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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...
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Published in: | Pathology international 2004-12, Vol.54 (12), p.890-895 |
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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 |
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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> |
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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 |
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