p53 protein and vimentin in invasive ductal NOS breast carcinoma--relationship with survival and sites of metastases

p53 protein and vimentin status were available from immunocytochemical studies of 253 formalin-fixed paraffin-embedded invasive ductal not otherwise specified (NOS) carcinomas from patients for whom follow-up data was also on file. For the 127 node-negative patients, multivariate analysis showed a h...

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Veröffentlicht in:European journal of cancer (1990) 1994, Vol.30A (10), p.1527-1534
Hauptverfasser: Domagala, W, Striker, G, Szadowska, A, Dukowicz, A, Harezga, B, Osborn, M
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container_end_page 1534
container_issue 10
container_start_page 1527
container_title European journal of cancer (1990)
container_volume 30A
creator Domagala, W
Striker, G
Szadowska, A
Dukowicz, A
Harezga, B
Osborn, M
description p53 protein and vimentin status were available from immunocytochemical studies of 253 formalin-fixed paraffin-embedded invasive ductal not otherwise specified (NOS) carcinomas from patients for whom follow-up data was also on file. For the 127 node-negative patients, multivariate analysis showed a highly significant correlation between p53 and vimentin (P < 0.001), a strong correlation between vimentin and probability of survival to 90 months but only a weak association between p53 and survival to 90 months. p53 also never entered trees of prognostic indicators derived using stepwise regression with Kaplan-Meier statistics for node-negative and node-positive subgroups, while vimentin status dominated the node-negative trunk. In addition, p53 and vimentin status were analysed versus the site of the first distant metastasis for node-negative and node-positive patients. Analysis by p53 status showed no significant effect on visceral metastases. In contrast, vimentin-positive primaries metastasised twice (and in node-negative patients, 3.5 times) as often to lung, liver and brain as did the vimentin-negative primaries. Both p53-positive and vimentin-positive tumours showed a significantly lower tendency to metastasise to the bone than did their negative counterparts.
doi_str_mv 10.1016/0959-8049(94)00288-G
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For the 127 node-negative patients, multivariate analysis showed a highly significant correlation between p53 and vimentin (P &lt; 0.001), a strong correlation between vimentin and probability of survival to 90 months but only a weak association between p53 and survival to 90 months. p53 also never entered trees of prognostic indicators derived using stepwise regression with Kaplan-Meier statistics for node-negative and node-positive subgroups, while vimentin status dominated the node-negative trunk. In addition, p53 and vimentin status were analysed versus the site of the first distant metastasis for node-negative and node-positive patients. Analysis by p53 status showed no significant effect on visceral metastases. In contrast, vimentin-positive primaries metastasised twice (and in node-negative patients, 3.5 times) as often to lung, liver and brain as did the vimentin-negative primaries. Both p53-positive and vimentin-positive tumours showed a significantly lower tendency to metastasise to the bone than did their negative counterparts.</description><identifier>ISSN: 0959-8049</identifier><identifier>DOI: 10.1016/0959-8049(94)00288-G</identifier><identifier>PMID: 7833113</identifier><language>eng</language><publisher>England</publisher><subject>Adult ; Biomarkers, Tumor - analysis ; Breast Neoplasms - chemistry ; Breast Neoplasms - mortality ; Carcinoma, Ductal, Breast - chemistry ; Carcinoma, Ductal, Breast - mortality ; Carcinoma, Ductal, Breast - secondary ; Female ; Follow-Up Studies ; Humans ; Lymphatic Metastasis ; Middle Aged ; Neoplasm Proteins - analysis ; Prognosis ; Tumor Suppressor Protein p53 - analysis ; Vimentin - analysis</subject><ispartof>European journal of cancer (1990), 1994, Vol.30A (10), p.1527-1534</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,4012,27910,27911,27912</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7833113$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Domagala, W</creatorcontrib><creatorcontrib>Striker, G</creatorcontrib><creatorcontrib>Szadowska, A</creatorcontrib><creatorcontrib>Dukowicz, A</creatorcontrib><creatorcontrib>Harezga, B</creatorcontrib><creatorcontrib>Osborn, M</creatorcontrib><title>p53 protein and vimentin in invasive ductal NOS breast carcinoma--relationship with survival and sites of metastases</title><title>European journal of cancer (1990)</title><addtitle>Eur J Cancer</addtitle><description>p53 protein and vimentin status were available from immunocytochemical studies of 253 formalin-fixed paraffin-embedded invasive ductal not otherwise specified (NOS) carcinomas from patients for whom follow-up data was also on file. 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Both p53-positive and vimentin-positive tumours showed a significantly lower tendency to metastasise to the bone than did their negative counterparts.</description><subject>Adult</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Breast Neoplasms - chemistry</subject><subject>Breast Neoplasms - mortality</subject><subject>Carcinoma, Ductal, Breast - chemistry</subject><subject>Carcinoma, Ductal, Breast - mortality</subject><subject>Carcinoma, Ductal, Breast - secondary</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Lymphatic Metastasis</subject><subject>Middle Aged</subject><subject>Neoplasm Proteins - analysis</subject><subject>Prognosis</subject><subject>Tumor Suppressor Protein p53 - analysis</subject><subject>Vimentin - analysis</subject><issn>0959-8049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE9LAzEQxXNQaq1-A4WcRA-rkyabTY5SahWKPdj7kk1maWT_ucmu-O1dtQgDj3n83oMZQq4Y3DNg8gF0qhMFQt9qcQewVCrZnJD5v31GzkN4B4BMCZiRWaY4Z4zPSexSTru-jegbahpHR19jE6fld0YT_IjUDTaair7u3mjRowmRWtNb37S1SZIeKxN924SD7-injwcahn704xT4KQw-YqBtSWuMU9IEDBfktDRVwMujLsj-ab1fPSfb3eZl9bhNOsZVTIQrlqWTkmswDoQqBCwzsCkzlgktndJYWOkAjJapkYXmtgREKbKSpaLkC3LzVzvd9zFgiHntg8WqMg22Q8izTGommZrA6yM4FDW6vOt9bfqv_Pgl_g3UYGoG</recordid><startdate>1994</startdate><enddate>1994</enddate><creator>Domagala, W</creator><creator>Striker, G</creator><creator>Szadowska, A</creator><creator>Dukowicz, A</creator><creator>Harezga, B</creator><creator>Osborn, M</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>1994</creationdate><title>p53 protein and vimentin in invasive ductal NOS breast carcinoma--relationship with survival and sites of metastases</title><author>Domagala, W ; Striker, G ; Szadowska, A ; Dukowicz, A ; Harezga, B ; Osborn, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p138t-4db2fd66390ad048b40270c51ac1496d89ebc6d00a965a6b93cf0ee647f154f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Adult</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Breast Neoplasms - chemistry</topic><topic>Breast Neoplasms - mortality</topic><topic>Carcinoma, Ductal, Breast - chemistry</topic><topic>Carcinoma, Ductal, Breast - mortality</topic><topic>Carcinoma, Ductal, Breast - secondary</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Lymphatic Metastasis</topic><topic>Middle Aged</topic><topic>Neoplasm Proteins - analysis</topic><topic>Prognosis</topic><topic>Tumor Suppressor Protein p53 - analysis</topic><topic>Vimentin - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Domagala, W</creatorcontrib><creatorcontrib>Striker, G</creatorcontrib><creatorcontrib>Szadowska, A</creatorcontrib><creatorcontrib>Dukowicz, A</creatorcontrib><creatorcontrib>Harezga, B</creatorcontrib><creatorcontrib>Osborn, M</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>European journal of cancer (1990)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Domagala, W</au><au>Striker, G</au><au>Szadowska, A</au><au>Dukowicz, A</au><au>Harezga, B</au><au>Osborn, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>p53 protein and vimentin in invasive ductal NOS breast carcinoma--relationship with survival and sites of metastases</atitle><jtitle>European journal of cancer (1990)</jtitle><addtitle>Eur J Cancer</addtitle><date>1994</date><risdate>1994</risdate><volume>30A</volume><issue>10</issue><spage>1527</spage><epage>1534</epage><pages>1527-1534</pages><issn>0959-8049</issn><abstract>p53 protein and vimentin status were available from immunocytochemical studies of 253 formalin-fixed paraffin-embedded invasive ductal not otherwise specified (NOS) carcinomas from patients for whom follow-up data was also on file. For the 127 node-negative patients, multivariate analysis showed a highly significant correlation between p53 and vimentin (P &lt; 0.001), a strong correlation between vimentin and probability of survival to 90 months but only a weak association between p53 and survival to 90 months. p53 also never entered trees of prognostic indicators derived using stepwise regression with Kaplan-Meier statistics for node-negative and node-positive subgroups, while vimentin status dominated the node-negative trunk. In addition, p53 and vimentin status were analysed versus the site of the first distant metastasis for node-negative and node-positive patients. Analysis by p53 status showed no significant effect on visceral metastases. In contrast, vimentin-positive primaries metastasised twice (and in node-negative patients, 3.5 times) as often to lung, liver and brain as did the vimentin-negative primaries. Both p53-positive and vimentin-positive tumours showed a significantly lower tendency to metastasise to the bone than did their negative counterparts.</abstract><cop>England</cop><pmid>7833113</pmid><doi>10.1016/0959-8049(94)00288-G</doi><tpages>8</tpages></addata></record>
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Adult
Biomarkers, Tumor - analysis
Breast Neoplasms - chemistry
Breast Neoplasms - mortality
Carcinoma, Ductal, Breast - chemistry
Carcinoma, Ductal, Breast - mortality
Carcinoma, Ductal, Breast - secondary
Female
Follow-Up Studies
Humans
Lymphatic Metastasis
Middle Aged
Neoplasm Proteins - analysis
Prognosis
Tumor Suppressor Protein p53 - analysis
Vimentin - analysis
title p53 protein and vimentin in invasive ductal NOS breast carcinoma--relationship with survival and sites of metastases
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