Role of Bcl-2, p53, and Ki-67 expression in basal cell carcinoma and their association with aggressive and non-aggressive histological phenotypes
Introduction There is increasing evidence that immunohistochemical expression of p53, Ki-67, and Bcl-2 is associated with aggressive (aBCC) and less aggressive (nBCC) histological subtypes and may have a prognostic role. Aim: To investigate the clinicopathological features and immunohistochemical ex...
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Veröffentlicht in: | Postȩpy dermatologii i alergologii 2022-06, Vol.39 (3), p.517-523 |
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creator | Mendez-Flores, Raúl Martínez-Fernández, Diana Vega-De la Torre, Diego Zambrano-Román, Marianela Muñoz-Valle, José Toledo-Lelevier, Mario Guevara-Gutiérrez, Elizabeth Ramírez-Padilla, Marisol Valdés-Alvarado, Emmanuel |
description | Introduction There is increasing evidence that immunohistochemical expression of p53, Ki-67, and Bcl-2 is associated with aggressive (aBCC) and less aggressive (nBCC) histological subtypes and may have a prognostic role. Aim: To investigate the clinicopathological features and immunohistochemical expressions of p53, Ki-67, and Bcl-2 in cutaneous basal cell carcinoma focusing on histological subtypes. Their roles and possible interactions in the development and progression of BCC are discussed. Material and methods A total of 50 BCC samples from 50 patients from Western Mexico between June 2018 and June 2019 were included. Paraffin-embedded samples were immunostained with p53, Ki-67, and Bcl-2 antibodies. Semi-quantitative analysis was performed to determine the intensity and positivity of immunostained cells. Parametrical and non-parametrical tests were performed according to the sample’s distribution. Results Samples included 21 nBCC and 29 aBCC. The statistical analysis showed statistical association when grouped as non-aggressive and aggressive subtypes for p53 (p = 0.04) and Bcl-2 (p < 0.01). An inverse negative correlation was found between age and Bcl-2 expression. No statistical association was found between Ki-67 immunoreactivity and any of the other variables. Conclusions We found that a high expression of Bcl-2 and a low expression of p53 was associated with more indolent histopathological features of BCC and therefore better outcomes. These findings suggest that examination of p53 and Bcl-2 expression in BCC patients may provide valuable prognostic information. These biomarkers may play a role in the development and progression of some cases of BCC. |
doi_str_mv | 10.5114/ada.2022.117598 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9326923</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2701036783</sourcerecordid><originalsourceid>FETCH-LOGICAL-c328t-76f7af25e5ff0a6630c05ae602695061ea6a50e1d436b4dccd3e7200b5ee07833</originalsourceid><addsrcrecordid>eNpdkU1r3DAQhkVoaZY0514FufQQb_RhSetLoQ1pEhIolBZ6E7PyeK3glVzJm4-f0X8cex1K2jloQHrm1cy8hHzgbKk4L8-ghqVgQiw5N6paHZCFEFVVMFbqN2TBdSkKWalfh-Q45zs2huZSr6p35FCqSjEu-IL8-R47pLGhX1xXiFPaK3lKIdT0xhfaUHzsE-bsY6A-0DVk6KjDbjwgOR_iFvbw0KJPFHKOzsMw0Q9-aClsNvvqe9xTIYbi1VXr8xC7uPFuFO1bDHF46jG_J28b6DIev-Qj8vPrxY_zq-L22-X1-efbwkmxGgqjGwONUKiahoHWkjmmADUTepxNcwQNiiGvS6nXZe1cLdEIxtYKkZmVlEfk06zb79ZbrB2GIUFn--S3kJ5sBG__fQm-tZt4bys5fiEmgY8vAin-3mEe7NbnaTkQMO6yFYZxZkqjJ_TkP_Qu7lIYx5spqeeOzmbKpZhzwuZvM5zZyXE7Om4nx-3suHwGmwaeXg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2701036783</pqid></control><display><type>article</type><title>Role of Bcl-2, p53, and Ki-67 expression in basal cell carcinoma and their association with aggressive and non-aggressive histological phenotypes</title><source>PubMed Central Open Access</source><source>PubMed Central</source><creator>Mendez-Flores, Raúl ; Martínez-Fernández, Diana ; Vega-De la Torre, Diego ; Zambrano-Román, Marianela ; Muñoz-Valle, José ; Toledo-Lelevier, Mario ; Guevara-Gutiérrez, Elizabeth ; Ramírez-Padilla, Marisol ; Valdés-Alvarado, Emmanuel</creator><creatorcontrib>Mendez-Flores, Raúl ; Martínez-Fernández, Diana ; Vega-De la Torre, Diego ; Zambrano-Román, Marianela ; Muñoz-Valle, José ; Toledo-Lelevier, Mario ; Guevara-Gutiérrez, Elizabeth ; Ramírez-Padilla, Marisol ; Valdés-Alvarado, Emmanuel</creatorcontrib><description>Introduction There is increasing evidence that immunohistochemical expression of p53, Ki-67, and Bcl-2 is associated with aggressive (aBCC) and less aggressive (nBCC) histological subtypes and may have a prognostic role. Aim: To investigate the clinicopathological features and immunohistochemical expressions of p53, Ki-67, and Bcl-2 in cutaneous basal cell carcinoma focusing on histological subtypes. Their roles and possible interactions in the development and progression of BCC are discussed. Material and methods A total of 50 BCC samples from 50 patients from Western Mexico between June 2018 and June 2019 were included. Paraffin-embedded samples were immunostained with p53, Ki-67, and Bcl-2 antibodies. Semi-quantitative analysis was performed to determine the intensity and positivity of immunostained cells. Parametrical and non-parametrical tests were performed according to the sample’s distribution. Results Samples included 21 nBCC and 29 aBCC. The statistical analysis showed statistical association when grouped as non-aggressive and aggressive subtypes for p53 (p = 0.04) and Bcl-2 (p < 0.01). An inverse negative correlation was found between age and Bcl-2 expression. No statistical association was found between Ki-67 immunoreactivity and any of the other variables. Conclusions We found that a high expression of Bcl-2 and a low expression of p53 was associated with more indolent histopathological features of BCC and therefore better outcomes. These findings suggest that examination of p53 and Bcl-2 expression in BCC patients may provide valuable prognostic information. These biomarkers may play a role in the development and progression of some cases of BCC.</description><identifier>ISSN: 1642-395X</identifier><identifier>EISSN: 2299-0046</identifier><identifier>DOI: 10.5114/ada.2022.117598</identifier><identifier>PMID: 35950121</identifier><language>eng</language><publisher>Poznan: Termedia Publishing House</publisher><subject>Antibodies ; Biomarkers ; Cancer ; Cell growth ; Dermatology ; Ethics ; Medical prognosis ; Original Paper ; Proteins ; Skin cancer ; Statistical analysis ; Tumors</subject><ispartof>Postȩpy dermatologii i alergologii, 2022-06, Vol.39 (3), p.517-523</ispartof><rights>2022. This work is published under http://creativecommons.org/licenses/by-nc-sa/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright: © 2022 Termedia Sp. z o. o. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c328t-76f7af25e5ff0a6630c05ae602695061ea6a50e1d436b4dccd3e7200b5ee07833</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/PMC9326923/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9326923/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids></links><search><creatorcontrib>Mendez-Flores, Raúl</creatorcontrib><creatorcontrib>Martínez-Fernández, Diana</creatorcontrib><creatorcontrib>Vega-De la Torre, Diego</creatorcontrib><creatorcontrib>Zambrano-Román, Marianela</creatorcontrib><creatorcontrib>Muñoz-Valle, José</creatorcontrib><creatorcontrib>Toledo-Lelevier, Mario</creatorcontrib><creatorcontrib>Guevara-Gutiérrez, Elizabeth</creatorcontrib><creatorcontrib>Ramírez-Padilla, Marisol</creatorcontrib><creatorcontrib>Valdés-Alvarado, Emmanuel</creatorcontrib><title>Role of Bcl-2, p53, and Ki-67 expression in basal cell carcinoma and their association with aggressive and non-aggressive histological phenotypes</title><title>Postȩpy dermatologii i alergologii</title><description>Introduction There is increasing evidence that immunohistochemical expression of p53, Ki-67, and Bcl-2 is associated with aggressive (aBCC) and less aggressive (nBCC) histological subtypes and may have a prognostic role. Aim: To investigate the clinicopathological features and immunohistochemical expressions of p53, Ki-67, and Bcl-2 in cutaneous basal cell carcinoma focusing on histological subtypes. Their roles and possible interactions in the development and progression of BCC are discussed. Material and methods A total of 50 BCC samples from 50 patients from Western Mexico between June 2018 and June 2019 were included. Paraffin-embedded samples were immunostained with p53, Ki-67, and Bcl-2 antibodies. Semi-quantitative analysis was performed to determine the intensity and positivity of immunostained cells. Parametrical and non-parametrical tests were performed according to the sample’s distribution. Results Samples included 21 nBCC and 29 aBCC. The statistical analysis showed statistical association when grouped as non-aggressive and aggressive subtypes for p53 (p = 0.04) and Bcl-2 (p < 0.01). An inverse negative correlation was found between age and Bcl-2 expression. No statistical association was found between Ki-67 immunoreactivity and any of the other variables. Conclusions We found that a high expression of Bcl-2 and a low expression of p53 was associated with more indolent histopathological features of BCC and therefore better outcomes. These findings suggest that examination of p53 and Bcl-2 expression in BCC patients may provide valuable prognostic information. These biomarkers may play a role in the development and progression of some cases of BCC.</description><subject>Antibodies</subject><subject>Biomarkers</subject><subject>Cancer</subject><subject>Cell growth</subject><subject>Dermatology</subject><subject>Ethics</subject><subject>Medical prognosis</subject><subject>Original Paper</subject><subject>Proteins</subject><subject>Skin cancer</subject><subject>Statistical analysis</subject><subject>Tumors</subject><issn>1642-395X</issn><issn>2299-0046</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpdkU1r3DAQhkVoaZY0514FufQQb_RhSetLoQ1pEhIolBZ6E7PyeK3glVzJm4-f0X8cex1K2jloQHrm1cy8hHzgbKk4L8-ghqVgQiw5N6paHZCFEFVVMFbqN2TBdSkKWalfh-Q45zs2huZSr6p35FCqSjEu-IL8-R47pLGhX1xXiFPaK3lKIdT0xhfaUHzsE-bsY6A-0DVk6KjDbjwgOR_iFvbw0KJPFHKOzsMw0Q9-aClsNvvqe9xTIYbi1VXr8xC7uPFuFO1bDHF46jG_J28b6DIev-Qj8vPrxY_zq-L22-X1-efbwkmxGgqjGwONUKiahoHWkjmmADUTepxNcwQNiiGvS6nXZe1cLdEIxtYKkZmVlEfk06zb79ZbrB2GIUFn--S3kJ5sBG__fQm-tZt4bys5fiEmgY8vAin-3mEe7NbnaTkQMO6yFYZxZkqjJ_TkP_Qu7lIYx5spqeeOzmbKpZhzwuZvM5zZyXE7Om4nx-3suHwGmwaeXg</recordid><startdate>20220601</startdate><enddate>20220601</enddate><creator>Mendez-Flores, Raúl</creator><creator>Martínez-Fernández, Diana</creator><creator>Vega-De la Torre, Diego</creator><creator>Zambrano-Román, Marianela</creator><creator>Muñoz-Valle, José</creator><creator>Toledo-Lelevier, Mario</creator><creator>Guevara-Gutiérrez, Elizabeth</creator><creator>Ramírez-Padilla, Marisol</creator><creator>Valdés-Alvarado, Emmanuel</creator><general>Termedia Publishing House</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BYOGL</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20220601</creationdate><title>Role of Bcl-2, p53, and Ki-67 expression in basal cell carcinoma and their association with aggressive and non-aggressive histological phenotypes</title><author>Mendez-Flores, Raúl ; Martínez-Fernández, Diana ; Vega-De la Torre, Diego ; Zambrano-Román, Marianela ; Muñoz-Valle, José ; Toledo-Lelevier, Mario ; Guevara-Gutiérrez, Elizabeth ; Ramírez-Padilla, Marisol ; Valdés-Alvarado, Emmanuel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c328t-76f7af25e5ff0a6630c05ae602695061ea6a50e1d436b4dccd3e7200b5ee07833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antibodies</topic><topic>Biomarkers</topic><topic>Cancer</topic><topic>Cell growth</topic><topic>Dermatology</topic><topic>Ethics</topic><topic>Medical prognosis</topic><topic>Original Paper</topic><topic>Proteins</topic><topic>Skin cancer</topic><topic>Statistical analysis</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mendez-Flores, Raúl</creatorcontrib><creatorcontrib>Martínez-Fernández, Diana</creatorcontrib><creatorcontrib>Vega-De la Torre, Diego</creatorcontrib><creatorcontrib>Zambrano-Román, Marianela</creatorcontrib><creatorcontrib>Muñoz-Valle, José</creatorcontrib><creatorcontrib>Toledo-Lelevier, Mario</creatorcontrib><creatorcontrib>Guevara-Gutiérrez, Elizabeth</creatorcontrib><creatorcontrib>Ramírez-Padilla, Marisol</creatorcontrib><creatorcontrib>Valdés-Alvarado, Emmanuel</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>East Europe, Central Europe Database</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 Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Access via ProQuest (Open Access)</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Postȩpy dermatologii i alergologii</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mendez-Flores, Raúl</au><au>Martínez-Fernández, Diana</au><au>Vega-De la Torre, Diego</au><au>Zambrano-Román, Marianela</au><au>Muñoz-Valle, José</au><au>Toledo-Lelevier, Mario</au><au>Guevara-Gutiérrez, Elizabeth</au><au>Ramírez-Padilla, Marisol</au><au>Valdés-Alvarado, Emmanuel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of Bcl-2, p53, and Ki-67 expression in basal cell carcinoma and their association with aggressive and non-aggressive histological phenotypes</atitle><jtitle>Postȩpy dermatologii i alergologii</jtitle><date>2022-06-01</date><risdate>2022</risdate><volume>39</volume><issue>3</issue><spage>517</spage><epage>523</epage><pages>517-523</pages><issn>1642-395X</issn><eissn>2299-0046</eissn><abstract>Introduction There is increasing evidence that immunohistochemical expression of p53, Ki-67, and Bcl-2 is associated with aggressive (aBCC) and less aggressive (nBCC) histological subtypes and may have a prognostic role. Aim: To investigate the clinicopathological features and immunohistochemical expressions of p53, Ki-67, and Bcl-2 in cutaneous basal cell carcinoma focusing on histological subtypes. Their roles and possible interactions in the development and progression of BCC are discussed. Material and methods A total of 50 BCC samples from 50 patients from Western Mexico between June 2018 and June 2019 were included. Paraffin-embedded samples were immunostained with p53, Ki-67, and Bcl-2 antibodies. Semi-quantitative analysis was performed to determine the intensity and positivity of immunostained cells. Parametrical and non-parametrical tests were performed according to the sample’s distribution. Results Samples included 21 nBCC and 29 aBCC. The statistical analysis showed statistical association when grouped as non-aggressive and aggressive subtypes for p53 (p = 0.04) and Bcl-2 (p < 0.01). An inverse negative correlation was found between age and Bcl-2 expression. No statistical association was found between Ki-67 immunoreactivity and any of the other variables. Conclusions We found that a high expression of Bcl-2 and a low expression of p53 was associated with more indolent histopathological features of BCC and therefore better outcomes. These findings suggest that examination of p53 and Bcl-2 expression in BCC patients may provide valuable prognostic information. These biomarkers may play a role in the development and progression of some cases of BCC.</abstract><cop>Poznan</cop><pub>Termedia Publishing House</pub><pmid>35950121</pmid><doi>10.5114/ada.2022.117598</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies Biomarkers Cancer Cell growth Dermatology Ethics Medical prognosis Original Paper Proteins Skin cancer Statistical analysis Tumors |
title | Role of Bcl-2, p53, and Ki-67 expression in basal cell carcinoma and their association with aggressive and non-aggressive histological phenotypes |
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