Direct Comparison of Metastasis-Related miRNAs Expression Levels in Circulating Tumor Cells, Corresponding Plasma, and Primary Tumors of Breast Cancer Patients
Circulating tumor cells (CTCs) and microRNAs (miRNAs) are important in liquid biopsies in which peripheral blood is used to characterize the evolution of solid tumors. We evaluated the expression levels of miR-21, miR-146a, miR-200c, and miR-210 in CTCs of breast cancer patients with verified metast...
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Veröffentlicht in: | Clinical chemistry (Baltimore, Md.) Md.), 2016-07, Vol.62 (7), p.1002-1011 |
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creator | Markou, Athina Zavridou, Martha Sourvinou, Ioanna Yousef, George Kounelis, Sofia Malamos, Nikos Georgoulias, Vasilis Lianidou, Evi |
description | Circulating tumor cells (CTCs) and microRNAs (miRNAs) are important in liquid biopsies in which peripheral blood is used to characterize the evolution of solid tumors. We evaluated the expression levels of miR-21, miR-146a, miR-200c, and miR-210 in CTCs of breast cancer patients with verified metastasis and compared their expression levels in corresponding plasma and primary tumors.
Expression levels of the miRNAs were quantified by quantitative reverse transcription PCR (RT-qPCR) in (a) 89 primary breast tumors and 30 noncancerous breast tissues and (b) CTCs and corresponding plasma of 55 patients with metastatic breast cancer and 20 healthy donors. For 30 of these patients, CTCs, corresponding plasma, and primary tumor tissues were available.
In formalin-fixed, paraffin-embedded tissues, these miRNAs were differentially expressed between primary breast tumors and noncancerous breast tissues. miR-21 (P < 0.001) and miR-146a (P = 0.001) were overexpressed, whereas miR-200c (P = 0.004) and miR-210 (P = 0.002) were underexpressed. In multivariate analysis, miR-146a overexpression was significantly [hazard ratio 2.969 (1.231-7.157), P = 0.015] associated with progression-free survival. In peripheral blood, all miRNAs studied were overexpressed in both CTC and corresponding plasma. There was a significant association between miR-21 expression levels in CTCs and plasma for 36 of 55 samples (P = 0.008). In plasma, ROC curve analysis revealed that miR-21, miR-146a, and miR-210 could discriminate patients from healthy individuals.
Metastasis-related miRNAs are overexpressed in CTCs and corresponding plasma; miR-21 expression levels highly correlate in CTCs and plasma; and miR-21, miR-146a, and miR-210 are valuable plasma biomarkers for discriminating patients from healthy individuals. |
doi_str_mv | 10.1373/clinchem.2015.253716 |
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Expression levels of the miRNAs were quantified by quantitative reverse transcription PCR (RT-qPCR) in (a) 89 primary breast tumors and 30 noncancerous breast tissues and (b) CTCs and corresponding plasma of 55 patients with metastatic breast cancer and 20 healthy donors. For 30 of these patients, CTCs, corresponding plasma, and primary tumor tissues were available.
In formalin-fixed, paraffin-embedded tissues, these miRNAs were differentially expressed between primary breast tumors and noncancerous breast tissues. miR-21 (P < 0.001) and miR-146a (P = 0.001) were overexpressed, whereas miR-200c (P = 0.004) and miR-210 (P = 0.002) were underexpressed. In multivariate analysis, miR-146a overexpression was significantly [hazard ratio 2.969 (1.231-7.157), P = 0.015] associated with progression-free survival. In peripheral blood, all miRNAs studied were overexpressed in both CTC and corresponding plasma. There was a significant association between miR-21 expression levels in CTCs and plasma for 36 of 55 samples (P = 0.008). In plasma, ROC curve analysis revealed that miR-21, miR-146a, and miR-210 could discriminate patients from healthy individuals.
Metastasis-related miRNAs are overexpressed in CTCs and corresponding plasma; miR-21 expression levels highly correlate in CTCs and plasma; and miR-21, miR-146a, and miR-210 are valuable plasma biomarkers for discriminating patients from healthy individuals.</description><identifier>ISSN: 0009-9147</identifier><identifier>EISSN: 1530-8561</identifier><identifier>DOI: 10.1373/clinchem.2015.253716</identifier><identifier>PMID: 27197674</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Biomarkers ; Breast cancer ; Breast Neoplasms - blood ; Breast Neoplasms - genetics ; Breast Neoplasms - pathology ; Conflicts of interest ; Female ; Funding ; Gene expression ; Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; Humans ; Metastasis ; MicroRNAs - blood ; MicroRNAs - genetics ; Multivariate analysis ; Neoplastic Cells, Circulating - metabolism ; Neoplastic Cells, Circulating - pathology ; Plasma ; Prostate cancer ; Reverse Transcriptase Polymerase Chain Reaction ; Tumors</subject><ispartof>Clinical chemistry (Baltimore, Md.), 2016-07, Vol.62 (7), p.1002-1011</ispartof><rights>2016 American Association for Clinical Chemistry.</rights><rights>Copyright American Association for Clinical Chemistry Jul 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-1fe827f7305bb55b3129d6dfaaa688e6052360248294bfc8ea27f351b68744523</citedby><cites>FETCH-LOGICAL-c381t-1fe827f7305bb55b3129d6dfaaa688e6052360248294bfc8ea27f351b68744523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27197674$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Markou, Athina</creatorcontrib><creatorcontrib>Zavridou, Martha</creatorcontrib><creatorcontrib>Sourvinou, Ioanna</creatorcontrib><creatorcontrib>Yousef, George</creatorcontrib><creatorcontrib>Kounelis, Sofia</creatorcontrib><creatorcontrib>Malamos, Nikos</creatorcontrib><creatorcontrib>Georgoulias, Vasilis</creatorcontrib><creatorcontrib>Lianidou, Evi</creatorcontrib><title>Direct Comparison of Metastasis-Related miRNAs Expression Levels in Circulating Tumor Cells, Corresponding Plasma, and Primary Tumors of Breast Cancer Patients</title><title>Clinical chemistry (Baltimore, Md.)</title><addtitle>Clin Chem</addtitle><description>Circulating tumor cells (CTCs) and microRNAs (miRNAs) are important in liquid biopsies in which peripheral blood is used to characterize the evolution of solid tumors. We evaluated the expression levels of miR-21, miR-146a, miR-200c, and miR-210 in CTCs of breast cancer patients with verified metastasis and compared their expression levels in corresponding plasma and primary tumors.
Expression levels of the miRNAs were quantified by quantitative reverse transcription PCR (RT-qPCR) in (a) 89 primary breast tumors and 30 noncancerous breast tissues and (b) CTCs and corresponding plasma of 55 patients with metastatic breast cancer and 20 healthy donors. For 30 of these patients, CTCs, corresponding plasma, and primary tumor tissues were available.
In formalin-fixed, paraffin-embedded tissues, these miRNAs were differentially expressed between primary breast tumors and noncancerous breast tissues. miR-21 (P < 0.001) and miR-146a (P = 0.001) were overexpressed, whereas miR-200c (P = 0.004) and miR-210 (P = 0.002) were underexpressed. In multivariate analysis, miR-146a overexpression was significantly [hazard ratio 2.969 (1.231-7.157), P = 0.015] associated with progression-free survival. In peripheral blood, all miRNAs studied were overexpressed in both CTC and corresponding plasma. There was a significant association between miR-21 expression levels in CTCs and plasma for 36 of 55 samples (P = 0.008). In plasma, ROC curve analysis revealed that miR-21, miR-146a, and miR-210 could discriminate patients from healthy individuals.
Metastasis-related miRNAs are overexpressed in CTCs and corresponding plasma; miR-21 expression levels highly correlate in CTCs and plasma; and miR-21, miR-146a, and miR-210 are valuable plasma biomarkers for discriminating patients from healthy individuals.</description><subject>Biomarkers</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - blood</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - pathology</subject><subject>Conflicts of interest</subject><subject>Female</subject><subject>Funding</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Metastasis</subject><subject>MicroRNAs - blood</subject><subject>MicroRNAs - genetics</subject><subject>Multivariate analysis</subject><subject>Neoplastic Cells, Circulating - metabolism</subject><subject>Neoplastic Cells, Circulating - pathology</subject><subject>Plasma</subject><subject>Prostate cancer</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Tumors</subject><issn>0009-9147</issn><issn>1530-8561</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkc9u1DAQxi0EotuFN0DIEhcOzWLHju0cS2gBaYFVVc6Rk0zAVWIHT4LgaXhVHKXlgGRpZM1vvvnzEfKCswMXWrxpB-fb7zAecsaLQ14IzdUjsuOFYJkpFH9MdoyxMiu51GfkHPEufaU26ik5yzUvtdJyR_68cxHamVZhnGx0GDwNPf0Es8X0HGY3MNgZOjq6m8-XSK9-TREQXeKO8BMGpM7TysV2SZjz3-jtMoZIKxgGvEiqMdFT8N2aOg0WR3tBre_oKbrRxt8bjmvPtxFST1pZ30Kkp6QGfsZn5ElvB4Tn93FPvl5f3VYfsuOX9x-ry2PWCsPnjPdgct1rwYqmKYpG8LzsVNdba5UxoFiRC8VyafJSNn1rwCZaFLxRRkuZknvyetOdYvixAM716LBNW1gPYcGaG8Z0Ekjn3ZNX_6F3YYk-TbdSuSwllypRcqPaGBAj9PW0rVxzVq8G1g8G1quB9WZgKnt5L740I3T_ih4cE38BX_OZww</recordid><startdate>201607</startdate><enddate>201607</enddate><creator>Markou, Athina</creator><creator>Zavridou, Martha</creator><creator>Sourvinou, Ioanna</creator><creator>Yousef, George</creator><creator>Kounelis, Sofia</creator><creator>Malamos, Nikos</creator><creator>Georgoulias, Vasilis</creator><creator>Lianidou, Evi</creator><general>Oxford University Press</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>4U-</scope><scope>7QO</scope><scope>7RV</scope><scope>7TM</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>201607</creationdate><title>Direct Comparison of Metastasis-Related miRNAs Expression Levels in Circulating Tumor Cells, Corresponding Plasma, and Primary Tumors of Breast Cancer Patients</title><author>Markou, Athina ; Zavridou, Martha ; Sourvinou, Ioanna ; Yousef, George ; Kounelis, Sofia ; Malamos, Nikos ; Georgoulias, Vasilis ; Lianidou, Evi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-1fe827f7305bb55b3129d6dfaaa688e6052360248294bfc8ea27f351b68744523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Biomarkers</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - 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Academic</collection><jtitle>Clinical chemistry (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Markou, Athina</au><au>Zavridou, Martha</au><au>Sourvinou, Ioanna</au><au>Yousef, George</au><au>Kounelis, Sofia</au><au>Malamos, Nikos</au><au>Georgoulias, Vasilis</au><au>Lianidou, Evi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Direct Comparison of Metastasis-Related miRNAs Expression Levels in Circulating Tumor Cells, Corresponding Plasma, and Primary Tumors of Breast Cancer Patients</atitle><jtitle>Clinical chemistry (Baltimore, Md.)</jtitle><addtitle>Clin Chem</addtitle><date>2016-07</date><risdate>2016</risdate><volume>62</volume><issue>7</issue><spage>1002</spage><epage>1011</epage><pages>1002-1011</pages><issn>0009-9147</issn><eissn>1530-8561</eissn><abstract>Circulating tumor cells (CTCs) and microRNAs (miRNAs) are important in liquid biopsies in which peripheral blood is used to characterize the evolution of solid tumors. We evaluated the expression levels of miR-21, miR-146a, miR-200c, and miR-210 in CTCs of breast cancer patients with verified metastasis and compared their expression levels in corresponding plasma and primary tumors.
Expression levels of the miRNAs were quantified by quantitative reverse transcription PCR (RT-qPCR) in (a) 89 primary breast tumors and 30 noncancerous breast tissues and (b) CTCs and corresponding plasma of 55 patients with metastatic breast cancer and 20 healthy donors. For 30 of these patients, CTCs, corresponding plasma, and primary tumor tissues were available.
In formalin-fixed, paraffin-embedded tissues, these miRNAs were differentially expressed between primary breast tumors and noncancerous breast tissues. miR-21 (P < 0.001) and miR-146a (P = 0.001) were overexpressed, whereas miR-200c (P = 0.004) and miR-210 (P = 0.002) were underexpressed. In multivariate analysis, miR-146a overexpression was significantly [hazard ratio 2.969 (1.231-7.157), P = 0.015] associated with progression-free survival. In peripheral blood, all miRNAs studied were overexpressed in both CTC and corresponding plasma. There was a significant association between miR-21 expression levels in CTCs and plasma for 36 of 55 samples (P = 0.008). In plasma, ROC curve analysis revealed that miR-21, miR-146a, and miR-210 could discriminate patients from healthy individuals.
Metastasis-related miRNAs are overexpressed in CTCs and corresponding plasma; miR-21 expression levels highly correlate in CTCs and plasma; and miR-21, miR-146a, and miR-210 are valuable plasma biomarkers for discriminating patients from healthy individuals.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>27197674</pmid><doi>10.1373/clinchem.2015.253716</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biomarkers Breast cancer Breast Neoplasms - blood Breast Neoplasms - genetics Breast Neoplasms - pathology Conflicts of interest Female Funding Gene expression Gene Expression Profiling Gene Expression Regulation, Neoplastic Humans Metastasis MicroRNAs - blood MicroRNAs - genetics Multivariate analysis Neoplastic Cells, Circulating - metabolism Neoplastic Cells, Circulating - pathology Plasma Prostate cancer Reverse Transcriptase Polymerase Chain Reaction Tumors |
title | Direct Comparison of Metastasis-Related miRNAs Expression Levels in Circulating Tumor Cells, Corresponding Plasma, and Primary Tumors of Breast Cancer Patients |
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