Quantitative p21(waf-1)/p53 immunohistochemical analysis defines groups of primary invasive breast carcinomas with different prognostic indicators
We used image cytometry to quantify the immunohistochemical expression of p21(waf-1) and p53 in primary breast carcinoma. Ratio analysis of the quantified p53/p21(waf-1) protein expression allowed us to define 3 groups of carcinomas, each characterized by specific pathological and biological profile...
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Veröffentlicht in: | International journal of cancer 2001-03, Vol.95 (2), p.128-134 |
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description | We used image cytometry to quantify the immunohistochemical expression of p21(waf-1) and p53 in primary breast carcinoma. Ratio analysis of the quantified p53/p21(waf-1) protein expression allowed us to define 3 groups of carcinomas, each characterized by specific pathological and biological profiles. The negative (NEG) group, characterized by negligible expression of both proteins, comprised small-sized, low-grade tumors associated with high contents of hormonal receptors and low growth fraction. In the NEG group, Ki-67 labelling index area (%LIa) was the only significant prognostic indicator. The P53H group, characterized by prevalence of p53 %LIa, was constituted by large-sized, high-grade tumors showing low hormonal receptor contents and high growth fraction. In the P53H group, both p53 and Ki-67 were inversely associated with both estrogen receptor (ER) and progesterone receptor (PGR), suggesting that extensive p53 immunostaining is related to poor differentiation and high proliferation. Only N status was prognostically significant in the P53H group. The P21H group, characterized by prevalence of p21(waf-1) %LIa, displayed intermediate pathological and biological features. A significant association between p53 and p21(waf-1) expression suggested functional stabilization of wtp53 and therefore possible DNA damage-dependent G1/S arrest (genetic instability) in the P21H group; P21(waf-1)expression was significantly associated with the presence of node metastasis. Patients in the P21H group had a higher recurrence rate and a shorter disease-free time interval from surgery with respect to the NEG group. Proportional hazard regression analysis disclosed Ki-67 %LIa and, to a lesser degree, PGR %LIa as significant relapse-free survival prognostic indicators. |
doi_str_mv | 10.1002/1097-0215(20010320)95:2<128::AID-IJC1022>3.0.CO;2-D |
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Ratio analysis of the quantified p53/p21(waf-1) protein expression allowed us to define 3 groups of carcinomas, each characterized by specific pathological and biological profiles. The negative (NEG) group, characterized by negligible expression of both proteins, comprised small-sized, low-grade tumors associated with high contents of hormonal receptors and low growth fraction. In the NEG group, Ki-67 labelling index area (%LIa) was the only significant prognostic indicator. The P53H group, characterized by prevalence of p53 %LIa, was constituted by large-sized, high-grade tumors showing low hormonal receptor contents and high growth fraction. In the P53H group, both p53 and Ki-67 were inversely associated with both estrogen receptor (ER) and progesterone receptor (PGR), suggesting that extensive p53 immunostaining is related to poor differentiation and high proliferation. Only N status was prognostically significant in the P53H group. The P21H group, characterized by prevalence of p21(waf-1) %LIa, displayed intermediate pathological and biological features. A significant association between p53 and p21(waf-1) expression suggested functional stabilization of wtp53 and therefore possible DNA damage-dependent G1/S arrest (genetic instability) in the P21H group; P21(waf-1)expression was significantly associated with the presence of node metastasis. Patients in the P21H group had a higher recurrence rate and a shorter disease-free time interval from surgery with respect to the NEG group. Proportional hazard regression analysis disclosed Ki-67 %LIa and, to a lesser degree, PGR %LIa as significant relapse-free survival prognostic indicators.</description><identifier>ISSN: 0020-7136</identifier><identifier>DOI: 10.1002/1097-0215(20010320)95:2<128::AID-IJC1022>3.0.CO;2-D</identifier><identifier>PMID: 11241324</identifier><language>eng</language><publisher>United States</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Breast Neoplasms - diagnosis ; Breast Neoplasms - metabolism ; Carcinoma, Ductal, Breast - diagnosis ; Carcinoma, Ductal, Breast - metabolism ; Carcinoma, Medullary - diagnosis ; Carcinoma, Medullary - metabolism ; Cyclin-Dependent Kinase Inhibitor p21 ; Cyclins - biosynthesis ; Disease-Free Survival ; DNA Damage ; Female ; Humans ; Image Cytometry ; Immunohistochemistry ; Ki-67 Antigen - biosynthesis ; Lymphatic Metastasis ; Middle Aged ; Multivariate Analysis ; Mutation ; Prognosis ; Proportional Hazards Models ; Receptors, Estrogen - biosynthesis ; Receptors, Progesterone - biosynthesis ; Time Factors ; Tumor Suppressor Protein p53 - biosynthesis</subject><ispartof>International journal of cancer, 2001-03, Vol.95 (2), p.128-134</ispartof><rights>Copyright 2001 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11241324$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ceccarelli, C</creatorcontrib><creatorcontrib>Santini, D</creatorcontrib><creatorcontrib>Chieco, P</creatorcontrib><creatorcontrib>Lanciotti, C</creatorcontrib><creatorcontrib>Taffurelli, M</creatorcontrib><creatorcontrib>Paladini, G</creatorcontrib><creatorcontrib>Marrano, D</creatorcontrib><title>Quantitative p21(waf-1)/p53 immunohistochemical analysis defines groups of primary invasive breast carcinomas with different prognostic indicators</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>We used image cytometry to quantify the immunohistochemical expression of p21(waf-1) and p53 in primary breast carcinoma. Ratio analysis of the quantified p53/p21(waf-1) protein expression allowed us to define 3 groups of carcinomas, each characterized by specific pathological and biological profiles. The negative (NEG) group, characterized by negligible expression of both proteins, comprised small-sized, low-grade tumors associated with high contents of hormonal receptors and low growth fraction. In the NEG group, Ki-67 labelling index area (%LIa) was the only significant prognostic indicator. The P53H group, characterized by prevalence of p53 %LIa, was constituted by large-sized, high-grade tumors showing low hormonal receptor contents and high growth fraction. In the P53H group, both p53 and Ki-67 were inversely associated with both estrogen receptor (ER) and progesterone receptor (PGR), suggesting that extensive p53 immunostaining is related to poor differentiation and high proliferation. Only N status was prognostically significant in the P53H group. The P21H group, characterized by prevalence of p21(waf-1) %LIa, displayed intermediate pathological and biological features. A significant association between p53 and p21(waf-1) expression suggested functional stabilization of wtp53 and therefore possible DNA damage-dependent G1/S arrest (genetic instability) in the P21H group; P21(waf-1)expression was significantly associated with the presence of node metastasis. Patients in the P21H group had a higher recurrence rate and a shorter disease-free time interval from surgery with respect to the NEG group. Proportional hazard regression analysis disclosed Ki-67 %LIa and, to a lesser degree, PGR %LIa as significant relapse-free survival prognostic indicators.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Breast Neoplasms - diagnosis</subject><subject>Breast Neoplasms - metabolism</subject><subject>Carcinoma, Ductal, Breast - diagnosis</subject><subject>Carcinoma, Ductal, Breast - metabolism</subject><subject>Carcinoma, Medullary - diagnosis</subject><subject>Carcinoma, Medullary - metabolism</subject><subject>Cyclin-Dependent Kinase Inhibitor p21</subject><subject>Cyclins - biosynthesis</subject><subject>Disease-Free Survival</subject><subject>DNA Damage</subject><subject>Female</subject><subject>Humans</subject><subject>Image Cytometry</subject><subject>Immunohistochemistry</subject><subject>Ki-67 Antigen - biosynthesis</subject><subject>Lymphatic Metastasis</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Mutation</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Receptors, Estrogen - biosynthesis</subject><subject>Receptors, Progesterone - biosynthesis</subject><subject>Time Factors</subject><subject>Tumor Suppressor Protein p53 - biosynthesis</subject><issn>0020-7136</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kMtKBDEQRbNQfP-CZCW66LHy6EdGEWR8jQgi6HrIJNVOpDtpO2nF3_CLbXFc1aLuOVRdQs4YTBgAP2Wgygw4y485AAPB4UTlU37OeDWdXs6vsvn9jAHnF2ICk9njGc-uNsjOSEJWMlFsk90Y30aS5SC3yDZjXDLB5Q75fhq0Ty7p5D6Qdpwdf-o6YyenXS6oa9vBh5WLKZgVts7ohmqvm6_oIrVYO4-RvvZh6CINNe161-r-izr_oeOvbtmjjoka3RvnQ6sj_XRpRa2ra-zRp5EIrz7E5MwI2dGfQh_3yWatm4gH67lHXm6un2d32cPj7Xx2-ZB1HMqUWa6tFAhao1navJJYF5VhlVJFbnJjUBnMKyyVQqFQmpqLwjI5buWytLISe-Tozzte8T5gTIvWRYNNoz2GIS5KKEpQUIzBw3VwWLZoF-s_F_8tih-LZn37</recordid><startdate>20010320</startdate><enddate>20010320</enddate><creator>Ceccarelli, C</creator><creator>Santini, D</creator><creator>Chieco, P</creator><creator>Lanciotti, C</creator><creator>Taffurelli, M</creator><creator>Paladini, G</creator><creator>Marrano, D</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>20010320</creationdate><title>Quantitative p21(waf-1)/p53 immunohistochemical analysis defines groups of primary invasive breast carcinomas with different prognostic indicators</title><author>Ceccarelli, C ; Santini, D ; Chieco, P ; Lanciotti, C ; Taffurelli, M ; Paladini, G ; Marrano, D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p207t-d2ad43e0aaecbd584ef68c189965c5cce9ce58e799e39e4cf236d149654b7d483</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>Breast Neoplasms - diagnosis</topic><topic>Breast Neoplasms - metabolism</topic><topic>Carcinoma, Ductal, Breast - diagnosis</topic><topic>Carcinoma, Ductal, Breast - metabolism</topic><topic>Carcinoma, Medullary - diagnosis</topic><topic>Carcinoma, Medullary - metabolism</topic><topic>Cyclin-Dependent Kinase Inhibitor p21</topic><topic>Cyclins - biosynthesis</topic><topic>Disease-Free Survival</topic><topic>DNA Damage</topic><topic>Female</topic><topic>Humans</topic><topic>Image Cytometry</topic><topic>Immunohistochemistry</topic><topic>Ki-67 Antigen - biosynthesis</topic><topic>Lymphatic Metastasis</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Mutation</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Receptors, Estrogen - biosynthesis</topic><topic>Receptors, Progesterone - biosynthesis</topic><topic>Time Factors</topic><topic>Tumor Suppressor Protein p53 - biosynthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ceccarelli, C</creatorcontrib><creatorcontrib>Santini, D</creatorcontrib><creatorcontrib>Chieco, P</creatorcontrib><creatorcontrib>Lanciotti, C</creatorcontrib><creatorcontrib>Taffurelli, M</creatorcontrib><creatorcontrib>Paladini, G</creatorcontrib><creatorcontrib>Marrano, D</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>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ceccarelli, C</au><au>Santini, D</au><au>Chieco, P</au><au>Lanciotti, C</au><au>Taffurelli, M</au><au>Paladini, G</au><au>Marrano, D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative p21(waf-1)/p53 immunohistochemical analysis defines groups of primary invasive breast carcinomas with different prognostic indicators</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2001-03-20</date><risdate>2001</risdate><volume>95</volume><issue>2</issue><spage>128</spage><epage>134</epage><pages>128-134</pages><issn>0020-7136</issn><abstract>We used image cytometry to quantify the immunohistochemical expression of p21(waf-1) and p53 in primary breast carcinoma. Ratio analysis of the quantified p53/p21(waf-1) protein expression allowed us to define 3 groups of carcinomas, each characterized by specific pathological and biological profiles. The negative (NEG) group, characterized by negligible expression of both proteins, comprised small-sized, low-grade tumors associated with high contents of hormonal receptors and low growth fraction. In the NEG group, Ki-67 labelling index area (%LIa) was the only significant prognostic indicator. The P53H group, characterized by prevalence of p53 %LIa, was constituted by large-sized, high-grade tumors showing low hormonal receptor contents and high growth fraction. In the P53H group, both p53 and Ki-67 were inversely associated with both estrogen receptor (ER) and progesterone receptor (PGR), suggesting that extensive p53 immunostaining is related to poor differentiation and high proliferation. Only N status was prognostically significant in the P53H group. The P21H group, characterized by prevalence of p21(waf-1) %LIa, displayed intermediate pathological and biological features. A significant association between p53 and p21(waf-1) expression suggested functional stabilization of wtp53 and therefore possible DNA damage-dependent G1/S arrest (genetic instability) in the P21H group; P21(waf-1)expression was significantly associated with the presence of node metastasis. Patients in the P21H group had a higher recurrence rate and a shorter disease-free time interval from surgery with respect to the NEG group. Proportional hazard regression analysis disclosed Ki-67 %LIa and, to a lesser degree, PGR %LIa as significant relapse-free survival prognostic indicators.</abstract><cop>United States</cop><pmid>11241324</pmid><doi>10.1002/1097-0215(20010320)95:2<128::AID-IJC1022>3.0.CO;2-D</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Breast Neoplasms - diagnosis Breast Neoplasms - metabolism Carcinoma, Ductal, Breast - diagnosis Carcinoma, Ductal, Breast - metabolism Carcinoma, Medullary - diagnosis Carcinoma, Medullary - metabolism Cyclin-Dependent Kinase Inhibitor p21 Cyclins - biosynthesis Disease-Free Survival DNA Damage Female Humans Image Cytometry Immunohistochemistry Ki-67 Antigen - biosynthesis Lymphatic Metastasis Middle Aged Multivariate Analysis Mutation Prognosis Proportional Hazards Models Receptors, Estrogen - biosynthesis Receptors, Progesterone - biosynthesis Time Factors Tumor Suppressor Protein p53 - biosynthesis |
title | Quantitative p21(waf-1)/p53 immunohistochemical analysis defines groups of primary invasive breast carcinomas with different prognostic indicators |
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