Loading…

Association between Lymph Node Status and Expression Levels of Androgen Receptor, miR-185, miR-205, and miR-21 in Breast Cancer Subtypes

Breast cancer is the most commonly diagnosed cancer among women. Difficulties in treating breast cancer are associated with the occurrence of metastases at early stages of disease, leading to its further progression. Recent studies have shown that changes in androgen receptor (AR) and microRNAs’ exp...

Full description

Saved in:
Bibliographic Details
Published in:International journal of breast cancer 2020, Vol.2020 (2020), p.1-7
Main Authors: Sidorov, Sergey V., Alekseenok, Efim Y., Yakovleva, Alisa K., Kononchuk, Vladislav V., Kalinina, Tatiana S., Gulyaeva, Lyudmila F.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
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-c635t-1f151d94be4dc871910ea43ea44b472e971d885aca90c8f8f2b4d4bf53333cff3
cites cdi_FETCH-LOGICAL-c635t-1f151d94be4dc871910ea43ea44b472e971d885aca90c8f8f2b4d4bf53333cff3
container_end_page 7
container_issue 2020
container_start_page 1
container_title International journal of breast cancer
container_volume 2020
creator Sidorov, Sergey V.
Alekseenok, Efim Y.
Yakovleva, Alisa K.
Kononchuk, Vladislav V.
Kalinina, Tatiana S.
Gulyaeva, Lyudmila F.
description Breast cancer is the most commonly diagnosed cancer among women. Difficulties in treating breast cancer are associated with the occurrence of metastases at early stages of disease, leading to its further progression. Recent studies have shown that changes in androgen receptor (AR) and microRNAs’ expressions are associated with mammary gland carcinogenesis, in particular, with the formation of metastases. Thus, to identify novel metastatic markers, we evaluated the expression levels of AR; miR-185 and miR-205, both of which have been confirmed to target AR; and miR-21, transcription of which is regulated by AR, in breast cancer samples (n=89). Here, we show that the molecular subtypes of breast cancer differ in the expression profiles of AR and AR-associated microRNAs. In addition, the expression of AR and these microRNAs may depend on the expression of PR, ER, and HER2 receptors. Our results show that the possibility of using AR and microRNAs as markers depends on the tumor subtype: a decrease in AR expression may be the marker for the presence of lymph node metastases in patients with HER2-positive subtypes of breast cancer, and disturbance of miR-205, miR-185, and miR-21 expressions may be the marker in patients with a luminal B HER2-positive subtype. Cases with metastases in this type of breast cancer are characterized by a higher level of miR-205 and a lower level of miR-185 and miR-21 in tumor tissues compared to nonmetastatic cases. A decrease in the miR-185 level is also associated with lymph node metastasis in luminal B HER2-negative breast cancer. Thus, the expression levels of AR, miR-185, miR-205, and miR-21 can serve as markers to predict cancer spread to the lymph node in luminal B- and HER2-positive subtypes of breast cancer.
doi_str_mv 10.1155/2020/3259393
format article
fullrecord <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_e16457b2819348cca224b78065cafd31</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A627507674</galeid><doaj_id>oai_doaj_org_article_e16457b2819348cca224b78065cafd31</doaj_id><sourcerecordid>A627507674</sourcerecordid><originalsourceid>FETCH-LOGICAL-c635t-1f151d94be4dc871910ea43ea44b472e971d885aca90c8f8f2b4d4bf53333cff3</originalsourceid><addsrcrecordid>eNqNkl1rFDEUhgdRbKm981oCggh223zOx42wLlULi0Kr1yGTOdnNMpOsyUzr_gN_tpnuuu2KFyaEOck8501y8mbZS4LPCRHigmKKLxgVFavYk-yY4gpPGCmrp_u4wEfZaYwrnJogjOXF8-yIUVaM4XH2axqj11b11jtUQ38H4NB8062X6ItvAN30qh8iUq5Blz_XAWIcwTncQhuRN2jqmuAXKecaNKx7H85QZ68npBTbgOIUjNn3E4KsQx8CqNijmXIaAroZ6n6zhvgie2ZUG-F09z3Jvn-8_Db7PJl__XQ1m84nOmeinxBDBGkqXgNvdFmQimBQnKXBa15QqArSlKVQWlVYl6Y0tOYNr41gqWlj2El2tdVtvFrJdbCdChvplZX3Cz4spAq91S1IIDkXRU1LUjFeaq0o5XVR4lxoZRpGktb7rdZ6qDtoNLg-qPZA9PCPs0u58LcynVvkfBR4uxMI_scAsZedjRraVjnwQ5SUVVV6qvR0CX39F7ryQ3CpVCNV8DInJX-gFipdwDrj0756FJXTnBYCF3kxUuf_oFJvoLPaOzA2rR8kvHmUsATV9svo22F0TTwEz7agDj7GAGZfDILl6Fg5OlbuHJvwV48LuIf_-DMB77bA0rpG3dn_lIPEgFEPNMkrQjj7DZkX-Co</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2397486184</pqid></control><display><type>article</type><title>Association between Lymph Node Status and Expression Levels of Androgen Receptor, miR-185, miR-205, and miR-21 in Breast Cancer Subtypes</title><source>Publicly Available Content (ProQuest)</source><source>Wiley Open Access</source><source>PubMed Central</source><creator>Sidorov, Sergey V. ; Alekseenok, Efim Y. ; Yakovleva, Alisa K. ; Kononchuk, Vladislav V. ; Kalinina, Tatiana S. ; Gulyaeva, Lyudmila F.</creator><contributor>McIlroy, Marie ; Marie McIlroy</contributor><creatorcontrib>Sidorov, Sergey V. ; Alekseenok, Efim Y. ; Yakovleva, Alisa K. ; Kononchuk, Vladislav V. ; Kalinina, Tatiana S. ; Gulyaeva, Lyudmila F. ; McIlroy, Marie ; Marie McIlroy</creatorcontrib><description>Breast cancer is the most commonly diagnosed cancer among women. Difficulties in treating breast cancer are associated with the occurrence of metastases at early stages of disease, leading to its further progression. Recent studies have shown that changes in androgen receptor (AR) and microRNAs’ expressions are associated with mammary gland carcinogenesis, in particular, with the formation of metastases. Thus, to identify novel metastatic markers, we evaluated the expression levels of AR; miR-185 and miR-205, both of which have been confirmed to target AR; and miR-21, transcription of which is regulated by AR, in breast cancer samples (n=89). Here, we show that the molecular subtypes of breast cancer differ in the expression profiles of AR and AR-associated microRNAs. In addition, the expression of AR and these microRNAs may depend on the expression of PR, ER, and HER2 receptors. Our results show that the possibility of using AR and microRNAs as markers depends on the tumor subtype: a decrease in AR expression may be the marker for the presence of lymph node metastases in patients with HER2-positive subtypes of breast cancer, and disturbance of miR-205, miR-185, and miR-21 expressions may be the marker in patients with a luminal B HER2-positive subtype. Cases with metastases in this type of breast cancer are characterized by a higher level of miR-205 and a lower level of miR-185 and miR-21 in tumor tissues compared to nonmetastatic cases. A decrease in the miR-185 level is also associated with lymph node metastasis in luminal B HER2-negative breast cancer. Thus, the expression levels of AR, miR-185, miR-205, and miR-21 can serve as markers to predict cancer spread to the lymph node in luminal B- and HER2-positive subtypes of breast cancer.</description><identifier>ISSN: 2090-3170</identifier><identifier>ISSN: 2090-3189</identifier><identifier>EISSN: 2090-3189</identifier><identifier>DOI: 10.1155/2020/3259393</identifier><identifier>PMID: 32373367</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Androgen receptors ; Androgens ; Breast cancer ; Cancer ; Carcinogenesis ; Care and treatment ; Development and progression ; ErbB-2 protein ; Gene expression ; Laboratories ; Lymph nodes ; Mammary gland ; Metastases ; Metastasis ; MicroRNA ; MicroRNAs ; miRNA ; Transcription</subject><ispartof>International journal of breast cancer, 2020, Vol.2020 (2020), p.1-7</ispartof><rights>Copyright © 2020 Tatiana S. Kalinina et al.</rights><rights>COPYRIGHT 2020 John Wiley &amp; Sons, Inc.</rights><rights>Copyright © 2020 Tatiana S. Kalinina et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2020 Tatiana S. Kalinina et al. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c635t-1f151d94be4dc871910ea43ea44b472e971d885aca90c8f8f2b4d4bf53333cff3</citedby><cites>FETCH-LOGICAL-c635t-1f151d94be4dc871910ea43ea44b472e971d885aca90c8f8f2b4d4bf53333cff3</cites><orcidid>0000-0002-2698-0866</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2397486184/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2397486184?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,4024,25753,27923,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32373367$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>McIlroy, Marie</contributor><contributor>Marie McIlroy</contributor><creatorcontrib>Sidorov, Sergey V.</creatorcontrib><creatorcontrib>Alekseenok, Efim Y.</creatorcontrib><creatorcontrib>Yakovleva, Alisa K.</creatorcontrib><creatorcontrib>Kononchuk, Vladislav V.</creatorcontrib><creatorcontrib>Kalinina, Tatiana S.</creatorcontrib><creatorcontrib>Gulyaeva, Lyudmila F.</creatorcontrib><title>Association between Lymph Node Status and Expression Levels of Androgen Receptor, miR-185, miR-205, and miR-21 in Breast Cancer Subtypes</title><title>International journal of breast cancer</title><addtitle>Int J Breast Cancer</addtitle><description>Breast cancer is the most commonly diagnosed cancer among women. Difficulties in treating breast cancer are associated with the occurrence of metastases at early stages of disease, leading to its further progression. Recent studies have shown that changes in androgen receptor (AR) and microRNAs’ expressions are associated with mammary gland carcinogenesis, in particular, with the formation of metastases. Thus, to identify novel metastatic markers, we evaluated the expression levels of AR; miR-185 and miR-205, both of which have been confirmed to target AR; and miR-21, transcription of which is regulated by AR, in breast cancer samples (n=89). Here, we show that the molecular subtypes of breast cancer differ in the expression profiles of AR and AR-associated microRNAs. In addition, the expression of AR and these microRNAs may depend on the expression of PR, ER, and HER2 receptors. Our results show that the possibility of using AR and microRNAs as markers depends on the tumor subtype: a decrease in AR expression may be the marker for the presence of lymph node metastases in patients with HER2-positive subtypes of breast cancer, and disturbance of miR-205, miR-185, and miR-21 expressions may be the marker in patients with a luminal B HER2-positive subtype. Cases with metastases in this type of breast cancer are characterized by a higher level of miR-205 and a lower level of miR-185 and miR-21 in tumor tissues compared to nonmetastatic cases. A decrease in the miR-185 level is also associated with lymph node metastasis in luminal B HER2-negative breast cancer. Thus, the expression levels of AR, miR-185, miR-205, and miR-21 can serve as markers to predict cancer spread to the lymph node in luminal B- and HER2-positive subtypes of breast cancer.</description><subject>Androgen receptors</subject><subject>Androgens</subject><subject>Breast cancer</subject><subject>Cancer</subject><subject>Carcinogenesis</subject><subject>Care and treatment</subject><subject>Development and progression</subject><subject>ErbB-2 protein</subject><subject>Gene expression</subject><subject>Laboratories</subject><subject>Lymph nodes</subject><subject>Mammary gland</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>MicroRNA</subject><subject>MicroRNAs</subject><subject>miRNA</subject><subject>Transcription</subject><issn>2090-3170</issn><issn>2090-3189</issn><issn>2090-3189</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNkl1rFDEUhgdRbKm981oCggh223zOx42wLlULi0Kr1yGTOdnNMpOsyUzr_gN_tpnuuu2KFyaEOck8501y8mbZS4LPCRHigmKKLxgVFavYk-yY4gpPGCmrp_u4wEfZaYwrnJogjOXF8-yIUVaM4XH2axqj11b11jtUQ38H4NB8062X6ItvAN30qh8iUq5Blz_XAWIcwTncQhuRN2jqmuAXKecaNKx7H85QZ68npBTbgOIUjNn3E4KsQx8CqNijmXIaAroZ6n6zhvgie2ZUG-F09z3Jvn-8_Db7PJl__XQ1m84nOmeinxBDBGkqXgNvdFmQimBQnKXBa15QqArSlKVQWlVYl6Y0tOYNr41gqWlj2El2tdVtvFrJdbCdChvplZX3Cz4spAq91S1IIDkXRU1LUjFeaq0o5XVR4lxoZRpGktb7rdZ6qDtoNLg-qPZA9PCPs0u58LcynVvkfBR4uxMI_scAsZedjRraVjnwQ5SUVVV6qvR0CX39F7ryQ3CpVCNV8DInJX-gFipdwDrj0756FJXTnBYCF3kxUuf_oFJvoLPaOzA2rR8kvHmUsATV9svo22F0TTwEz7agDj7GAGZfDILl6Fg5OlbuHJvwV48LuIf_-DMB77bA0rpG3dn_lIPEgFEPNMkrQjj7DZkX-Co</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Sidorov, Sergey V.</creator><creator>Alekseenok, Efim Y.</creator><creator>Yakovleva, Alisa K.</creator><creator>Kononchuk, Vladislav V.</creator><creator>Kalinina, Tatiana S.</creator><creator>Gulyaeva, Lyudmila F.</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</general><general>John Wiley &amp; Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><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>PADUT</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/0000-0002-2698-0866</orcidid></search><sort><creationdate>2020</creationdate><title>Association between Lymph Node Status and Expression Levels of Androgen Receptor, miR-185, miR-205, and miR-21 in Breast Cancer Subtypes</title><author>Sidorov, Sergey V. ; Alekseenok, Efim Y. ; Yakovleva, Alisa K. ; Kononchuk, Vladislav V. ; Kalinina, Tatiana S. ; Gulyaeva, Lyudmila F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c635t-1f151d94be4dc871910ea43ea44b472e971d885aca90c8f8f2b4d4bf53333cff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Androgen receptors</topic><topic>Androgens</topic><topic>Breast cancer</topic><topic>Cancer</topic><topic>Carcinogenesis</topic><topic>Care and treatment</topic><topic>Development and progression</topic><topic>ErbB-2 protein</topic><topic>Gene expression</topic><topic>Laboratories</topic><topic>Lymph nodes</topic><topic>Mammary gland</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>MicroRNA</topic><topic>MicroRNAs</topic><topic>miRNA</topic><topic>Transcription</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sidorov, Sergey V.</creatorcontrib><creatorcontrib>Alekseenok, Efim Y.</creatorcontrib><creatorcontrib>Yakovleva, Alisa K.</creatorcontrib><creatorcontrib>Kononchuk, Vladislav V.</creatorcontrib><creatorcontrib>Kalinina, Tatiana S.</creatorcontrib><creatorcontrib>Gulyaeva, Lyudmila F.</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><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 Korea</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>Research Library China</collection><collection>Publicly Available Content (ProQuest)</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>International journal of breast cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sidorov, Sergey V.</au><au>Alekseenok, Efim Y.</au><au>Yakovleva, Alisa K.</au><au>Kononchuk, Vladislav V.</au><au>Kalinina, Tatiana S.</au><au>Gulyaeva, Lyudmila F.</au><au>McIlroy, Marie</au><au>Marie McIlroy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between Lymph Node Status and Expression Levels of Androgen Receptor, miR-185, miR-205, and miR-21 in Breast Cancer Subtypes</atitle><jtitle>International journal of breast cancer</jtitle><addtitle>Int J Breast Cancer</addtitle><date>2020</date><risdate>2020</risdate><volume>2020</volume><issue>2020</issue><spage>1</spage><epage>7</epage><pages>1-7</pages><issn>2090-3170</issn><issn>2090-3189</issn><eissn>2090-3189</eissn><abstract>Breast cancer is the most commonly diagnosed cancer among women. Difficulties in treating breast cancer are associated with the occurrence of metastases at early stages of disease, leading to its further progression. Recent studies have shown that changes in androgen receptor (AR) and microRNAs’ expressions are associated with mammary gland carcinogenesis, in particular, with the formation of metastases. Thus, to identify novel metastatic markers, we evaluated the expression levels of AR; miR-185 and miR-205, both of which have been confirmed to target AR; and miR-21, transcription of which is regulated by AR, in breast cancer samples (n=89). Here, we show that the molecular subtypes of breast cancer differ in the expression profiles of AR and AR-associated microRNAs. In addition, the expression of AR and these microRNAs may depend on the expression of PR, ER, and HER2 receptors. Our results show that the possibility of using AR and microRNAs as markers depends on the tumor subtype: a decrease in AR expression may be the marker for the presence of lymph node metastases in patients with HER2-positive subtypes of breast cancer, and disturbance of miR-205, miR-185, and miR-21 expressions may be the marker in patients with a luminal B HER2-positive subtype. Cases with metastases in this type of breast cancer are characterized by a higher level of miR-205 and a lower level of miR-185 and miR-21 in tumor tissues compared to nonmetastatic cases. A decrease in the miR-185 level is also associated with lymph node metastasis in luminal B HER2-negative breast cancer. Thus, the expression levels of AR, miR-185, miR-205, and miR-21 can serve as markers to predict cancer spread to the lymph node in luminal B- and HER2-positive subtypes of breast cancer.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>32373367</pmid><doi>10.1155/2020/3259393</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-2698-0866</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2090-3170
ispartof International journal of breast cancer, 2020, Vol.2020 (2020), p.1-7
issn 2090-3170
2090-3189
2090-3189
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_e16457b2819348cca224b78065cafd31
source Publicly Available Content (ProQuest); Wiley Open Access; PubMed Central
subjects Androgen receptors
Androgens
Breast cancer
Cancer
Carcinogenesis
Care and treatment
Development and progression
ErbB-2 protein
Gene expression
Laboratories
Lymph nodes
Mammary gland
Metastases
Metastasis
MicroRNA
MicroRNAs
miRNA
Transcription
title Association between Lymph Node Status and Expression Levels of Androgen Receptor, miR-185, miR-205, and miR-21 in Breast Cancer Subtypes
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T17%3A06%3A27IST&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=Association%20between%20Lymph%20Node%20Status%20and%20Expression%20Levels%20of%20Androgen%20Receptor,%20miR-185,%20miR-205,%20and%20miR-21%20in%20Breast%20Cancer%20Subtypes&rft.jtitle=International%20journal%20of%20breast%20cancer&rft.au=Sidorov,%20Sergey%20V.&rft.date=2020&rft.volume=2020&rft.issue=2020&rft.spage=1&rft.epage=7&rft.pages=1-7&rft.issn=2090-3170&rft.eissn=2090-3189&rft_id=info:doi/10.1155/2020/3259393&rft_dat=%3Cgale_doaj_%3EA627507674%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c635t-1f151d94be4dc871910ea43ea44b472e971d885aca90c8f8f2b4d4bf53333cff3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2397486184&rft_id=info:pmid/32373367&rft_galeid=A627507674&rfr_iscdi=true