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Epidermal growth factor receptor-negative tumors are predominantly confined to the subgroup of estradiol receptor-positive human primary breast cancers
A total of 725 human primary breast tumor biopsy samples were analyzed for epidermal growth factor receptor (EGFR) content, using a multiple-point EGFR assay standardized in accordance with the recommendations of the European Organization for Research and Treatment of Cancer Receptor Study Group. Af...
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Published in: | Cancer research (Chicago, Ill.) Ill.), 1991-09, Vol.51 (17), p.4544-4548 |
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description | A total of 725 human primary breast tumor biopsy samples were analyzed for epidermal growth factor receptor (EGFR) content, using a multiple-point EGFR assay standardized in accordance with the recommendations of the European Organization for Research and Treatment of Cancer Receptor Study Group. After the establishment of a lower cell membrane protein threshold of 0.2 mg of membrane protein per ml of assay buffer, the results of 27% (194 samples) of the EGFR determinations were excluded from the study because of insufficient assay membrane protein content. Of the remaining 531 breast tumor biopsy samples, 57% (302 samples) were shown to be EGFR positive by Scatchard analysis, with a median value of 40 fmol/mg of membrane protein. Of the breast tumor biopsy samples, 72% (380 samples) were estrogen receptor (ER) positive, and 65% (344 samples) were progesterone receptor (PgR) positive. EGFR positivity was found in 46% (173 of 380) of ER-positive and in 85% (129 of 151) of ER-negative breast tumor biopsy samples (P less than 0.0001), as well as in 49% (168 of 344) of PgR-positive and in 72% (134 of 186) of PgR-negative breast tumor biopsy samples (P less than 0.0001). Mean EGFR levels in ER-positive breast tumor biopsy samples were lower than they were in ER-negative ones, 40 +/- 31 (SD) against 72 +/- 55 fmol/mg of membrane protein (P less than 0.0001). Similarly, mean EGFR levels in PgR-positive breast tumor biopsy samples were lower than they were in PgR-negative ones, 41 +/- 29 against 70 +/- 56 fmol/mg of membrane protein (P less than 0.0001). Both EGFR positivity and EGFR levels decreased with increasing steroid hormone receptor levels. A multivariate analysis showed only ER to be independently associated with EGFR. |
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G ; BEEX, L. V. A. M ; GEURTS-MOESPOT, A ; HEUVEL, J. J. T. M ; KIENHUIS, C. B. M ; BENRAAD, T. J</creator><creatorcontrib>KOENDERS, P. G ; BEEX, L. V. A. M ; GEURTS-MOESPOT, A ; HEUVEL, J. J. T. M ; KIENHUIS, C. B. M ; BENRAAD, T. J</creatorcontrib><description>A total of 725 human primary breast tumor biopsy samples were analyzed for epidermal growth factor receptor (EGFR) content, using a multiple-point EGFR assay standardized in accordance with the recommendations of the European Organization for Research and Treatment of Cancer Receptor Study Group. After the establishment of a lower cell membrane protein threshold of 0.2 mg of membrane protein per ml of assay buffer, the results of 27% (194 samples) of the EGFR determinations were excluded from the study because of insufficient assay membrane protein content. Of the remaining 531 breast tumor biopsy samples, 57% (302 samples) were shown to be EGFR positive by Scatchard analysis, with a median value of 40 fmol/mg of membrane protein. Of the breast tumor biopsy samples, 72% (380 samples) were estrogen receptor (ER) positive, and 65% (344 samples) were progesterone receptor (PgR) positive. EGFR positivity was found in 46% (173 of 380) of ER-positive and in 85% (129 of 151) of ER-negative breast tumor biopsy samples (P less than 0.0001), as well as in 49% (168 of 344) of PgR-positive and in 72% (134 of 186) of PgR-negative breast tumor biopsy samples (P less than 0.0001). Mean EGFR levels in ER-positive breast tumor biopsy samples were lower than they were in ER-negative ones, 40 +/- 31 (SD) against 72 +/- 55 fmol/mg of membrane protein (P less than 0.0001). Similarly, mean EGFR levels in PgR-positive breast tumor biopsy samples were lower than they were in PgR-negative ones, 41 +/- 29 against 70 +/- 56 fmol/mg of membrane protein (P less than 0.0001). Both EGFR positivity and EGFR levels decreased with increasing steroid hormone receptor levels. A multivariate analysis showed only ER to be independently associated with EGFR.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 1873798</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Biological and medical sciences ; Biomarkers, Tumor - analysis ; Breast Neoplasms - chemistry ; Cryopreservation ; epidermal growth factor ; estradiol ; Gynecology. Andrology. Obstetrics ; Humans ; Mammary gland diseases ; Medical sciences ; Prognosis ; Receptor, Epidermal Growth Factor - analysis ; Receptors, Estradiol - analysis ; Receptors, Progesterone - analysis ; Time Factors ; Tissue Preservation ; Tumors</subject><ispartof>Cancer research (Chicago, Ill.), 1991-09, Vol.51 (17), p.4544-4548</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4985152$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1873798$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KOENDERS, P. G</creatorcontrib><creatorcontrib>BEEX, L. V. A. M</creatorcontrib><creatorcontrib>GEURTS-MOESPOT, A</creatorcontrib><creatorcontrib>HEUVEL, J. J. T. M</creatorcontrib><creatorcontrib>KIENHUIS, C. B. M</creatorcontrib><creatorcontrib>BENRAAD, T. J</creatorcontrib><title>Epidermal growth factor receptor-negative tumors are predominantly confined to the subgroup of estradiol receptor-positive human primary breast cancers</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>A total of 725 human primary breast tumor biopsy samples were analyzed for epidermal growth factor receptor (EGFR) content, using a multiple-point EGFR assay standardized in accordance with the recommendations of the European Organization for Research and Treatment of Cancer Receptor Study Group. After the establishment of a lower cell membrane protein threshold of 0.2 mg of membrane protein per ml of assay buffer, the results of 27% (194 samples) of the EGFR determinations were excluded from the study because of insufficient assay membrane protein content. Of the remaining 531 breast tumor biopsy samples, 57% (302 samples) were shown to be EGFR positive by Scatchard analysis, with a median value of 40 fmol/mg of membrane protein. Of the breast tumor biopsy samples, 72% (380 samples) were estrogen receptor (ER) positive, and 65% (344 samples) were progesterone receptor (PgR) positive. EGFR positivity was found in 46% (173 of 380) of ER-positive and in 85% (129 of 151) of ER-negative breast tumor biopsy samples (P less than 0.0001), as well as in 49% (168 of 344) of PgR-positive and in 72% (134 of 186) of PgR-negative breast tumor biopsy samples (P less than 0.0001). Mean EGFR levels in ER-positive breast tumor biopsy samples were lower than they were in ER-negative ones, 40 +/- 31 (SD) against 72 +/- 55 fmol/mg of membrane protein (P less than 0.0001). Similarly, mean EGFR levels in PgR-positive breast tumor biopsy samples were lower than they were in PgR-negative ones, 41 +/- 29 against 70 +/- 56 fmol/mg of membrane protein (P less than 0.0001). Both EGFR positivity and EGFR levels decreased with increasing steroid hormone receptor levels. A multivariate analysis showed only ER to be independently associated with EGFR.</description><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Breast Neoplasms - chemistry</subject><subject>Cryopreservation</subject><subject>epidermal growth factor</subject><subject>estradiol</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Mammary gland diseases</subject><subject>Medical sciences</subject><subject>Prognosis</subject><subject>Receptor, Epidermal Growth Factor - analysis</subject><subject>Receptors, Estradiol - analysis</subject><subject>Receptors, Progesterone - analysis</subject><subject>Time Factors</subject><subject>Tissue Preservation</subject><subject>Tumors</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><recordid>eNqFkM9KxDAQh4so67r6CEIO4q2QNskmPcqy_gHBi57LJJ3sRtqmJqmyT-LrWrTo0dPMMB8f85ujbFkIpnLJuTjOlpRSlQsuy9PsLMbXaRQFFYtsUSjJZKWW2ed2cA2GDlqyC_4j7YkFk3wgAQ0OU5P3uIPk3pGksfMhEghIhoCN71wPfWoPxPjeuh4bkjxJeyRx1JNrHIi3BGMK0Djf_gkHH923cD920E8u10E4EB0QYiIGeoMhnmcnFtqIF3NdZS-32-fNff74dPewuXnM94zSlMuqoZppqLiWlShKqUCjqOzaaEmFpBQstxWnpaWN1nxNS4aKGaq0UQKFZqvs-sc7BP82TtfWnYsG2xZ69GOsZUk5Z0z8CxbrYl3xgk7g5QyOusOmnvPV88un_dW8h2igtWEK7OIvxislClGyL91-jyM</recordid><startdate>19910901</startdate><enddate>19910901</enddate><creator>KOENDERS, P. G</creator><creator>BEEX, L. V. A. M</creator><creator>GEURTS-MOESPOT, A</creator><creator>HEUVEL, J. J. T. M</creator><creator>KIENHUIS, C. B. M</creator><creator>BENRAAD, T. J</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19910901</creationdate><title>Epidermal growth factor receptor-negative tumors are predominantly confined to the subgroup of estradiol receptor-positive human primary breast cancers</title><author>KOENDERS, P. G ; BEEX, L. V. A. M ; GEURTS-MOESPOT, A ; HEUVEL, J. J. T. M ; KIENHUIS, C. B. M ; BENRAAD, T. J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h300t-79d0b3ba94b7951278abe59f6cb705700af4f9402f0dbb46023e83c08bc85e5b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Breast Neoplasms - chemistry</topic><topic>Cryopreservation</topic><topic>epidermal growth factor</topic><topic>estradiol</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Mammary gland diseases</topic><topic>Medical sciences</topic><topic>Prognosis</topic><topic>Receptor, Epidermal Growth Factor - analysis</topic><topic>Receptors, Estradiol - analysis</topic><topic>Receptors, Progesterone - analysis</topic><topic>Time Factors</topic><topic>Tissue Preservation</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KOENDERS, P. G</creatorcontrib><creatorcontrib>BEEX, L. V. A. M</creatorcontrib><creatorcontrib>GEURTS-MOESPOT, A</creatorcontrib><creatorcontrib>HEUVEL, J. J. T. M</creatorcontrib><creatorcontrib>KIENHUIS, C. B. M</creatorcontrib><creatorcontrib>BENRAAD, T. J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KOENDERS, P. G</au><au>BEEX, L. V. A. M</au><au>GEURTS-MOESPOT, A</au><au>HEUVEL, J. J. T. M</au><au>KIENHUIS, C. B. M</au><au>BENRAAD, T. J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Epidermal growth factor receptor-negative tumors are predominantly confined to the subgroup of estradiol receptor-positive human primary breast cancers</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1991-09-01</date><risdate>1991</risdate><volume>51</volume><issue>17</issue><spage>4544</spage><epage>4548</epage><pages>4544-4548</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>A total of 725 human primary breast tumor biopsy samples were analyzed for epidermal growth factor receptor (EGFR) content, using a multiple-point EGFR assay standardized in accordance with the recommendations of the European Organization for Research and Treatment of Cancer Receptor Study Group. After the establishment of a lower cell membrane protein threshold of 0.2 mg of membrane protein per ml of assay buffer, the results of 27% (194 samples) of the EGFR determinations were excluded from the study because of insufficient assay membrane protein content. Of the remaining 531 breast tumor biopsy samples, 57% (302 samples) were shown to be EGFR positive by Scatchard analysis, with a median value of 40 fmol/mg of membrane protein. Of the breast tumor biopsy samples, 72% (380 samples) were estrogen receptor (ER) positive, and 65% (344 samples) were progesterone receptor (PgR) positive. EGFR positivity was found in 46% (173 of 380) of ER-positive and in 85% (129 of 151) of ER-negative breast tumor biopsy samples (P less than 0.0001), as well as in 49% (168 of 344) of PgR-positive and in 72% (134 of 186) of PgR-negative breast tumor biopsy samples (P less than 0.0001). Mean EGFR levels in ER-positive breast tumor biopsy samples were lower than they were in ER-negative ones, 40 +/- 31 (SD) against 72 +/- 55 fmol/mg of membrane protein (P less than 0.0001). Similarly, mean EGFR levels in PgR-positive breast tumor biopsy samples were lower than they were in PgR-negative ones, 41 +/- 29 against 70 +/- 56 fmol/mg of membrane protein (P less than 0.0001). Both EGFR positivity and EGFR levels decreased with increasing steroid hormone receptor levels. A multivariate analysis showed only ER to be independently associated with EGFR.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>1873798</pmid><tpages>5</tpages></addata></record> |
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subjects | Biological and medical sciences Biomarkers, Tumor - analysis Breast Neoplasms - chemistry Cryopreservation epidermal growth factor estradiol Gynecology. Andrology. Obstetrics Humans Mammary gland diseases Medical sciences Prognosis Receptor, Epidermal Growth Factor - analysis Receptors, Estradiol - analysis Receptors, Progesterone - analysis Time Factors Tissue Preservation Tumors |
title | Epidermal growth factor receptor-negative tumors are predominantly confined to the subgroup of estradiol receptor-positive human primary breast cancers |
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