miR-10a-5p and miR-29b-3p as Extracellular Vesicle-Associated Prostate Cancer Detection Markers

Extracellular vesicles (EVs) are shed by many different cell types. Their nucleic acids content offers new opportunities for biomarker research in different solid tumors. The role of EV RNA in prostate cancer (PCa) is still largely unknown. EVs were isolated from different benign and malignant prost...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cancers 2019-12, Vol.12 (1), p.43
Hauptverfasser: Worst, Thomas Stefan, Previti, Christopher, Nitschke, Katja, Diessl, Nicolle, Gross, Julia Christina, Hoffmann, Lena, Frey, Lisa, Thomas, Vanessa, Kahlert, Christoph, Bieback, Karen, Crigna, Adriana Torres, Fricke, Fabia, Porubsky, Stefan, Westhoff, Niklas, Hardenberg, Jost von, Nuhn, Philipp, Erben, Philipp, Michel, Maurice Stephan, Boutros, Michael
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 1
container_start_page 43
container_title Cancers
container_volume 12
creator Worst, Thomas Stefan
Previti, Christopher
Nitschke, Katja
Diessl, Nicolle
Gross, Julia Christina
Hoffmann, Lena
Frey, Lisa
Thomas, Vanessa
Kahlert, Christoph
Bieback, Karen
Crigna, Adriana Torres
Fricke, Fabia
Porubsky, Stefan
Westhoff, Niklas
Hardenberg, Jost von
Nuhn, Philipp
Erben, Philipp
Michel, Maurice Stephan
Boutros, Michael
description Extracellular vesicles (EVs) are shed by many different cell types. Their nucleic acids content offers new opportunities for biomarker research in different solid tumors. The role of EV RNA in prostate cancer (PCa) is still largely unknown. EVs were isolated from different benign and malignant prostate cell lines and blood plasma from patients with PCa ( = 18) and controls with benign prostatic hyperplasia (BPH) ( = 7). Nanoparticle tracking analysis (NTA), Western blot, electron microscopy, and flow cytometry analysis were used for the characterization of EVs. Non-coding RNA expression profiling of PC3 metastatic PCa cells and their EVs was performed by next generation sequencing (NGS). miRNAs differentially expressed in PC3 EVs were validated with qRT-PCR in EVs derived from additional cell lines and patient plasma and from matched tissue samples. 92 miRNAs were enriched and 48 miRNAs were depleted in PC3 EVs compared to PC3 cells, which could be confirmed by qRT-PCR. miR-99b-5p was significantly higher expressed in malignant compared to benign EVs. Furthermore, expression profiling showed miR-10a-5p ( = 0.018) and miR-29b-3p ( = 0.002), but not miR-99b-5p, to be overexpressed in plasma-derived EVs from patients with PCa compared with controls. In the corresponding tissue samples, no significant differences in the miRNA expression could be observed. We thus propose that EV-associated miR-10a-5p and miR-29b-3p could serve as potential new PCa detection markers.
doi_str_mv 10.3390/cancers12010043
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7017198</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2547609872</sourcerecordid><originalsourceid>FETCH-LOGICAL-c421t-7efbf0abc5fbf3d2b62c74c918767d04499e6c4400bf7632b3721933936c78ef3</originalsourceid><addsrcrecordid>eNpdUU1LAzEUDKLYoj17kwUvXmLztcnmIpT6CRVF1GvIZrO6dbupya7ovze1tdTm8t7jTYaZeQAcYXRGqURDoxtjfcAEYYQY3QF9ggSBnEu2u9H3wCCEKYqPUiy42Ac9ijMhBM_6QM2qR4iRhuk80U2RLEYic0jjGJLLr9ZrY-u6q7VPXmyoTG3hKARnKt3aInnwLrSxS8a_WpIL21rTVq5J7rR_j-IOwV6p62AHq3oAnq8un8Y3cHJ_fTseTaBhBLdQ2DIvkc5NGistSM6JEczIqJOLAjEmpeWGMYTyUnBKcioIljEFyo3IbEkPwPmSd97lM1sY20TltZr7aqb9t3K6Uv83TfWmXt2nEggLLLNIcLoi8O6js6GNyYSFdd1Y1wVFYngkJSlGEXqyBZ26zjfRniIpExzJTJCIGi5RJmYUvC3XYjBSi_uprfvFH8ebHtb4v2vRH1nNllw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2547609872</pqid></control><display><type>article</type><title>miR-10a-5p and miR-29b-3p as Extracellular Vesicle-Associated Prostate Cancer Detection Markers</title><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>PubMed Central Open Access</source><creator>Worst, Thomas Stefan ; Previti, Christopher ; Nitschke, Katja ; Diessl, Nicolle ; Gross, Julia Christina ; Hoffmann, Lena ; Frey, Lisa ; Thomas, Vanessa ; Kahlert, Christoph ; Bieback, Karen ; Crigna, Adriana Torres ; Fricke, Fabia ; Porubsky, Stefan ; Westhoff, Niklas ; Hardenberg, Jost von ; Nuhn, Philipp ; Erben, Philipp ; Michel, Maurice Stephan ; Boutros, Michael</creator><creatorcontrib>Worst, Thomas Stefan ; Previti, Christopher ; Nitschke, Katja ; Diessl, Nicolle ; Gross, Julia Christina ; Hoffmann, Lena ; Frey, Lisa ; Thomas, Vanessa ; Kahlert, Christoph ; Bieback, Karen ; Crigna, Adriana Torres ; Fricke, Fabia ; Porubsky, Stefan ; Westhoff, Niklas ; Hardenberg, Jost von ; Nuhn, Philipp ; Erben, Philipp ; Michel, Maurice Stephan ; Boutros, Michael</creatorcontrib><description>Extracellular vesicles (EVs) are shed by many different cell types. Their nucleic acids content offers new opportunities for biomarker research in different solid tumors. The role of EV RNA in prostate cancer (PCa) is still largely unknown. EVs were isolated from different benign and malignant prostate cell lines and blood plasma from patients with PCa ( = 18) and controls with benign prostatic hyperplasia (BPH) ( = 7). Nanoparticle tracking analysis (NTA), Western blot, electron microscopy, and flow cytometry analysis were used for the characterization of EVs. Non-coding RNA expression profiling of PC3 metastatic PCa cells and their EVs was performed by next generation sequencing (NGS). miRNAs differentially expressed in PC3 EVs were validated with qRT-PCR in EVs derived from additional cell lines and patient plasma and from matched tissue samples. 92 miRNAs were enriched and 48 miRNAs were depleted in PC3 EVs compared to PC3 cells, which could be confirmed by qRT-PCR. miR-99b-5p was significantly higher expressed in malignant compared to benign EVs. Furthermore, expression profiling showed miR-10a-5p ( = 0.018) and miR-29b-3p ( = 0.002), but not miR-99b-5p, to be overexpressed in plasma-derived EVs from patients with PCa compared with controls. In the corresponding tissue samples, no significant differences in the miRNA expression could be observed. We thus propose that EV-associated miR-10a-5p and miR-29b-3p could serve as potential new PCa detection markers.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers12010043</identifier><identifier>PMID: 31877768</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Biomarkers ; Cell culture ; Electron microscopy ; Flow cytometry ; Hyperplasia ; Metastases ; Metastasis ; miRNA ; Nanoparticles ; Next-generation sequencing ; Non-coding RNA ; Prostate cancer ; Proteins ; Solid tumors</subject><ispartof>Cancers, 2019-12, Vol.12 (1), p.43</ispartof><rights>2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 by the authors. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-7efbf0abc5fbf3d2b62c74c918767d04499e6c4400bf7632b3721933936c78ef3</citedby><cites>FETCH-LOGICAL-c421t-7efbf0abc5fbf3d2b62c74c918767d04499e6c4400bf7632b3721933936c78ef3</cites><orcidid>0000-0002-8939-5664 ; 0000-0003-2621-0703 ; 0000-0001-5629-4368 ; 0000-0002-8279-7636 ; 0000-0002-0728-681X ; 0000-0002-7647-7265 ; 0000-0001-5429-126X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017198/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017198/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31877768$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Worst, Thomas Stefan</creatorcontrib><creatorcontrib>Previti, Christopher</creatorcontrib><creatorcontrib>Nitschke, Katja</creatorcontrib><creatorcontrib>Diessl, Nicolle</creatorcontrib><creatorcontrib>Gross, Julia Christina</creatorcontrib><creatorcontrib>Hoffmann, Lena</creatorcontrib><creatorcontrib>Frey, Lisa</creatorcontrib><creatorcontrib>Thomas, Vanessa</creatorcontrib><creatorcontrib>Kahlert, Christoph</creatorcontrib><creatorcontrib>Bieback, Karen</creatorcontrib><creatorcontrib>Crigna, Adriana Torres</creatorcontrib><creatorcontrib>Fricke, Fabia</creatorcontrib><creatorcontrib>Porubsky, Stefan</creatorcontrib><creatorcontrib>Westhoff, Niklas</creatorcontrib><creatorcontrib>Hardenberg, Jost von</creatorcontrib><creatorcontrib>Nuhn, Philipp</creatorcontrib><creatorcontrib>Erben, Philipp</creatorcontrib><creatorcontrib>Michel, Maurice Stephan</creatorcontrib><creatorcontrib>Boutros, Michael</creatorcontrib><title>miR-10a-5p and miR-29b-3p as Extracellular Vesicle-Associated Prostate Cancer Detection Markers</title><title>Cancers</title><addtitle>Cancers (Basel)</addtitle><description>Extracellular vesicles (EVs) are shed by many different cell types. Their nucleic acids content offers new opportunities for biomarker research in different solid tumors. The role of EV RNA in prostate cancer (PCa) is still largely unknown. EVs were isolated from different benign and malignant prostate cell lines and blood plasma from patients with PCa ( = 18) and controls with benign prostatic hyperplasia (BPH) ( = 7). Nanoparticle tracking analysis (NTA), Western blot, electron microscopy, and flow cytometry analysis were used for the characterization of EVs. Non-coding RNA expression profiling of PC3 metastatic PCa cells and their EVs was performed by next generation sequencing (NGS). miRNAs differentially expressed in PC3 EVs were validated with qRT-PCR in EVs derived from additional cell lines and patient plasma and from matched tissue samples. 92 miRNAs were enriched and 48 miRNAs were depleted in PC3 EVs compared to PC3 cells, which could be confirmed by qRT-PCR. miR-99b-5p was significantly higher expressed in malignant compared to benign EVs. Furthermore, expression profiling showed miR-10a-5p ( = 0.018) and miR-29b-3p ( = 0.002), but not miR-99b-5p, to be overexpressed in plasma-derived EVs from patients with PCa compared with controls. In the corresponding tissue samples, no significant differences in the miRNA expression could be observed. We thus propose that EV-associated miR-10a-5p and miR-29b-3p could serve as potential new PCa detection markers.</description><subject>Biomarkers</subject><subject>Cell culture</subject><subject>Electron microscopy</subject><subject>Flow cytometry</subject><subject>Hyperplasia</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>miRNA</subject><subject>Nanoparticles</subject><subject>Next-generation sequencing</subject><subject>Non-coding RNA</subject><subject>Prostate cancer</subject><subject>Proteins</subject><subject>Solid tumors</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdUU1LAzEUDKLYoj17kwUvXmLztcnmIpT6CRVF1GvIZrO6dbupya7ovze1tdTm8t7jTYaZeQAcYXRGqURDoxtjfcAEYYQY3QF9ggSBnEu2u9H3wCCEKYqPUiy42Ac9ijMhBM_6QM2qR4iRhuk80U2RLEYic0jjGJLLr9ZrY-u6q7VPXmyoTG3hKARnKt3aInnwLrSxS8a_WpIL21rTVq5J7rR_j-IOwV6p62AHq3oAnq8un8Y3cHJ_fTseTaBhBLdQ2DIvkc5NGistSM6JEczIqJOLAjEmpeWGMYTyUnBKcioIljEFyo3IbEkPwPmSd97lM1sY20TltZr7aqb9t3K6Uv83TfWmXt2nEggLLLNIcLoi8O6js6GNyYSFdd1Y1wVFYngkJSlGEXqyBZ26zjfRniIpExzJTJCIGi5RJmYUvC3XYjBSi_uprfvFH8ebHtb4v2vRH1nNllw</recordid><startdate>20191221</startdate><enddate>20191221</enddate><creator>Worst, Thomas Stefan</creator><creator>Previti, Christopher</creator><creator>Nitschke, Katja</creator><creator>Diessl, Nicolle</creator><creator>Gross, Julia Christina</creator><creator>Hoffmann, Lena</creator><creator>Frey, Lisa</creator><creator>Thomas, Vanessa</creator><creator>Kahlert, Christoph</creator><creator>Bieback, Karen</creator><creator>Crigna, Adriana Torres</creator><creator>Fricke, Fabia</creator><creator>Porubsky, Stefan</creator><creator>Westhoff, Niklas</creator><creator>Hardenberg, Jost von</creator><creator>Nuhn, Philipp</creator><creator>Erben, Philipp</creator><creator>Michel, Maurice Stephan</creator><creator>Boutros, Michael</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</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>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</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><orcidid>https://orcid.org/0000-0002-8939-5664</orcidid><orcidid>https://orcid.org/0000-0003-2621-0703</orcidid><orcidid>https://orcid.org/0000-0001-5629-4368</orcidid><orcidid>https://orcid.org/0000-0002-8279-7636</orcidid><orcidid>https://orcid.org/0000-0002-0728-681X</orcidid><orcidid>https://orcid.org/0000-0002-7647-7265</orcidid><orcidid>https://orcid.org/0000-0001-5429-126X</orcidid></search><sort><creationdate>20191221</creationdate><title>miR-10a-5p and miR-29b-3p as Extracellular Vesicle-Associated Prostate Cancer Detection Markers</title><author>Worst, Thomas Stefan ; Previti, Christopher ; Nitschke, Katja ; Diessl, Nicolle ; Gross, Julia Christina ; Hoffmann, Lena ; Frey, Lisa ; Thomas, Vanessa ; Kahlert, Christoph ; Bieback, Karen ; Crigna, Adriana Torres ; Fricke, Fabia ; Porubsky, Stefan ; Westhoff, Niklas ; Hardenberg, Jost von ; Nuhn, Philipp ; Erben, Philipp ; Michel, Maurice Stephan ; Boutros, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-7efbf0abc5fbf3d2b62c74c918767d04499e6c4400bf7632b3721933936c78ef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Biomarkers</topic><topic>Cell culture</topic><topic>Electron microscopy</topic><topic>Flow cytometry</topic><topic>Hyperplasia</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>miRNA</topic><topic>Nanoparticles</topic><topic>Next-generation sequencing</topic><topic>Non-coding RNA</topic><topic>Prostate cancer</topic><topic>Proteins</topic><topic>Solid tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Worst, Thomas Stefan</creatorcontrib><creatorcontrib>Previti, Christopher</creatorcontrib><creatorcontrib>Nitschke, Katja</creatorcontrib><creatorcontrib>Diessl, Nicolle</creatorcontrib><creatorcontrib>Gross, Julia Christina</creatorcontrib><creatorcontrib>Hoffmann, Lena</creatorcontrib><creatorcontrib>Frey, Lisa</creatorcontrib><creatorcontrib>Thomas, Vanessa</creatorcontrib><creatorcontrib>Kahlert, Christoph</creatorcontrib><creatorcontrib>Bieback, Karen</creatorcontrib><creatorcontrib>Crigna, Adriana Torres</creatorcontrib><creatorcontrib>Fricke, Fabia</creatorcontrib><creatorcontrib>Porubsky, Stefan</creatorcontrib><creatorcontrib>Westhoff, Niklas</creatorcontrib><creatorcontrib>Hardenberg, Jost von</creatorcontrib><creatorcontrib>Nuhn, Philipp</creatorcontrib><creatorcontrib>Erben, Philipp</creatorcontrib><creatorcontrib>Michel, Maurice Stephan</creatorcontrib><creatorcontrib>Boutros, Michael</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</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>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</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><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Worst, Thomas Stefan</au><au>Previti, Christopher</au><au>Nitschke, Katja</au><au>Diessl, Nicolle</au><au>Gross, Julia Christina</au><au>Hoffmann, Lena</au><au>Frey, Lisa</au><au>Thomas, Vanessa</au><au>Kahlert, Christoph</au><au>Bieback, Karen</au><au>Crigna, Adriana Torres</au><au>Fricke, Fabia</au><au>Porubsky, Stefan</au><au>Westhoff, Niklas</au><au>Hardenberg, Jost von</au><au>Nuhn, Philipp</au><au>Erben, Philipp</au><au>Michel, Maurice Stephan</au><au>Boutros, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>miR-10a-5p and miR-29b-3p as Extracellular Vesicle-Associated Prostate Cancer Detection Markers</atitle><jtitle>Cancers</jtitle><addtitle>Cancers (Basel)</addtitle><date>2019-12-21</date><risdate>2019</risdate><volume>12</volume><issue>1</issue><spage>43</spage><pages>43-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>Extracellular vesicles (EVs) are shed by many different cell types. Their nucleic acids content offers new opportunities for biomarker research in different solid tumors. The role of EV RNA in prostate cancer (PCa) is still largely unknown. EVs were isolated from different benign and malignant prostate cell lines and blood plasma from patients with PCa ( = 18) and controls with benign prostatic hyperplasia (BPH) ( = 7). Nanoparticle tracking analysis (NTA), Western blot, electron microscopy, and flow cytometry analysis were used for the characterization of EVs. Non-coding RNA expression profiling of PC3 metastatic PCa cells and their EVs was performed by next generation sequencing (NGS). miRNAs differentially expressed in PC3 EVs were validated with qRT-PCR in EVs derived from additional cell lines and patient plasma and from matched tissue samples. 92 miRNAs were enriched and 48 miRNAs were depleted in PC3 EVs compared to PC3 cells, which could be confirmed by qRT-PCR. miR-99b-5p was significantly higher expressed in malignant compared to benign EVs. Furthermore, expression profiling showed miR-10a-5p ( = 0.018) and miR-29b-3p ( = 0.002), but not miR-99b-5p, to be overexpressed in plasma-derived EVs from patients with PCa compared with controls. In the corresponding tissue samples, no significant differences in the miRNA expression could be observed. We thus propose that EV-associated miR-10a-5p and miR-29b-3p could serve as potential new PCa detection markers.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>31877768</pmid><doi>10.3390/cancers12010043</doi><orcidid>https://orcid.org/0000-0002-8939-5664</orcidid><orcidid>https://orcid.org/0000-0003-2621-0703</orcidid><orcidid>https://orcid.org/0000-0001-5629-4368</orcidid><orcidid>https://orcid.org/0000-0002-8279-7636</orcidid><orcidid>https://orcid.org/0000-0002-0728-681X</orcidid><orcidid>https://orcid.org/0000-0002-7647-7265</orcidid><orcidid>https://orcid.org/0000-0001-5429-126X</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2072-6694
ispartof Cancers, 2019-12, Vol.12 (1), p.43
issn 2072-6694
2072-6694
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7017198
source MDPI - Multidisciplinary Digital Publishing Institute; EZB-FREE-00999 freely available EZB journals; PubMed Central; PubMed Central Open Access
subjects Biomarkers
Cell culture
Electron microscopy
Flow cytometry
Hyperplasia
Metastases
Metastasis
miRNA
Nanoparticles
Next-generation sequencing
Non-coding RNA
Prostate cancer
Proteins
Solid tumors
title miR-10a-5p and miR-29b-3p as Extracellular Vesicle-Associated Prostate Cancer Detection Markers
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T12%3A37%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=miR-10a-5p%20and%20miR-29b-3p%20as%20Extracellular%20Vesicle-Associated%20Prostate%20Cancer%20Detection%20Markers&rft.jtitle=Cancers&rft.au=Worst,%20Thomas%20Stefan&rft.date=2019-12-21&rft.volume=12&rft.issue=1&rft.spage=43&rft.pages=43-&rft.issn=2072-6694&rft.eissn=2072-6694&rft_id=info:doi/10.3390/cancers12010043&rft_dat=%3Cproquest_pubme%3E2547609872%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2547609872&rft_id=info:pmid/31877768&rfr_iscdi=true