Loading…

Expression of p73 in normal skin and proliferative skin lesions

The p73 gene is a member of the p53 gene family and the structure and functions of p73 protein are similar to those of  p53.  However,  these  two  proteins  have  different  roles. In the present study, p73 protein was found immunohistochemically to be distributed in the basal cells of the epidermi...

Full description

Saved in:
Bibliographic Details
Published in:Pathology international 2004-12, Vol.54 (12), p.890-895
Main Authors: Kamiya, Makoto, Takeuchi, Yuko, Katho, Mari, Yokoo, Hideaki, Sasaki, Atsushi, Nakazato, Yoichi
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-c5557-a688fc8ba2e69cc50b3dff1c842164de6a9f2093ed585ca9f5b8e82708dccfd43
cites cdi_FETCH-LOGICAL-c5557-a688fc8ba2e69cc50b3dff1c842164de6a9f2093ed585ca9f5b8e82708dccfd43
container_end_page 895
container_issue 12
container_start_page 890
container_title Pathology international
container_volume 54
creator Kamiya, Makoto
Takeuchi, Yuko
Katho, Mari
Yokoo, Hideaki
Sasaki, Atsushi
Nakazato, Yoichi
description The p73 gene is a member of the p53 gene family and the structure and functions of p73 protein are similar to those of  p53.  However,  these  two  proteins  have  different  roles. In the present study, p73 protein was found immunohistochemically to be distributed in the basal cells of the epidermis, columnar basal cells in the hair follicle and peripheral cells without lipid droplets in the sebaceous and meibomian glands; it was expressed strongly in tumor cells in basal cell carcinomas and in the basal cell‐like cells in seborrheic keratosis, and weakly or negatively in the squamous cell‐like cells in seborrheic keratosis and in the tumor cells in squamous cell carcinomas. No relationship was detected between p73 and p53 protein distribution and between p73 protein expression and the proliferative potential, as shown by the Ki‐67 immunopositive cell ratio. The present study shows that p73 protein is likely to play important roles in skin differentiation rather than proliferation or carcinogenesis of the skin.
doi_str_mv 10.1111/j.1440-1827.2004.01777.x
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_19416048</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>19416048</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5557-a688fc8ba2e69cc50b3dff1c842164de6a9f2093ed585ca9f5b8e82708dccfd43</originalsourceid><addsrcrecordid>eNqNkEFPwyAYhonRuDn9C6Ynb61QoNCDMTrntrhMEzUeCaWQdOvaCZt2_15ql3mVCx_wPh_wABAgGCE_rhcRIgSGiMcsiiEkEUSMsag5Av3DwbGvcQxDShLcA2fOLaBP4QSegh6iNOUYwT64HTVrq50r6iqoTbBmOCiqoKrtSpaBW_paVnmwtnVZGG3lpvjS3XapW8adgxMjS6cv9vMAvD-O3oaTcPY8ng7vZqGilLJQJpwbxTMZ6yRVisIM58YgxUmMEpLrRKYmhinWOeVU-QXNuPafgDxXyuQED8BV19c_5XOr3UasCqd0WcpK11snUEpQAgn3Qd4Fla2ds9qItS1W0u4EgqKVJxaidSRaR6KVJ37licajl_s7ttlK53_g3pYP3HSB76LUu383Fi_TeVt5Puz4wm10c-ClXYqEYUbFx3wsnl7ZeILuHwTFP5oUjJg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>19416048</pqid></control><display><type>article</type><title>Expression of p73 in normal skin and proliferative skin lesions</title><source>Wiley</source><creator>Kamiya, Makoto ; Takeuchi, Yuko ; Katho, Mari ; Yokoo, Hideaki ; Sasaki, Atsushi ; Nakazato, Yoichi</creator><creatorcontrib>Kamiya, Makoto ; Takeuchi, Yuko ; Katho, Mari ; Yokoo, Hideaki ; Sasaki, Atsushi ; Nakazato, Yoichi</creatorcontrib><description>The p73 gene is a member of the p53 gene family and the structure and functions of p73 protein are similar to those of  p53.  However,  these  two  proteins  have  different  roles. In the present study, p73 protein was found immunohistochemically to be distributed in the basal cells of the epidermis, columnar basal cells in the hair follicle and peripheral cells without lipid droplets in the sebaceous and meibomian glands; it was expressed strongly in tumor cells in basal cell carcinomas and in the basal cell‐like cells in seborrheic keratosis, and weakly or negatively in the squamous cell‐like cells in seborrheic keratosis and in the tumor cells in squamous cell carcinomas. No relationship was detected between p73 and p53 protein distribution and between p73 protein expression and the proliferative potential, as shown by the Ki‐67 immunopositive cell ratio. The present study shows that p73 protein is likely to play important roles in skin differentiation rather than proliferation or carcinogenesis of the skin.</description><identifier>ISSN: 1320-5463</identifier><identifier>EISSN: 1440-1827</identifier><identifier>DOI: 10.1111/j.1440-1827.2004.01777.x</identifier><identifier>PMID: 15598310</identifier><language>eng</language><publisher>Melbourne, Australia: Blackwell Science Pty</publisher><subject>Biomarkers, Tumor - analysis ; carcinogenesis ; Carcinoma, Basal Cell - metabolism ; Carcinoma, Basal Cell - pathology ; Cell Proliferation ; differentiation ; DNA-Binding Proteins - biosynthesis ; Genes, Tumor Suppressor ; Humans ; Immunohistochemistry ; Keratosis, Seborrheic - metabolism ; Keratosis, Seborrheic - pathology ; Ki-67 Antigen - metabolism ; Neoplasms, Squamous Cell - metabolism ; Neoplasms, Squamous Cell - pathology ; Nuclear Proteins - biosynthesis ; p53 ; p73 ; skin ; Skin - metabolism ; Skin Diseases - metabolism ; Skin Diseases - pathology ; Skin Neoplasms - metabolism ; Skin Neoplasms - pathology ; Tumor Protein p73 ; Tumor Suppressor Protein p53 - biosynthesis ; Tumor Suppressor Proteins</subject><ispartof>Pathology international, 2004-12, Vol.54 (12), p.890-895</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5557-a688fc8ba2e69cc50b3dff1c842164de6a9f2093ed585ca9f5b8e82708dccfd43</citedby><cites>FETCH-LOGICAL-c5557-a688fc8ba2e69cc50b3dff1c842164de6a9f2093ed585ca9f5b8e82708dccfd43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15598310$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kamiya, Makoto</creatorcontrib><creatorcontrib>Takeuchi, Yuko</creatorcontrib><creatorcontrib>Katho, Mari</creatorcontrib><creatorcontrib>Yokoo, Hideaki</creatorcontrib><creatorcontrib>Sasaki, Atsushi</creatorcontrib><creatorcontrib>Nakazato, Yoichi</creatorcontrib><title>Expression of p73 in normal skin and proliferative skin lesions</title><title>Pathology international</title><addtitle>Pathol Int</addtitle><description>The p73 gene is a member of the p53 gene family and the structure and functions of p73 protein are similar to those of  p53.  However,  these  two  proteins  have  different  roles. In the present study, p73 protein was found immunohistochemically to be distributed in the basal cells of the epidermis, columnar basal cells in the hair follicle and peripheral cells without lipid droplets in the sebaceous and meibomian glands; it was expressed strongly in tumor cells in basal cell carcinomas and in the basal cell‐like cells in seborrheic keratosis, and weakly or negatively in the squamous cell‐like cells in seborrheic keratosis and in the tumor cells in squamous cell carcinomas. No relationship was detected between p73 and p53 protein distribution and between p73 protein expression and the proliferative potential, as shown by the Ki‐67 immunopositive cell ratio. The present study shows that p73 protein is likely to play important roles in skin differentiation rather than proliferation or carcinogenesis of the skin.</description><subject>Biomarkers, Tumor - analysis</subject><subject>carcinogenesis</subject><subject>Carcinoma, Basal Cell - metabolism</subject><subject>Carcinoma, Basal Cell - pathology</subject><subject>Cell Proliferation</subject><subject>differentiation</subject><subject>DNA-Binding Proteins - biosynthesis</subject><subject>Genes, Tumor Suppressor</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Keratosis, Seborrheic - metabolism</subject><subject>Keratosis, Seborrheic - pathology</subject><subject>Ki-67 Antigen - metabolism</subject><subject>Neoplasms, Squamous Cell - metabolism</subject><subject>Neoplasms, Squamous Cell - pathology</subject><subject>Nuclear Proteins - biosynthesis</subject><subject>p53</subject><subject>p73</subject><subject>skin</subject><subject>Skin - metabolism</subject><subject>Skin Diseases - metabolism</subject><subject>Skin Diseases - pathology</subject><subject>Skin Neoplasms - metabolism</subject><subject>Skin Neoplasms - pathology</subject><subject>Tumor Protein p73</subject><subject>Tumor Suppressor Protein p53 - biosynthesis</subject><subject>Tumor Suppressor Proteins</subject><issn>1320-5463</issn><issn>1440-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqNkEFPwyAYhonRuDn9C6Ynb61QoNCDMTrntrhMEzUeCaWQdOvaCZt2_15ql3mVCx_wPh_wABAgGCE_rhcRIgSGiMcsiiEkEUSMsag5Av3DwbGvcQxDShLcA2fOLaBP4QSegh6iNOUYwT64HTVrq50r6iqoTbBmOCiqoKrtSpaBW_paVnmwtnVZGG3lpvjS3XapW8adgxMjS6cv9vMAvD-O3oaTcPY8ng7vZqGilLJQJpwbxTMZ6yRVisIM58YgxUmMEpLrRKYmhinWOeVU-QXNuPafgDxXyuQED8BV19c_5XOr3UasCqd0WcpK11snUEpQAgn3Qd4Fla2ds9qItS1W0u4EgqKVJxaidSRaR6KVJ37licajl_s7ttlK53_g3pYP3HSB76LUu383Fi_TeVt5Puz4wm10c-ClXYqEYUbFx3wsnl7ZeILuHwTFP5oUjJg</recordid><startdate>200412</startdate><enddate>200412</enddate><creator>Kamiya, Makoto</creator><creator>Takeuchi, Yuko</creator><creator>Katho, Mari</creator><creator>Yokoo, Hideaki</creator><creator>Sasaki, Atsushi</creator><creator>Nakazato, Yoichi</creator><general>Blackwell Science Pty</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>7TO</scope><scope>H94</scope></search><sort><creationdate>200412</creationdate><title>Expression of p73 in normal skin and proliferative skin lesions</title><author>Kamiya, Makoto ; Takeuchi, Yuko ; Katho, Mari ; Yokoo, Hideaki ; Sasaki, Atsushi ; Nakazato, Yoichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5557-a688fc8ba2e69cc50b3dff1c842164de6a9f2093ed585ca9f5b8e82708dccfd43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Biomarkers, Tumor - analysis</topic><topic>carcinogenesis</topic><topic>Carcinoma, Basal Cell - metabolism</topic><topic>Carcinoma, Basal Cell - pathology</topic><topic>Cell Proliferation</topic><topic>differentiation</topic><topic>DNA-Binding Proteins - biosynthesis</topic><topic>Genes, Tumor Suppressor</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Keratosis, Seborrheic - metabolism</topic><topic>Keratosis, Seborrheic - pathology</topic><topic>Ki-67 Antigen - metabolism</topic><topic>Neoplasms, Squamous Cell - metabolism</topic><topic>Neoplasms, Squamous Cell - pathology</topic><topic>Nuclear Proteins - biosynthesis</topic><topic>p53</topic><topic>p73</topic><topic>skin</topic><topic>Skin - metabolism</topic><topic>Skin Diseases - metabolism</topic><topic>Skin Diseases - pathology</topic><topic>Skin Neoplasms - metabolism</topic><topic>Skin Neoplasms - pathology</topic><topic>Tumor Protein p73</topic><topic>Tumor Suppressor Protein p53 - biosynthesis</topic><topic>Tumor Suppressor Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kamiya, Makoto</creatorcontrib><creatorcontrib>Takeuchi, Yuko</creatorcontrib><creatorcontrib>Katho, Mari</creatorcontrib><creatorcontrib>Yokoo, Hideaki</creatorcontrib><creatorcontrib>Sasaki, Atsushi</creatorcontrib><creatorcontrib>Nakazato, Yoichi</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>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Pathology international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kamiya, Makoto</au><au>Takeuchi, Yuko</au><au>Katho, Mari</au><au>Yokoo, Hideaki</au><au>Sasaki, Atsushi</au><au>Nakazato, Yoichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of p73 in normal skin and proliferative skin lesions</atitle><jtitle>Pathology international</jtitle><addtitle>Pathol Int</addtitle><date>2004-12</date><risdate>2004</risdate><volume>54</volume><issue>12</issue><spage>890</spage><epage>895</epage><pages>890-895</pages><issn>1320-5463</issn><eissn>1440-1827</eissn><abstract>The p73 gene is a member of the p53 gene family and the structure and functions of p73 protein are similar to those of  p53.  However,  these  two  proteins  have  different  roles. In the present study, p73 protein was found immunohistochemically to be distributed in the basal cells of the epidermis, columnar basal cells in the hair follicle and peripheral cells without lipid droplets in the sebaceous and meibomian glands; it was expressed strongly in tumor cells in basal cell carcinomas and in the basal cell‐like cells in seborrheic keratosis, and weakly or negatively in the squamous cell‐like cells in seborrheic keratosis and in the tumor cells in squamous cell carcinomas. No relationship was detected between p73 and p53 protein distribution and between p73 protein expression and the proliferative potential, as shown by the Ki‐67 immunopositive cell ratio. The present study shows that p73 protein is likely to play important roles in skin differentiation rather than proliferation or carcinogenesis of the skin.</abstract><cop>Melbourne, Australia</cop><pub>Blackwell Science Pty</pub><pmid>15598310</pmid><doi>10.1111/j.1440-1827.2004.01777.x</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1320-5463
ispartof Pathology international, 2004-12, Vol.54 (12), p.890-895
issn 1320-5463
1440-1827
language eng
recordid cdi_proquest_miscellaneous_19416048
source Wiley
subjects Biomarkers, Tumor - analysis
carcinogenesis
Carcinoma, Basal Cell - metabolism
Carcinoma, Basal Cell - pathology
Cell Proliferation
differentiation
DNA-Binding Proteins - biosynthesis
Genes, Tumor Suppressor
Humans
Immunohistochemistry
Keratosis, Seborrheic - metabolism
Keratosis, Seborrheic - pathology
Ki-67 Antigen - metabolism
Neoplasms, Squamous Cell - metabolism
Neoplasms, Squamous Cell - pathology
Nuclear Proteins - biosynthesis
p53
p73
skin
Skin - metabolism
Skin Diseases - metabolism
Skin Diseases - pathology
Skin Neoplasms - metabolism
Skin Neoplasms - pathology
Tumor Protein p73
Tumor Suppressor Protein p53 - biosynthesis
Tumor Suppressor Proteins
title Expression of p73 in normal skin and proliferative skin lesions
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T16%3A39%3A52IST&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=Expression%20of%20p73%20in%20normal%20skin%20and%20proliferative%20skin%20lesions&rft.jtitle=Pathology%20international&rft.au=Kamiya,%20Makoto&rft.date=2004-12&rft.volume=54&rft.issue=12&rft.spage=890&rft.epage=895&rft.pages=890-895&rft.issn=1320-5463&rft.eissn=1440-1827&rft_id=info:doi/10.1111/j.1440-1827.2004.01777.x&rft_dat=%3Cproquest_cross%3E19416048%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c5557-a688fc8ba2e69cc50b3dff1c842164de6a9f2093ed585ca9f5b8e82708dccfd43%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=19416048&rft_id=info:pmid/15598310&rfr_iscdi=true