Loading…

Expression of chemerin correlates with a poor prognosis in female breast cancer patients

Chemerin was reported to regulate adipogenesis, metabolism, and immunity. But, its relation to cancer remains controversial. In breast cancer, chemerin expression has only been studied in serum, however, its expression in tissue, to our knowledge, has not been studied. The aim of this study was to i...

Full description

Saved in:
Bibliographic Details
Published in:Breast cancer targets and therapy 2018-01, Vol.10, p.169-176
Main Authors: El-Sagheer, Ghada, Gayyed, Mariana, Ahmad, Asmaa, Abd El-Fattah, Aliaa, Mohamed, Manar
Format: Article
Language:English
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c619t-6618c2cbc31e6af75d6de9861acae49e069263e6893546274e8bc192b177865d3
cites
container_end_page 176
container_issue
container_start_page 169
container_title Breast cancer targets and therapy
container_volume 10
creator El-Sagheer, Ghada
Gayyed, Mariana
Ahmad, Asmaa
Abd El-Fattah, Aliaa
Mohamed, Manar
description Chemerin was reported to regulate adipogenesis, metabolism, and immunity. But, its relation to cancer remains controversial. In breast cancer, chemerin expression has only been studied in serum, however, its expression in tissue, to our knowledge, has not been studied. The aim of this study was to investigate chemerin expression in breast cancer tissue in comparison to the adjacent normal tissue, and to assess its relationship to disease prognosis. We examined chemerin expression in tissue with immunohistochemistry and analyzed the association of chemerin expression with the patients' clinical and pathological characteristics to determine its role as a predictor of the disease and its relation to disease prognosis. We detected a significantly higher expression of chemerin in the malignant vs the non-cancerous tissue specimens in 30/53, (56%) patients, ( =0.001). Moreover, its expression was significantly higher in the metastatic lymph nodes in comparison to the tumor tissues, ( =0.01). Chemerin expression was significantly correlated with weight ( =0.256, =0.04), body mass index ( =0.233, =0.03), tumor size ( =0.235, =0.03), lymph node metastasis ( =0.265, =0.045), distant metastasis ( =0.267, =0.02), and tumor grading, ( =0.421, =0.004), while it was inversely significantly correlated with estrogen receptor and progesterone receptor expression in malignant breast tissues ( =0.038, =-0.437, and =0.047, =-0.316), respectively. The area under the receiver operating characteristic curve for chemerin as a predictor of breast cancer was 0.82, (
doi_str_mv 10.2147/BCTT.S178181
format article
fullrecord <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_932c9aa9bda34255a3a7e4658495d33c</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A574315023</galeid><doaj_id>oai_doaj_org_article_932c9aa9bda34255a3a7e4658495d33c</doaj_id><sourcerecordid>A574315023</sourcerecordid><originalsourceid>FETCH-LOGICAL-c619t-6618c2cbc31e6af75d6de9861acae49e069263e6893546274e8bc192b177865d3</originalsourceid><addsrcrecordid>eNptkk1v1DAQhiMEolXpjTOKhIQ4sEv8EX9ckMqqQKVKHFgkbtbEmWy8SuJgJ9D-e7zsUnYR9sHW-JnXmncmy56TYkkJl2_fr9br5RciFVHkUXZOiNQLwgh_fHQ_yy5j3Ba7JQvO5dPsjBVcKybJefbt-m4MGKPzQ-6b3LbYY3BDbn0I2MGEMf_ppjaHfPQ-5GPwm8FHF_PENNhDh3kVEOKUWxgsJgImh8MUn2VPGugiXh7Oi-zrh-v16tPi9vPHm9XV7cIKoqeFEERZaivLCApoZFmLGrUSBCwg11gITQVDoTQruaCSo6os0bQiUipR1uwiu9nr1h62Zgyuh3BvPDjzO-DDxkCYnO3QaEatBtBVDYzTsgQGErkoFddJiNmk9W6vNc5Vj7VNdQToTkRPXwbXmo3_YQQtJFMkCbw-CAT_fcY4md5Fi10HA_o5mtQzUjCudZnQl_-gWz-HIVllKKU8NUsJ9ZfaJKeNGxqf_rU7UXNVSs5IWVCWqOV_qLRr7J31AzYuxU8SXh0ltAjd1EbfzVMag3gKvtmDNvgYAzYPZpBiV400uwk0hwlM-ItjAx_gP_PGfgE2r9Nx</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2224000868</pqid></control><display><type>article</type><title>Expression of chemerin correlates with a poor prognosis in female breast cancer patients</title><source>Publicly Available Content Database</source><source>Taylor &amp; Francis Open Access Journals</source><source>PubMed Central</source><creator>El-Sagheer, Ghada ; Gayyed, Mariana ; Ahmad, Asmaa ; Abd El-Fattah, Aliaa ; Mohamed, Manar</creator><creatorcontrib>El-Sagheer, Ghada ; Gayyed, Mariana ; Ahmad, Asmaa ; Abd El-Fattah, Aliaa ; Mohamed, Manar</creatorcontrib><description>Chemerin was reported to regulate adipogenesis, metabolism, and immunity. But, its relation to cancer remains controversial. In breast cancer, chemerin expression has only been studied in serum, however, its expression in tissue, to our knowledge, has not been studied. The aim of this study was to investigate chemerin expression in breast cancer tissue in comparison to the adjacent normal tissue, and to assess its relationship to disease prognosis. We examined chemerin expression in tissue with immunohistochemistry and analyzed the association of chemerin expression with the patients' clinical and pathological characteristics to determine its role as a predictor of the disease and its relation to disease prognosis. We detected a significantly higher expression of chemerin in the malignant vs the non-cancerous tissue specimens in 30/53, (56%) patients, ( =0.001). Moreover, its expression was significantly higher in the metastatic lymph nodes in comparison to the tumor tissues, ( =0.01). Chemerin expression was significantly correlated with weight ( =0.256, =0.04), body mass index ( =0.233, =0.03), tumor size ( =0.235, =0.03), lymph node metastasis ( =0.265, =0.045), distant metastasis ( =0.267, =0.02), and tumor grading, ( =0.421, =0.004), while it was inversely significantly correlated with estrogen receptor and progesterone receptor expression in malignant breast tissues ( =0.038, =-0.437, and =0.047, =-0.316), respectively. The area under the receiver operating characteristic curve for chemerin as a predictor of breast cancer was 0.82, ( &lt;0.001, sensitivity 89%, and specificity 69%). The Kaplan-Meier survival curves revealed that patients with higher chemerin expression had worse overall survival in comparison to those with a lower chemerin expression, ( =0.001). Our results revealed higher chemerin expression in malignant vs adjacent normal breast tissue and lend support to a presumable role of chemerin tissue expression as an independent predictor of poor prognosis in breast cancer patients.</description><identifier>ISSN: 1179-1314</identifier><identifier>EISSN: 1179-1314</identifier><identifier>DOI: 10.2147/BCTT.S178181</identifier><identifier>PMID: 30498371</identifier><language>eng</language><publisher>New Zealand: Dove Medical Press Limited</publisher><subject>adipocyte development ; Adipocytes ; Analysis ; Angiogenesis ; Body mass index ; Breast cancer ; Cancer metastasis ; Cancer patients ; Cancer research ; chemerin expression ; Development and progression ; Disease ; Esophagus ; Estrogens ; Family medical history ; Gene expression ; Genetic aspects ; Health aspects ; Immunohistochemistry ; Inflammation ; Insulin ; Insulin-like growth factors ; Internal medicine ; Ligands ; Lung cancer ; Medical research ; Medicine ; Melanoma ; Metabolic syndrome ; Obesity ; Original Research ; Phenols (Class of compounds) ; Progesterone ; Prognosis ; Sex hormones ; Tumor necrosis factor-TNF ; Tumors ; Women's health</subject><ispartof>Breast cancer targets and therapy, 2018-01, Vol.10, p.169-176</ispartof><rights>COPYRIGHT 2018 Dove Medical Press Limited</rights><rights>2018. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2018 El-Sagheer et al. This work is published and licensed by Dove Medical Press Limited 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c619t-6618c2cbc31e6af75d6de9861acae49e069263e6893546274e8bc192b177865d3</citedby><orcidid>0000-0001-8769-5199</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2224000868/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2224000868?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25744,27915,27916,37003,37004,44581,53782,53784,74887</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30498371$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>El-Sagheer, Ghada</creatorcontrib><creatorcontrib>Gayyed, Mariana</creatorcontrib><creatorcontrib>Ahmad, Asmaa</creatorcontrib><creatorcontrib>Abd El-Fattah, Aliaa</creatorcontrib><creatorcontrib>Mohamed, Manar</creatorcontrib><title>Expression of chemerin correlates with a poor prognosis in female breast cancer patients</title><title>Breast cancer targets and therapy</title><addtitle>Breast Cancer (Dove Med Press)</addtitle><description>Chemerin was reported to regulate adipogenesis, metabolism, and immunity. But, its relation to cancer remains controversial. In breast cancer, chemerin expression has only been studied in serum, however, its expression in tissue, to our knowledge, has not been studied. The aim of this study was to investigate chemerin expression in breast cancer tissue in comparison to the adjacent normal tissue, and to assess its relationship to disease prognosis. We examined chemerin expression in tissue with immunohistochemistry and analyzed the association of chemerin expression with the patients' clinical and pathological characteristics to determine its role as a predictor of the disease and its relation to disease prognosis. We detected a significantly higher expression of chemerin in the malignant vs the non-cancerous tissue specimens in 30/53, (56%) patients, ( =0.001). Moreover, its expression was significantly higher in the metastatic lymph nodes in comparison to the tumor tissues, ( =0.01). Chemerin expression was significantly correlated with weight ( =0.256, =0.04), body mass index ( =0.233, =0.03), tumor size ( =0.235, =0.03), lymph node metastasis ( =0.265, =0.045), distant metastasis ( =0.267, =0.02), and tumor grading, ( =0.421, =0.004), while it was inversely significantly correlated with estrogen receptor and progesterone receptor expression in malignant breast tissues ( =0.038, =-0.437, and =0.047, =-0.316), respectively. The area under the receiver operating characteristic curve for chemerin as a predictor of breast cancer was 0.82, ( &lt;0.001, sensitivity 89%, and specificity 69%). The Kaplan-Meier survival curves revealed that patients with higher chemerin expression had worse overall survival in comparison to those with a lower chemerin expression, ( =0.001). Our results revealed higher chemerin expression in malignant vs adjacent normal breast tissue and lend support to a presumable role of chemerin tissue expression as an independent predictor of poor prognosis in breast cancer patients.</description><subject>adipocyte development</subject><subject>Adipocytes</subject><subject>Analysis</subject><subject>Angiogenesis</subject><subject>Body mass index</subject><subject>Breast cancer</subject><subject>Cancer metastasis</subject><subject>Cancer patients</subject><subject>Cancer research</subject><subject>chemerin expression</subject><subject>Development and progression</subject><subject>Disease</subject><subject>Esophagus</subject><subject>Estrogens</subject><subject>Family medical history</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Immunohistochemistry</subject><subject>Inflammation</subject><subject>Insulin</subject><subject>Insulin-like growth factors</subject><subject>Internal medicine</subject><subject>Ligands</subject><subject>Lung cancer</subject><subject>Medical research</subject><subject>Medicine</subject><subject>Melanoma</subject><subject>Metabolic syndrome</subject><subject>Obesity</subject><subject>Original Research</subject><subject>Phenols (Class of compounds)</subject><subject>Progesterone</subject><subject>Prognosis</subject><subject>Sex hormones</subject><subject>Tumor necrosis factor-TNF</subject><subject>Tumors</subject><subject>Women's health</subject><issn>1179-1314</issn><issn>1179-1314</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkk1v1DAQhiMEolXpjTOKhIQ4sEv8EX9ckMqqQKVKHFgkbtbEmWy8SuJgJ9D-e7zsUnYR9sHW-JnXmncmy56TYkkJl2_fr9br5RciFVHkUXZOiNQLwgh_fHQ_yy5j3Ba7JQvO5dPsjBVcKybJefbt-m4MGKPzQ-6b3LbYY3BDbn0I2MGEMf_ppjaHfPQ-5GPwm8FHF_PENNhDh3kVEOKUWxgsJgImh8MUn2VPGugiXh7Oi-zrh-v16tPi9vPHm9XV7cIKoqeFEERZaivLCApoZFmLGrUSBCwg11gITQVDoTQruaCSo6os0bQiUipR1uwiu9nr1h62Zgyuh3BvPDjzO-DDxkCYnO3QaEatBtBVDYzTsgQGErkoFddJiNmk9W6vNc5Vj7VNdQToTkRPXwbXmo3_YQQtJFMkCbw-CAT_fcY4md5Fi10HA_o5mtQzUjCudZnQl_-gWz-HIVllKKU8NUsJ9ZfaJKeNGxqf_rU7UXNVSs5IWVCWqOV_qLRr7J31AzYuxU8SXh0ltAjd1EbfzVMag3gKvtmDNvgYAzYPZpBiV400uwk0hwlM-ItjAx_gP_PGfgE2r9Nx</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>El-Sagheer, Ghada</creator><creator>Gayyed, Mariana</creator><creator>Ahmad, Asmaa</creator><creator>Abd El-Fattah, Aliaa</creator><creator>Mohamed, Manar</creator><general>Dove Medical Press Limited</general><general>Taylor &amp; Francis Ltd</general><general>Dove Medical Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-8769-5199</orcidid></search><sort><creationdate>20180101</creationdate><title>Expression of chemerin correlates with a poor prognosis in female breast cancer patients</title><author>El-Sagheer, Ghada ; Gayyed, Mariana ; Ahmad, Asmaa ; Abd El-Fattah, Aliaa ; Mohamed, Manar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c619t-6618c2cbc31e6af75d6de9861acae49e069263e6893546274e8bc192b177865d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>adipocyte development</topic><topic>Adipocytes</topic><topic>Analysis</topic><topic>Angiogenesis</topic><topic>Body mass index</topic><topic>Breast cancer</topic><topic>Cancer metastasis</topic><topic>Cancer patients</topic><topic>Cancer research</topic><topic>chemerin expression</topic><topic>Development and progression</topic><topic>Disease</topic><topic>Esophagus</topic><topic>Estrogens</topic><topic>Family medical history</topic><topic>Gene expression</topic><topic>Genetic aspects</topic><topic>Health aspects</topic><topic>Immunohistochemistry</topic><topic>Inflammation</topic><topic>Insulin</topic><topic>Insulin-like growth factors</topic><topic>Internal medicine</topic><topic>Ligands</topic><topic>Lung cancer</topic><topic>Medical research</topic><topic>Medicine</topic><topic>Melanoma</topic><topic>Metabolic syndrome</topic><topic>Obesity</topic><topic>Original Research</topic><topic>Phenols (Class of compounds)</topic><topic>Progesterone</topic><topic>Prognosis</topic><topic>Sex hormones</topic><topic>Tumor necrosis factor-TNF</topic><topic>Tumors</topic><topic>Women's health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>El-Sagheer, Ghada</creatorcontrib><creatorcontrib>Gayyed, Mariana</creatorcontrib><creatorcontrib>Ahmad, Asmaa</creatorcontrib><creatorcontrib>Abd El-Fattah, Aliaa</creatorcontrib><creatorcontrib>Mohamed, Manar</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Breast cancer targets and therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>El-Sagheer, Ghada</au><au>Gayyed, Mariana</au><au>Ahmad, Asmaa</au><au>Abd El-Fattah, Aliaa</au><au>Mohamed, Manar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of chemerin correlates with a poor prognosis in female breast cancer patients</atitle><jtitle>Breast cancer targets and therapy</jtitle><addtitle>Breast Cancer (Dove Med Press)</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>10</volume><spage>169</spage><epage>176</epage><pages>169-176</pages><issn>1179-1314</issn><eissn>1179-1314</eissn><abstract>Chemerin was reported to regulate adipogenesis, metabolism, and immunity. But, its relation to cancer remains controversial. In breast cancer, chemerin expression has only been studied in serum, however, its expression in tissue, to our knowledge, has not been studied. The aim of this study was to investigate chemerin expression in breast cancer tissue in comparison to the adjacent normal tissue, and to assess its relationship to disease prognosis. We examined chemerin expression in tissue with immunohistochemistry and analyzed the association of chemerin expression with the patients' clinical and pathological characteristics to determine its role as a predictor of the disease and its relation to disease prognosis. We detected a significantly higher expression of chemerin in the malignant vs the non-cancerous tissue specimens in 30/53, (56%) patients, ( =0.001). Moreover, its expression was significantly higher in the metastatic lymph nodes in comparison to the tumor tissues, ( =0.01). Chemerin expression was significantly correlated with weight ( =0.256, =0.04), body mass index ( =0.233, =0.03), tumor size ( =0.235, =0.03), lymph node metastasis ( =0.265, =0.045), distant metastasis ( =0.267, =0.02), and tumor grading, ( =0.421, =0.004), while it was inversely significantly correlated with estrogen receptor and progesterone receptor expression in malignant breast tissues ( =0.038, =-0.437, and =0.047, =-0.316), respectively. The area under the receiver operating characteristic curve for chemerin as a predictor of breast cancer was 0.82, ( &lt;0.001, sensitivity 89%, and specificity 69%). The Kaplan-Meier survival curves revealed that patients with higher chemerin expression had worse overall survival in comparison to those with a lower chemerin expression, ( =0.001). Our results revealed higher chemerin expression in malignant vs adjacent normal breast tissue and lend support to a presumable role of chemerin tissue expression as an independent predictor of poor prognosis in breast cancer patients.</abstract><cop>New Zealand</cop><pub>Dove Medical Press Limited</pub><pmid>30498371</pmid><doi>10.2147/BCTT.S178181</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-8769-5199</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1179-1314
ispartof Breast cancer targets and therapy, 2018-01, Vol.10, p.169-176
issn 1179-1314
1179-1314
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_932c9aa9bda34255a3a7e4658495d33c
source Publicly Available Content Database; Taylor & Francis Open Access Journals; PubMed Central
subjects adipocyte development
Adipocytes
Analysis
Angiogenesis
Body mass index
Breast cancer
Cancer metastasis
Cancer patients
Cancer research
chemerin expression
Development and progression
Disease
Esophagus
Estrogens
Family medical history
Gene expression
Genetic aspects
Health aspects
Immunohistochemistry
Inflammation
Insulin
Insulin-like growth factors
Internal medicine
Ligands
Lung cancer
Medical research
Medicine
Melanoma
Metabolic syndrome
Obesity
Original Research
Phenols (Class of compounds)
Progesterone
Prognosis
Sex hormones
Tumor necrosis factor-TNF
Tumors
Women's health
title Expression of chemerin correlates with a poor prognosis in female breast cancer patients
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T06%3A27%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Expression%20of%20chemerin%20correlates%20with%20a%20poor%20prognosis%20in%20female%20breast%20cancer%20patients&rft.jtitle=Breast%20cancer%20targets%20and%20therapy&rft.au=El-Sagheer,%20Ghada&rft.date=2018-01-01&rft.volume=10&rft.spage=169&rft.epage=176&rft.pages=169-176&rft.issn=1179-1314&rft.eissn=1179-1314&rft_id=info:doi/10.2147/BCTT.S178181&rft_dat=%3Cgale_doaj_%3EA574315023%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c619t-6618c2cbc31e6af75d6de9861acae49e069263e6893546274e8bc192b177865d3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2224000868&rft_id=info:pmid/30498371&rft_galeid=A574315023&rfr_iscdi=true