressor Protein p53 - immunology ; Tumors of the skin and soft tissue. Premalignant lesions ; Ultraviolet Rays - adverse effects</subject><ispartof>British journal of cancer, 2001-12, Vol.85 (12), p.1883-1886</ispartof><rights>The Author(s) 2001</rights><rights>2002 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Dec 2001</rights><rights>Copyright © 2001 Cancer Research Campaign 2001 Cancer Research Campaign</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c663t-85c98468566c188b82f801e3ca135e71c2ea1cc2d70b808283f9c6703a0f31e03</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364020/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364020/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,2727,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13421960$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11747330$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moch, C</creatorcontrib><creatorcontrib>Moysan, A</creatorcontrib><creatorcontrib>Lubin, R</creatorcontrib><creatorcontrib>Salmonière, P de La</creatorcontrib><creatorcontrib>Soufir, N</creatorcontrib><creatorcontrib>Galisson, F</creatorcontrib><creatorcontrib>Vilmer, C</creatorcontrib><creatorcontrib>Venutolo, E</creatorcontrib><creatorcontrib>Pelletier, F Le</creatorcontrib><creatorcontrib>Janin, A</creatorcontrib><creatorcontrib>Basset-Séguin, N</creatorcontrib><title>Divergence between the high rate of p53 mutations in skin carcinomas and the low prevalence of anti-p53 antibodies</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><addtitle>Br J Cancer</addtitle><description>Circulating anti-p53 antibodies have been described and used as tumoural markers in patients with various cancers and strongly correlate with the p53 mutated status of the tumours. No study has yet looked at the prevalence of such antibodies in skin carcinoma patients although these tumours have been shown to be frequently
p53
mutated. Most skin carcinoma can be diagnosed by examination or biopsy, but aggressive, recurrent and/or non-surgical cases’ follow up would be helped by a biological marker of residual disease. We performed a prospective study looking at the prevalence of anti-p53 antibodies using an ELISA technique in a series of 105 skin carcinoma patients in comparison with a sex- and age-matched control skin carcinoma-free group (
n
= 130). Additionally, p53 accumulation was studied by immunohistochemistry to confirm p53 protein altered expression in a sample of tumours. Anti-p53 antibodies were detected in 2.9% of the cases, with a higher prevalence in patients suffering from the more aggressive squamous cell type (SCC) of skin carcinoma (8%) than for the more common and slowly growing basal cell carcinoma type or BCC (1.5%). p53 protein stabilization could be confirmed in 80% of tumours studied by IHC. This low level of anti-p53 antibody detection contrasts with the high rate of p53 mutations reported in these tumours. This observation shows that the anti-p53 humoral response is a complex and tissue-specific mechanism. © 2001 Cancer Research Campaign
http://www.bjcancer.com</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antibody Specificity</subject><subject>Autoantibodies - blood</subject><subject>Autoantibodies - immunology</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Carcinoma, Basal Cell - blood</subject><subject>Carcinoma, Basal Cell - genetics</subject><subject>Carcinoma, Basal Cell - immunology</subject><subject>Carcinoma, Basal Cell - pathology</subject><subject>Carcinoma, Squamous Cell - blood</subject><subject>Carcinoma, Squamous Cell - genetics</subject><subject>Carcinoma, Squamous Cell - immunology</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Case-Control Studies</subject><subject>Dermatology</subject><subject>Drug Resistance</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Genes, p53</subject><subject>Humans</subject><subject>Immunologic Deficiency Syndromes - etiology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Molecular Medicine</subject><subject>Neoplasm Proteins - immunology</subject><subject>Neoplasms, Radiation-Induced - blood</subject><subject>Neoplasms, Radiation-Induced - genetics</subject><subject>Neoplasms, Radiation-Induced - immunology</subject><subject>Neoplasms, Radiation-Induced - pathology</subject><subject>Oncology</subject><subject>Prospective Studies</subject><subject>Regular</subject><subject>regular-article</subject><subject>skin carcinoma</subject><subject>Skin Diseases - blood</subject><subject>Skin Diseases - genetics</subject><subject>Skin Diseases - immunology</subject><subject>Skin Diseases - pathology</subject><subject>Skin Neoplasms - blood</subject><subject>Skin Neoplasms - genetics</subject><subject>Skin Neoplasms - immunology</subject><subject>Skin Neoplasms - pathology</subject><subject>Tumor Suppressor Protein p53 - immunology</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><subject>Ultraviolet Rays - adverse effects</subject><issn>0007-0920</issn><issn>1532-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kc2P0zAQxS0EYsvClRvIQgJO6Y7txHEuSGj5lFbiAmfLcSetS2IXO-mK_x6nrbaABBd_aH7vzdiPkKcMlgyq8qrdBrvkAGzJmarukQWrBC-Y4vV9sgCAuoCGwwV5lNI2XxtQ9UNywVhd1kLAgsR3bo9xjd4ibXG8RfR03CDduPWGRjMiDR3dVYIO02hGF3yiztP0PS_WROt8GEyixq8Oqj7c0l3EvekPhllq_OiKWT8f2rBymB6TB53pEz457Zfk24f3X68_FTdfPn6-fntTWCnFWKjKNqqUqpLSMqVaxTsFDIU1TFRYM8vRMGv5qoZWgeJKdI2VNQgDnWAI4pK8OfrupnbAlUU_RtPrXXSDiT91ME7_WfFuo9dhr7mQJfDZ4PXJIIYfE6ZRDy5Z7HvjMUxJK6h5XTWNyuSr_5I5j6qUMFu--Avchin6_A2a8-xUMtVkaHmEbAwpRezuZmag59T1nLqeU9dz6lnw_PeXnvFTzBl4eQJMsqbvovHWpTMnSs4aOXNXRy7lkl9jPI_3z9bPjgpvxininaWUzaH-C2Rfzmk</recordid><startdate>20011214</startdate><enddate>20011214</enddate><creator>Moch, C</creator><creator>Moysan, A</creator><creator>Lubin, R</creator><creator>Salmonière, P de La</creator><creator>Soufir, N</creator><creator>Galisson, F</creator><creator>Vilmer, C</creator><creator>Venutolo, E</creator><creator>Pelletier, F Le</creator><creator>Janin, A</creator><creator>Basset-Séguin, N</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><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><scope>3V.</scope><scope>7RV</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7U7</scope><scope>C1K</scope><scope>5PM</scope></search><sort><creationdate>20011214</creationdate><title>Divergence between the high rate of p53 mutations in skin carcinomas and the low prevalence of anti-p53 antibodies</title><author>Moch, C ; Moysan, A ; Lubin, R ; Salmonière, P de La ; Soufir, N ; Galisson, F ; Vilmer, C ; Venutolo, E ; Pelletier, F Le ; Janin, A ; Basset-Séguin, N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c663t-85c98468566c188b82f801e3ca135e71c2ea1cc2d70b808283f9c6703a0f31e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antibody Specificity</topic><topic>Autoantibodies - blood</topic><topic>Autoantibodies - immunology</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Carcinoma, Basal Cell - blood</topic><topic>Carcinoma, Basal Cell - genetics</topic><topic>Carcinoma, Basal Cell - immunology</topic><topic>Carcinoma, Basal Cell - pathology</topic><topic>Carcinoma, Squamous Cell - blood</topic><topic>Carcinoma, Squamous Cell - genetics</topic><topic>Carcinoma, Squamous Cell - immunology</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Case-Control Studies</topic><topic>Dermatology</topic><topic>Drug Resistance</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Epidemiology</topic><topic>Female</topic><topic>Genes, p53</topic><topic>Humans</topic><topic>Immunologic Deficiency Syndromes - etiology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Molecular Medicine</topic><topic>Neoplasm Proteins - immunology</topic><topic>Neoplasms, Radiation-Induced - blood</topic><topic>Neoplasms, Radiation-Induced - genetics</topic><topic>Neoplasms, Radiation-Induced - immunology</topic><topic>Neoplasms, Radiation-Induced - pathology</topic><topic>Oncology</topic><topic>Prospective Studies</topic><topic>Regular</topic><topic>regular-article</topic><topic>skin carcinoma</topic><topic>Skin Diseases - blood</topic><topic>Skin Diseases - genetics</topic><topic>Skin Diseases - immunology</topic><topic>Skin Diseases - pathology</topic><topic>Skin Neoplasms - blood</topic><topic>Skin Neoplasms - genetics</topic><topic>Skin Neoplasms - immunology</topic><topic>Skin Neoplasms - pathology</topic><topic>Tumor Suppressor Protein p53 - immunology</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><topic>Ultraviolet Rays - adverse effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moch, C</creatorcontrib><creatorcontrib>Moysan, A</creatorcontrib><creatorcontrib>Lubin, R</creatorcontrib><creatorcontrib>Salmonière, P de La</creatorcontrib><creatorcontrib>Soufir, N</creatorcontrib><creatorcontrib>Galisson, F</creatorcontrib><creatorcontrib>Vilmer, C</creatorcontrib><creatorcontrib>Venutolo, E</creatorcontrib><creatorcontrib>Pelletier, F Le</creatorcontrib><creatorcontrib>Janin, A</creatorcontrib><creatorcontrib>Basset-Séguin, N</creatorcontrib><collection>Springer Nature OA Free Journals</collection><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><collection>ProQuest Central (Corporate)</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health 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>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</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 Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moch, C</au><au>Moysan, A</au><au>Lubin, R</au><au>Salmonière, P de La</au><au>Soufir, N</au><au>Galisson, F</au><au>Vilmer, C</au><au>Venutolo, E</au><au>Pelletier, F Le</au><au>Janin, A</au><au>Basset-Séguin, N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Divergence between the high rate of p53 mutations in skin carcinomas and the low prevalence of anti-p53 antibodies</atitle><jtitle>British journal of cancer</jtitle><stitle>Br J Cancer</stitle><addtitle>Br J Cancer</addtitle><date>2001-12-14</date><risdate>2001</risdate><volume>85</volume><issue>12</issue><spage>1883</spage><epage>1886</epage><pages>1883-1886</pages><issn>0007-0920</issn><eissn>1532-1827</eissn><coden>BJCAAI</coden><abstract>Circulating anti-p53 antibodies have been described and used as tumoural markers in patients with various cancers and strongly correlate with the p53 mutated status of the tumours. No study has yet looked at the prevalence of such antibodies in skin carcinoma patients although these tumours have been shown to be frequently
p53
mutated. Most skin carcinoma can be diagnosed by examination or biopsy, but aggressive, recurrent and/or non-surgical cases’ follow up would be helped by a biological marker of residual disease. We performed a prospective study looking at the prevalence of anti-p53 antibodies using an ELISA technique in a series of 105 skin carcinoma patients in comparison with a sex- and age-matched control skin carcinoma-free group (
n
= 130). Additionally, p53 accumulation was studied by immunohistochemistry to confirm p53 protein altered expression in a sample of tumours. Anti-p53 antibodies were detected in 2.9% of the cases, with a higher prevalence in patients suffering from the more aggressive squamous cell type (SCC) of skin carcinoma (8%) than for the more common and slowly growing basal cell carcinoma type or BCC (1.5%). p53 protein stabilization could be confirmed in 80% of tumours studied by IHC. This low level of anti-p53 antibody detection contrasts with the high rate of p53 mutations reported in these tumours. This observation shows that the anti-p53 humoral response is a complex and tissue-specific mechanism. © 2001 Cancer Research Campaign
http://www.bjcancer.com</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>11747330</pmid><doi>10.1054/bjoc.2001.2185</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Aged, 80 and over Antibody Specificity Autoantibodies - blood Autoantibodies - immunology Biological and medical sciences Biomarkers, Tumor - analysis Biomedical and Life Sciences Biomedicine Cancer Research Carcinoma, Basal Cell - blood Carcinoma, Basal Cell - genetics Carcinoma, Basal Cell - immunology Carcinoma, Basal Cell - pathology Carcinoma, Squamous Cell - blood Carcinoma, Squamous Cell - genetics Carcinoma, Squamous Cell - immunology Carcinoma, Squamous Cell - pathology Case-Control Studies Dermatology Drug Resistance Enzyme-Linked Immunosorbent Assay Epidemiology Female Genes, p53 Humans Immunologic Deficiency Syndromes - etiology Male Medical sciences Middle Aged Molecular Medicine Neoplasm Proteins - immunology Neoplasms, Radiation-Induced - blood Neoplasms, Radiation-Induced - genetics Neoplasms, Radiation-Induced - immunology Neoplasms, Radiation-Induced - pathology Oncology Prospective Studies Regular regular-article skin carcinoma Skin Diseases - blood Skin Diseases - genetics Skin Diseases - immunology Skin Diseases - pathology Skin Neoplasms - blood Skin Neoplasms - genetics Skin Neoplasms - immunology Skin Neoplasms - pathology Tumor Suppressor Protein p53 - immunology Tumors of the skin and soft tissue. Premalignant lesions Ultraviolet Rays - adverse effects |
title | Divergence between the high rate of p53 mutations in skin carcinomas and the low prevalence of anti-p53 antibodies |
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