Clinical relevance and accuracy of p63 and TTF-1 for better approach of small cell lung carcinoma versus poorly differentiated nonkeratinizing squamous cell carcinoma
Lung cancer high mortality rate remains a major problem, despite the actual progress in its early detection and therapeutic design. Since lung cancer' treatment requires separation of tumors in small cell carcinoma and non-small cell carcinoma, the histopathological diagnosis focuses on this ba...
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Veröffentlicht in: | Romanian journal of morphology and embryology 2019, Vol.60 (1), p.139-143 |
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creator | Gurguş, Daniela Grigoraş, Mirela Loredana Motoc, Andrei Gheorghe Marius Zamfir, Carmen Lăcrămioara Cornianu, Mărioara Faur, Cosmin Ioan Pop, Daniel Laurenţiu Folescu, Roxana |
description | Lung cancer high mortality rate remains a major problem, despite the actual progress in its early detection and therapeutic design. Since lung cancer' treatment requires separation of tumors in small cell carcinoma and non-small cell carcinoma, the histopathological diagnosis focuses on this basic distinction, while immunohistochemistry contributes considerably to confirm the diagnosis accuracy. In order to check the assumption that p63 is a useful marker for squamous cellular differentiation, we used two antibodies: anti-p63 and anti-thyroid transcription factor-1 (TTF-1), based on their immunoexpression to differentiate small cell lung carcinoma (SCLC) from poorly differentiated nonkeratinizing squamous cell carcinoma (SCC). Our study included 48 cases of lung carcinoma (lung biopsies and wedge resection formalin-fixed and paraffin-embedded). The 48 cases included 23 SCLCs and 25 poorly differentiated nonkeratinizing SCC. The expressions of p63 and TTF-1, respectively, proved to be useful in distinguishing SCLC from poorly differentiated nonkeratinizing SCC, on surgical and biopsic sections. The p63 positivity and TTF-1 negative expression consequently indicated a poorly differentiated nonkeratinizing SCC, while the opposite immunostaining pattern was flagged in SCLC. Our results are useful for a targeted therapy, as long as they point out a significant role in marking of the correct diagnosis of lung tumors. |
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Since lung cancer' treatment requires separation of tumors in small cell carcinoma and non-small cell carcinoma, the histopathological diagnosis focuses on this basic distinction, while immunohistochemistry contributes considerably to confirm the diagnosis accuracy. In order to check the assumption that p63 is a useful marker for squamous cellular differentiation, we used two antibodies: anti-p63 and anti-thyroid transcription factor-1 (TTF-1), based on their immunoexpression to differentiate small cell lung carcinoma (SCLC) from poorly differentiated nonkeratinizing squamous cell carcinoma (SCC). Our study included 48 cases of lung carcinoma (lung biopsies and wedge resection formalin-fixed and paraffin-embedded). The 48 cases included 23 SCLCs and 25 poorly differentiated nonkeratinizing SCC. The expressions of p63 and TTF-1, respectively, proved to be useful in distinguishing SCLC from poorly differentiated nonkeratinizing SCC, on surgical and biopsic sections. The p63 positivity and TTF-1 negative expression consequently indicated a poorly differentiated nonkeratinizing SCC, while the opposite immunostaining pattern was flagged in SCLC. 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Since lung cancer' treatment requires separation of tumors in small cell carcinoma and non-small cell carcinoma, the histopathological diagnosis focuses on this basic distinction, while immunohistochemistry contributes considerably to confirm the diagnosis accuracy. In order to check the assumption that p63 is a useful marker for squamous cellular differentiation, we used two antibodies: anti-p63 and anti-thyroid transcription factor-1 (TTF-1), based on their immunoexpression to differentiate small cell lung carcinoma (SCLC) from poorly differentiated nonkeratinizing squamous cell carcinoma (SCC). Our study included 48 cases of lung carcinoma (lung biopsies and wedge resection formalin-fixed and paraffin-embedded). The 48 cases included 23 SCLCs and 25 poorly differentiated nonkeratinizing SCC. The expressions of p63 and TTF-1, respectively, proved to be useful in distinguishing SCLC from poorly differentiated nonkeratinizing SCC, on surgical and biopsic sections. The p63 positivity and TTF-1 negative expression consequently indicated a poorly differentiated nonkeratinizing SCC, while the opposite immunostaining pattern was flagged in SCLC. Our results are useful for a targeted therapy, as long as they point out a significant role in marking of the correct diagnosis of lung tumors.</description><subject>Biomarkers, Tumor - metabolism</subject><subject>Carcinoma, Squamous Cell - metabolism</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Cell Differentiation - physiology</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Female</subject><subject>Humans</subject><subject>Lung Neoplasms - metabolism</subject><subject>Lung Neoplasms - pathology</subject><subject>Male</subject><subject>Membrane Proteins - metabolism</subject><subject>Small Cell Lung Carcinoma - metabolism</subject><subject>Small Cell Lung Carcinoma - pathology</subject><subject>Transcription Factors - metabolism</subject><issn>1220-0522</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE1PwzAMhnsAsWnsL6AcuVTKRz-SI5oYICFxGefKS1wIpEmXtJPGD-J30o2BD7ZkP3712hfZnHFOc1pyPsuWKX3QKSpaUlFfZTPBeCWkkPPse-WstxociehwD14jAW8IaD1G0AcSWtJX4tTbbNY5I22IZIvDgJFA38cA-v0IpQ6cIxqn5Eb_RjREbX3ogOwxpjGRPoToDsTYtsWIfrAwoCE--E-MMEwmvuy0lnYjdGHCT0r_ItfZZQsu4fJcF9nr-n6zesyfXx6eVnfPec8ZG_ICpClLzbTipq2kFCUWQskaFNcalKk4aCpB1oxJqgpWy1Ypo-V2mpoCuFhkt7-602G7EdPQdDYdrYDHyVXDeckYrQp1RG_O6Ljt0DR9tB3EQ_P3W_ED6QF4Uw</recordid><startdate>2019</startdate><enddate>2019</enddate><creator>Gurguş, Daniela</creator><creator>Grigoraş, Mirela Loredana</creator><creator>Motoc, Andrei Gheorghe Marius</creator><creator>Zamfir, Carmen Lăcrămioara</creator><creator>Cornianu, Mărioara</creator><creator>Faur, Cosmin Ioan</creator><creator>Pop, Daniel Laurenţiu</creator><creator>Folescu, Roxana</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>2019</creationdate><title>Clinical relevance and accuracy of p63 and TTF-1 for better approach of small cell lung carcinoma versus poorly differentiated nonkeratinizing squamous cell carcinoma</title><author>Gurguş, Daniela ; Grigoraş, Mirela Loredana ; Motoc, Andrei Gheorghe Marius ; Zamfir, Carmen Lăcrămioara ; Cornianu, Mărioara ; Faur, Cosmin Ioan ; Pop, Daniel Laurenţiu ; Folescu, Roxana</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p211t-4a8d55c1c92df68835e43987a92cca9d62ac08a87118094178f99dc8bccad4a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Biomarkers, Tumor - metabolism</topic><topic>Carcinoma, Squamous Cell - metabolism</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Cell Differentiation - physiology</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Female</topic><topic>Humans</topic><topic>Lung Neoplasms - metabolism</topic><topic>Lung Neoplasms - pathology</topic><topic>Male</topic><topic>Membrane Proteins - metabolism</topic><topic>Small Cell Lung Carcinoma - metabolism</topic><topic>Small Cell Lung Carcinoma - pathology</topic><topic>Transcription Factors - metabolism</topic><toplevel>online_resources</toplevel><creatorcontrib>Gurguş, Daniela</creatorcontrib><creatorcontrib>Grigoraş, Mirela Loredana</creatorcontrib><creatorcontrib>Motoc, Andrei Gheorghe Marius</creatorcontrib><creatorcontrib>Zamfir, Carmen Lăcrămioara</creatorcontrib><creatorcontrib>Cornianu, Mărioara</creatorcontrib><creatorcontrib>Faur, Cosmin Ioan</creatorcontrib><creatorcontrib>Pop, Daniel Laurenţiu</creatorcontrib><creatorcontrib>Folescu, Roxana</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Romanian journal of morphology and embryology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gurguş, Daniela</au><au>Grigoraş, Mirela Loredana</au><au>Motoc, Andrei Gheorghe Marius</au><au>Zamfir, Carmen Lăcrămioara</au><au>Cornianu, Mărioara</au><au>Faur, Cosmin Ioan</au><au>Pop, Daniel Laurenţiu</au><au>Folescu, Roxana</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical relevance and accuracy of p63 and TTF-1 for better approach of small cell lung carcinoma versus poorly differentiated nonkeratinizing squamous cell carcinoma</atitle><jtitle>Romanian journal of morphology and embryology</jtitle><addtitle>Rom J Morphol Embryol</addtitle><date>2019</date><risdate>2019</risdate><volume>60</volume><issue>1</issue><spage>139</spage><epage>143</epage><pages>139-143</pages><issn>1220-0522</issn><abstract>Lung cancer high mortality rate remains a major problem, despite the actual progress in its early detection and therapeutic design. Since lung cancer' treatment requires separation of tumors in small cell carcinoma and non-small cell carcinoma, the histopathological diagnosis focuses on this basic distinction, while immunohistochemistry contributes considerably to confirm the diagnosis accuracy. In order to check the assumption that p63 is a useful marker for squamous cellular differentiation, we used two antibodies: anti-p63 and anti-thyroid transcription factor-1 (TTF-1), based on their immunoexpression to differentiate small cell lung carcinoma (SCLC) from poorly differentiated nonkeratinizing squamous cell carcinoma (SCC). Our study included 48 cases of lung carcinoma (lung biopsies and wedge resection formalin-fixed and paraffin-embedded). The 48 cases included 23 SCLCs and 25 poorly differentiated nonkeratinizing SCC. The expressions of p63 and TTF-1, respectively, proved to be useful in distinguishing SCLC from poorly differentiated nonkeratinizing SCC, on surgical and biopsic sections. The p63 positivity and TTF-1 negative expression consequently indicated a poorly differentiated nonkeratinizing SCC, while the opposite immunostaining pattern was flagged in SCLC. Our results are useful for a targeted therapy, as long as they point out a significant role in marking of the correct diagnosis of lung tumors.</abstract><cop>Romania</cop><pmid>31263838</pmid><tpages>5</tpages></addata></record> |
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subjects | Biomarkers, Tumor - metabolism Carcinoma, Squamous Cell - metabolism Carcinoma, Squamous Cell - pathology Cell Differentiation - physiology DNA-Binding Proteins - metabolism Female Humans Lung Neoplasms - metabolism Lung Neoplasms - pathology Male Membrane Proteins - metabolism Small Cell Lung Carcinoma - metabolism Small Cell Lung Carcinoma - pathology Transcription Factors - metabolism |
title | Clinical relevance and accuracy of p63 and TTF-1 for better approach of small cell lung carcinoma versus poorly differentiated nonkeratinizing squamous cell carcinoma |
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