miRNA profiling reveals a potential role of milk stasis in breast carcinogenesis
The tumor microenvironment plays an important role in breast carcinogenesis. Milk acts as an important microenvironment of breast cancer, but its role in breast carcinogenesis is largely unknown. Milk stasis may exist in the breast for a number of years after breastfeeding. In the present study, we...
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Veröffentlicht in: | International journal of molecular medicine 2014-05, Vol.33 (5), p.1243-1249 |
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description | The tumor microenvironment plays an important role in breast carcinogenesis. Milk acts as an important microenvironment of breast cancer, but its role in breast carcinogenesis is largely unknown. Milk stasis may exist in the breast for a number of years after breastfeeding. In the present study, we reported the first microRNA (miRNA) profiling of milk from patients with milk stasis. We identified 266 known miRNAs and 271 novel miRNAs in 10 milk stasis only samples, 271 known miRNAs and 140 novel miRNAs in 10 milk stasis plus breast neoplasm samples by deep sequencing. miRNA profiles were different between the two groups. Furthermore, nine tumor suppressor miRNAs such as miR-29a, miR-146 and miR-223 were significantly downregulated, while seven oncogenic miRNAs such as miR-451, miR-486, miR-107, miR-92 and miR-10 were significantly upregulated in the milk of milk stasis plus neoplasm patients. Three of the identified miRNAs (miR-140, miR-21 and let-7a) were selected using real-time PCR, confirming that these miRNAs were highly expressed. The results also showed that the three miRNAs detected were more abundant in the milk than in the blood. In summary, the data suggested that miRNAs in milk from milk stasis patients may contribute to breast carcinogenesis and that they are more sensitive biomarkers for breast cancer than miRNAs in the blood. |
doi_str_mv | 10.3892/ijmm.2014.1677 |
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Milk acts as an important microenvironment of breast cancer, but its role in breast carcinogenesis is largely unknown. Milk stasis may exist in the breast for a number of years after breastfeeding. In the present study, we reported the first microRNA (miRNA) profiling of milk from patients with milk stasis. We identified 266 known miRNAs and 271 novel miRNAs in 10 milk stasis only samples, 271 known miRNAs and 140 novel miRNAs in 10 milk stasis plus breast neoplasm samples by deep sequencing. miRNA profiles were different between the two groups. Furthermore, nine tumor suppressor miRNAs such as miR-29a, miR-146 and miR-223 were significantly downregulated, while seven oncogenic miRNAs such as miR-451, miR-486, miR-107, miR-92 and miR-10 were significantly upregulated in the milk of milk stasis plus neoplasm patients. Three of the identified miRNAs (miR-140, miR-21 and let-7a) were selected using real-time PCR, confirming that these miRNAs were highly expressed. The results also showed that the three miRNAs detected were more abundant in the milk than in the blood. In summary, the data suggested that miRNAs in milk from milk stasis patients may contribute to breast carcinogenesis and that they are more sensitive biomarkers for breast cancer than miRNAs in the blood.</description><identifier>ISSN: 1107-3756</identifier><identifier>EISSN: 1791-244X</identifier><identifier>DOI: 10.3892/ijmm.2014.1677</identifier><identifier>PMID: 24584717</identifier><language>eng</language><publisher>Greece: D.A. Spandidos</publisher><subject>Adult ; biomarker ; Biomarkers ; Breast cancer ; Breast Diseases - complications ; Breast Diseases - metabolism ; Breast milk ; Breast Neoplasms - genetics ; Breastfeeding & lactation ; Development and progression ; Female ; Gene expression ; Gene Expression Profiling - methods ; Gene Expression Regulation, Neoplastic - genetics ; Gene Expression Regulation, Neoplastic - physiology ; Genetic aspects ; Health aspects ; Health risk assessment ; Humans ; Mammography ; MicroRNA ; MicroRNAs - genetics ; milk stasis ; miRNA ; miRNA profile ; Properties ; Risk factors ; Tumors ; Young Adult</subject><ispartof>International journal of molecular medicine, 2014-05, Vol.33 (5), p.1243-1249</ispartof><rights>Copyright © 2014, Spandidos Publications</rights><rights>COPYRIGHT 2014 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-7d96cea487261adef8f730de3501faaf678454cbc55e8cac9f80ae17beaf968f3</citedby><cites>FETCH-LOGICAL-c463t-7d96cea487261adef8f730de3501faaf678454cbc55e8cac9f80ae17beaf968f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,5556,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24584717$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>GU, YI-QI</creatorcontrib><creatorcontrib>GONG, GU</creatorcontrib><creatorcontrib>XU, ZHE-LI</creatorcontrib><creatorcontrib>WANG, LI-YING</creatorcontrib><creatorcontrib>FANG, MING-LI</creatorcontrib><creatorcontrib>ZHOU, HUI</creatorcontrib><creatorcontrib>XING, HUA</creatorcontrib><creatorcontrib>WANG, KE-REN</creatorcontrib><creatorcontrib>SUN, LIANG</creatorcontrib><title>miRNA profiling reveals a potential role of milk stasis in breast carcinogenesis</title><title>International journal of molecular medicine</title><addtitle>Int J Mol Med</addtitle><description>The tumor microenvironment plays an important role in breast carcinogenesis. Milk acts as an important microenvironment of breast cancer, but its role in breast carcinogenesis is largely unknown. Milk stasis may exist in the breast for a number of years after breastfeeding. In the present study, we reported the first microRNA (miRNA) profiling of milk from patients with milk stasis. We identified 266 known miRNAs and 271 novel miRNAs in 10 milk stasis only samples, 271 known miRNAs and 140 novel miRNAs in 10 milk stasis plus breast neoplasm samples by deep sequencing. miRNA profiles were different between the two groups. Furthermore, nine tumor suppressor miRNAs such as miR-29a, miR-146 and miR-223 were significantly downregulated, while seven oncogenic miRNAs such as miR-451, miR-486, miR-107, miR-92 and miR-10 were significantly upregulated in the milk of milk stasis plus neoplasm patients. Three of the identified miRNAs (miR-140, miR-21 and let-7a) were selected using real-time PCR, confirming that these miRNAs were highly expressed. The results also showed that the three miRNAs detected were more abundant in the milk than in the blood. In summary, the data suggested that miRNAs in milk from milk stasis patients may contribute to breast carcinogenesis and that they are more sensitive biomarkers for breast cancer than miRNAs in the blood.</description><subject>Adult</subject><subject>biomarker</subject><subject>Biomarkers</subject><subject>Breast cancer</subject><subject>Breast Diseases - complications</subject><subject>Breast Diseases - metabolism</subject><subject>Breast milk</subject><subject>Breast Neoplasms - genetics</subject><subject>Breastfeeding & lactation</subject><subject>Development and progression</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Expression Profiling - methods</subject><subject>Gene Expression Regulation, Neoplastic - genetics</subject><subject>Gene Expression Regulation, Neoplastic - physiology</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Health risk assessment</subject><subject>Humans</subject><subject>Mammography</subject><subject>MicroRNA</subject><subject>MicroRNAs - genetics</subject><subject>milk stasis</subject><subject>miRNA</subject><subject>miRNA profile</subject><subject>Properties</subject><subject>Risk factors</subject><subject>Tumors</subject><subject>Young Adult</subject><issn>1107-3756</issn><issn>1791-244X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNptkc9rHCEUxyWkND_aa49ByCWX2eqoo3NcQtIGQltKC73JW-e5uJ3Rjc4W-t_XIT96CR6e4Of7fLwPIR84WwnTtx_DbppWLeNyxTutj8gp1z1vWil_Hdc7Z7oRWnUn5KyUHWOtkr15S05aqYzUXJ-Sb1P4_mVN9zn5MIa4pRn_IIyFAt2nGeMcYKQ5jUiTp1MYf9MyQwmFhkg3GaHM1EF2IaYtRqwP78gbX_P4_qmek5-3Nz-uPzf3Xz_dXa_vGyc7MTd66DuHII1uOw4DeuO1YAMKxbgH8J02Ukm3cUqhceB6bxgg1xsE33fGi3Ny-di3jv5wwDLbXTrkWL-0vBetUFJp_Z_awog2RJ_mDG4Kxdm1FJoxabis1OoVqp4Bp-BSxLobfDXgciolo7f7HCbIfy1ndvFiFy928WIXLzVw8TTtYTPh8II_i6jA1SNQ9hCHMKTywiytGiEaphreSiH-Ad-blgs</recordid><startdate>20140501</startdate><enddate>20140501</enddate><creator>GU, YI-QI</creator><creator>GONG, GU</creator><creator>XU, ZHE-LI</creator><creator>WANG, LI-YING</creator><creator>FANG, MING-LI</creator><creator>ZHOU, HUI</creator><creator>XING, HUA</creator><creator>WANG, KE-REN</creator><creator>SUN, LIANG</creator><general>D.A. Spandidos</general><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20140501</creationdate><title>miRNA profiling reveals a potential role of milk stasis in breast carcinogenesis</title><author>GU, YI-QI ; GONG, GU ; XU, ZHE-LI ; WANG, LI-YING ; FANG, MING-LI ; ZHOU, HUI ; XING, HUA ; WANG, KE-REN ; SUN, LIANG</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-7d96cea487261adef8f730de3501faaf678454cbc55e8cac9f80ae17beaf968f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>biomarker</topic><topic>Biomarkers</topic><topic>Breast cancer</topic><topic>Breast Diseases - complications</topic><topic>Breast Diseases - metabolism</topic><topic>Breast milk</topic><topic>Breast Neoplasms - genetics</topic><topic>Breastfeeding & lactation</topic><topic>Development and progression</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gene Expression Profiling - methods</topic><topic>Gene Expression Regulation, Neoplastic - genetics</topic><topic>Gene Expression Regulation, Neoplastic - physiology</topic><topic>Genetic aspects</topic><topic>Health aspects</topic><topic>Health risk assessment</topic><topic>Humans</topic><topic>Mammography</topic><topic>MicroRNA</topic><topic>MicroRNAs - genetics</topic><topic>milk stasis</topic><topic>miRNA</topic><topic>miRNA profile</topic><topic>Properties</topic><topic>Risk factors</topic><topic>Tumors</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GU, YI-QI</creatorcontrib><creatorcontrib>GONG, GU</creatorcontrib><creatorcontrib>XU, ZHE-LI</creatorcontrib><creatorcontrib>WANG, LI-YING</creatorcontrib><creatorcontrib>FANG, MING-LI</creatorcontrib><creatorcontrib>ZHOU, HUI</creatorcontrib><creatorcontrib>XING, HUA</creatorcontrib><creatorcontrib>WANG, KE-REN</creatorcontrib><creatorcontrib>SUN, LIANG</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical 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><jtitle>International journal of molecular medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>GU, YI-QI</au><au>GONG, GU</au><au>XU, ZHE-LI</au><au>WANG, LI-YING</au><au>FANG, MING-LI</au><au>ZHOU, HUI</au><au>XING, HUA</au><au>WANG, KE-REN</au><au>SUN, LIANG</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>miRNA profiling reveals a potential role of milk stasis in breast carcinogenesis</atitle><jtitle>International journal of molecular medicine</jtitle><addtitle>Int J Mol Med</addtitle><date>2014-05-01</date><risdate>2014</risdate><volume>33</volume><issue>5</issue><spage>1243</spage><epage>1249</epage><pages>1243-1249</pages><issn>1107-3756</issn><eissn>1791-244X</eissn><abstract>The tumor microenvironment plays an important role in breast carcinogenesis. Milk acts as an important microenvironment of breast cancer, but its role in breast carcinogenesis is largely unknown. Milk stasis may exist in the breast for a number of years after breastfeeding. In the present study, we reported the first microRNA (miRNA) profiling of milk from patients with milk stasis. We identified 266 known miRNAs and 271 novel miRNAs in 10 milk stasis only samples, 271 known miRNAs and 140 novel miRNAs in 10 milk stasis plus breast neoplasm samples by deep sequencing. miRNA profiles were different between the two groups. Furthermore, nine tumor suppressor miRNAs such as miR-29a, miR-146 and miR-223 were significantly downregulated, while seven oncogenic miRNAs such as miR-451, miR-486, miR-107, miR-92 and miR-10 were significantly upregulated in the milk of milk stasis plus neoplasm patients. Three of the identified miRNAs (miR-140, miR-21 and let-7a) were selected using real-time PCR, confirming that these miRNAs were highly expressed. The results also showed that the three miRNAs detected were more abundant in the milk than in the blood. In summary, the data suggested that miRNAs in milk from milk stasis patients may contribute to breast carcinogenesis and that they are more sensitive biomarkers for breast cancer than miRNAs in the blood.</abstract><cop>Greece</cop><pub>D.A. Spandidos</pub><pmid>24584717</pmid><doi>10.3892/ijmm.2014.1677</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult biomarker Biomarkers Breast cancer Breast Diseases - complications Breast Diseases - metabolism Breast milk Breast Neoplasms - genetics Breastfeeding & lactation Development and progression Female Gene expression Gene Expression Profiling - methods Gene Expression Regulation, Neoplastic - genetics Gene Expression Regulation, Neoplastic - physiology Genetic aspects Health aspects Health risk assessment Humans Mammography MicroRNA MicroRNAs - genetics milk stasis miRNA miRNA profile Properties Risk factors Tumors Young Adult |
title | miRNA profiling reveals a potential role of milk stasis in breast carcinogenesis |
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