Tumor-derived EV miRNA signatures surpass total EV miRNA in supplementing mammography for precision breast cancer diagnosis
With the rising global incidence and mortality rates of breast cancer, early diagnosis is becoming increasingly crucial. The World Health Organization (WHO) recommends mammography as a primary screening tool. However, despite its clinical benefits, mammography has potential risks including radiation...
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description | With the rising global incidence and mortality rates of breast cancer, early diagnosis is becoming increasingly crucial. The World Health Organization (WHO) recommends mammography as a primary screening tool. However, despite its clinical benefits, mammography has potential risks including radiation exposure, unnecessary follow-up, and overdiagnosis due to false positives, particularly in cases of early cancer or dense breast tissue. In this study, we aimed to address these concerns by introducing an innovative diagnostic method that employs circulating biomarkers to enhance the existing screening techniques
Breast cancer-derived extracellular vesicles (BEVs) were isolated from the bloodstream using advanced immunoaffinity capture techniques. Subsequently, we analyzed the microRNA (miRNA) profiles of BEVs in plasma samples from 120 patients with breast cancer, 46 with benign tumors, and 45 healthy controls.
This retrospective study identified a distinct signature of five EV miRNAs (miR-21, miR-106b, miR-181a, miR-484, and miR-1260b) that effectively differentiated patients with breast cancer from healthy controls. This signature provides essential insights into tumor progression, metastasis, and the risk of recurrence. Notably, overexpression of this signature correlated with poorer survival outcomes.
Our novel gene signature-based approach not only complements existing diagnostic methods with high accuracy but also provides a deeper understanding of the molecular aspects of breast cancer, heralding a significant advancement in precision medicine and personalized cancer care. |
doi_str_mv | 10.7150/thno.99245 |
format | Article |
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Breast cancer-derived extracellular vesicles (BEVs) were isolated from the bloodstream using advanced immunoaffinity capture techniques. Subsequently, we analyzed the microRNA (miRNA) profiles of BEVs in plasma samples from 120 patients with breast cancer, 46 with benign tumors, and 45 healthy controls.
This retrospective study identified a distinct signature of five EV miRNAs (miR-21, miR-106b, miR-181a, miR-484, and miR-1260b) that effectively differentiated patients with breast cancer from healthy controls. This signature provides essential insights into tumor progression, metastasis, and the risk of recurrence. Notably, overexpression of this signature correlated with poorer survival outcomes.
Our novel gene signature-based approach not only complements existing diagnostic methods with high accuracy but also provides a deeper understanding of the molecular aspects of breast cancer, heralding a significant advancement in precision medicine and personalized cancer care.</description><identifier>ISSN: 1838-7640</identifier><identifier>EISSN: 1838-7640</identifier><identifier>DOI: 10.7150/thno.99245</identifier><identifier>PMID: 39479442</identifier><language>eng</language><publisher>Australia: Ivyspring International Publisher</publisher><subject>Adult ; Aged ; Biomarkers, Tumor - genetics ; Breast Neoplasms - diagnosis ; Breast Neoplasms - diagnostic imaging ; Breast Neoplasms - genetics ; Case-Control Studies ; Early Detection of Cancer - methods ; Extracellular Vesicles - genetics ; Extracellular Vesicles - metabolism ; Female ; Humans ; Mammography - methods ; MicroRNAs - blood ; MicroRNAs - genetics ; Middle Aged ; Precision Medicine - methods ; Research Paper ; Retrospective Studies</subject><ispartof>Theranostics, 2024-01, Vol.14 (17), p.6587-6604</ispartof><rights>The author(s).</rights><rights>The author(s) 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11519808/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11519808/$$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/39479442$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Young</creatorcontrib><creatorcontrib>Kim, Jee Ye</creatorcontrib><creatorcontrib>Moon, Sol</creatorcontrib><creatorcontrib>Lee, Hyojung</creatorcontrib><creatorcontrib>Lee, Suji</creatorcontrib><creatorcontrib>Kim, Joon Ye</creatorcontrib><creatorcontrib>Kim, Min Woo</creatorcontrib><creatorcontrib>Kim, Seung Il</creatorcontrib><title>Tumor-derived EV miRNA signatures surpass total EV miRNA in supplementing mammography for precision breast cancer diagnosis</title><title>Theranostics</title><addtitle>Theranostics</addtitle><description>With the rising global incidence and mortality rates of breast cancer, early diagnosis is becoming increasingly crucial. The World Health Organization (WHO) recommends mammography as a primary screening tool. However, despite its clinical benefits, mammography has potential risks including radiation exposure, unnecessary follow-up, and overdiagnosis due to false positives, particularly in cases of early cancer or dense breast tissue. In this study, we aimed to address these concerns by introducing an innovative diagnostic method that employs circulating biomarkers to enhance the existing screening techniques
Breast cancer-derived extracellular vesicles (BEVs) were isolated from the bloodstream using advanced immunoaffinity capture techniques. Subsequently, we analyzed the microRNA (miRNA) profiles of BEVs in plasma samples from 120 patients with breast cancer, 46 with benign tumors, and 45 healthy controls.
This retrospective study identified a distinct signature of five EV miRNAs (miR-21, miR-106b, miR-181a, miR-484, and miR-1260b) that effectively differentiated patients with breast cancer from healthy controls. This signature provides essential insights into tumor progression, metastasis, and the risk of recurrence. Notably, overexpression of this signature correlated with poorer survival outcomes.
Our novel gene signature-based approach not only complements existing diagnostic methods with high accuracy but also provides a deeper understanding of the molecular aspects of breast cancer, heralding a significant advancement in precision medicine and personalized cancer care.</description><subject>Adult</subject><subject>Aged</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Breast Neoplasms - diagnosis</subject><subject>Breast Neoplasms - diagnostic imaging</subject><subject>Breast Neoplasms - genetics</subject><subject>Case-Control Studies</subject><subject>Early Detection of Cancer - methods</subject><subject>Extracellular Vesicles - genetics</subject><subject>Extracellular Vesicles - metabolism</subject><subject>Female</subject><subject>Humans</subject><subject>Mammography - methods</subject><subject>MicroRNAs - blood</subject><subject>MicroRNAs - genetics</subject><subject>Middle Aged</subject><subject>Precision Medicine - methods</subject><subject>Research Paper</subject><subject>Retrospective Studies</subject><issn>1838-7640</issn><issn>1838-7640</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkV1rFjEQhYMottTe-AMklyJszddmkysppbZCUSittyGbnewb2SRrslso_vluP6x1bmbgPJw5cBB6T8lRR1vyedmlfKQ1E-0rtE8VV00nBXn94t5Dh7X-ItsIwjTVb9Ee16LTQrB99Odqjbk0A5RwAwM-_YljuPx-jGsYk13WAhXXtcy2VrzkxU7_iJA2ZZ4niJCWkEYcbYx5LHbe3WKfC54LuFBDTrgvYOuCnU0OCh6CHVOuob5Db7ydKhw-7QN0_fX06uS8ufhx9u3k-KJxTKql6XrOmfaqFaIF7qjvOqaUIF2vPXiqtPfKcbLJ0FMlSU8kDIq5tpetVE7yA_Tl0Xde-wiD2_IWO5m5hGjLrck2mP-VFHZmzDeG0pZqRdTm8PHJoeTfK9TFxFAdTJNNkNdqOGVMCklEt6GfHlFXcq0F_PMfSsx9Y-a-MfPQ2AZ_eJnsGf3bD78DU8GUOA</recordid><startdate>20240101</startdate><enddate>20240101</enddate><creator>Kim, Young</creator><creator>Kim, Jee Ye</creator><creator>Moon, Sol</creator><creator>Lee, Hyojung</creator><creator>Lee, Suji</creator><creator>Kim, Joon Ye</creator><creator>Kim, Min Woo</creator><creator>Kim, Seung Il</creator><general>Ivyspring International Publisher</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20240101</creationdate><title>Tumor-derived EV miRNA signatures surpass total EV miRNA in supplementing mammography for precision breast cancer diagnosis</title><author>Kim, Young ; Kim, Jee Ye ; Moon, Sol ; Lee, Hyojung ; Lee, Suji ; Kim, Joon Ye ; Kim, Min Woo ; Kim, Seung Il</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c268t-7b3329f85445e3c1f77288407b9fef189ff8c30544eb1860b06ed82c5b6568c63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Breast Neoplasms - diagnosis</topic><topic>Breast Neoplasms - diagnostic imaging</topic><topic>Breast Neoplasms - genetics</topic><topic>Case-Control Studies</topic><topic>Early Detection of Cancer - methods</topic><topic>Extracellular Vesicles - genetics</topic><topic>Extracellular Vesicles - metabolism</topic><topic>Female</topic><topic>Humans</topic><topic>Mammography - methods</topic><topic>MicroRNAs - blood</topic><topic>MicroRNAs - genetics</topic><topic>Middle Aged</topic><topic>Precision Medicine - methods</topic><topic>Research Paper</topic><topic>Retrospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Young</creatorcontrib><creatorcontrib>Kim, Jee Ye</creatorcontrib><creatorcontrib>Moon, Sol</creatorcontrib><creatorcontrib>Lee, Hyojung</creatorcontrib><creatorcontrib>Lee, Suji</creatorcontrib><creatorcontrib>Kim, Joon Ye</creatorcontrib><creatorcontrib>Kim, Min Woo</creatorcontrib><creatorcontrib>Kim, Seung Il</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Theranostics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Young</au><au>Kim, Jee Ye</au><au>Moon, Sol</au><au>Lee, Hyojung</au><au>Lee, Suji</au><au>Kim, Joon Ye</au><au>Kim, Min Woo</au><au>Kim, Seung Il</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tumor-derived EV miRNA signatures surpass total EV miRNA in supplementing mammography for precision breast cancer diagnosis</atitle><jtitle>Theranostics</jtitle><addtitle>Theranostics</addtitle><date>2024-01-01</date><risdate>2024</risdate><volume>14</volume><issue>17</issue><spage>6587</spage><epage>6604</epage><pages>6587-6604</pages><issn>1838-7640</issn><eissn>1838-7640</eissn><abstract>With the rising global incidence and mortality rates of breast cancer, early diagnosis is becoming increasingly crucial. The World Health Organization (WHO) recommends mammography as a primary screening tool. However, despite its clinical benefits, mammography has potential risks including radiation exposure, unnecessary follow-up, and overdiagnosis due to false positives, particularly in cases of early cancer or dense breast tissue. In this study, we aimed to address these concerns by introducing an innovative diagnostic method that employs circulating biomarkers to enhance the existing screening techniques
Breast cancer-derived extracellular vesicles (BEVs) were isolated from the bloodstream using advanced immunoaffinity capture techniques. Subsequently, we analyzed the microRNA (miRNA) profiles of BEVs in plasma samples from 120 patients with breast cancer, 46 with benign tumors, and 45 healthy controls.
This retrospective study identified a distinct signature of five EV miRNAs (miR-21, miR-106b, miR-181a, miR-484, and miR-1260b) that effectively differentiated patients with breast cancer from healthy controls. This signature provides essential insights into tumor progression, metastasis, and the risk of recurrence. Notably, overexpression of this signature correlated with poorer survival outcomes.
Our novel gene signature-based approach not only complements existing diagnostic methods with high accuracy but also provides a deeper understanding of the molecular aspects of breast cancer, heralding a significant advancement in precision medicine and personalized cancer care.</abstract><cop>Australia</cop><pub>Ivyspring International Publisher</pub><pmid>39479442</pmid><doi>10.7150/thno.99245</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Biomarkers, Tumor - genetics Breast Neoplasms - diagnosis Breast Neoplasms - diagnostic imaging Breast Neoplasms - genetics Case-Control Studies Early Detection of Cancer - methods Extracellular Vesicles - genetics Extracellular Vesicles - metabolism Female Humans Mammography - methods MicroRNAs - blood MicroRNAs - genetics Middle Aged Precision Medicine - methods Research Paper Retrospective Studies |
title | Tumor-derived EV miRNA signatures surpass total EV miRNA in supplementing mammography for precision breast cancer diagnosis |
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