Accurate and sensitive dual-response fluorescence detection of microRNAs based on an upconversion nanoamplicon with red emission
Oral squamous cell carcinoma (OSCC) is the most common type of oral cancer. In recent years, researchers have found a close relationship between microRNAs (miRNAs) and OSCC. In addition, miRNAs are highly stable in tissues and circulation, and are also considered potential biomarkers for cancer dete...
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description | Oral squamous cell carcinoma (OSCC) is the most common type of oral cancer. In recent years, researchers have found a close relationship between microRNAs (miRNAs) and OSCC. In addition, miRNAs are highly stable in tissues and circulation, and are also considered potential biomarkers for cancer detection and prognosis. Among a variety of tools for miRNAs with low abundance, single red-emitting UCNP-based biosensors have attracted special interest due to their unique properties, including deep organizational penetration, weak radiation damage, and low autofluorescence. Additionally, the measurement of low-abundance analytes
via
enzyme-free signal amplification is also an effective means. Herein, by taking advantage of red-emitting UCNPs and an enzyme-toehold-mediated strand displacement cascade, a dual-signal amplification biosensor was constructed. The recycled miRNA can be regarded as a catalyst for the assembly of multiple H1/H2 duplexes, which promoted the response signal of augmented analyte expression. Moreover, the proposed biosensors improved the measurement accuracy
via
a dual-signal response to obviously avert false-positive signals. The proposed method was applied to measure miRNA-222 (a model analyte) in serum samples, and the results were similar to those of polymerase chain reaction (PCR), with spiked recoveries ranging from 91.2% to 101.7%. The proposed assay has the merits of high sensitivity, strong recognition, and low background, indicating broad potential for the measurement of diverse analytes in biological samples.
Oral squamous cell carcinoma (OSCC) is the most common type of oral cancer. |
doi_str_mv | 10.1039/d4ra05061d |
format | Article |
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via
enzyme-free signal amplification is also an effective means. Herein, by taking advantage of red-emitting UCNPs and an enzyme-toehold-mediated strand displacement cascade, a dual-signal amplification biosensor was constructed. The recycled miRNA can be regarded as a catalyst for the assembly of multiple H1/H2 duplexes, which promoted the response signal of augmented analyte expression. Moreover, the proposed biosensors improved the measurement accuracy
via
a dual-signal response to obviously avert false-positive signals. The proposed method was applied to measure miRNA-222 (a model analyte) in serum samples, and the results were similar to those of polymerase chain reaction (PCR), with spiked recoveries ranging from 91.2% to 101.7%. The proposed assay has the merits of high sensitivity, strong recognition, and low background, indicating broad potential for the measurement of diverse analytes in biological samples.
Oral squamous cell carcinoma (OSCC) is the most common type of oral cancer.</description><identifier>ISSN: 2046-2069</identifier><identifier>EISSN: 2046-2069</identifier><identifier>DOI: 10.1039/d4ra05061d</identifier><identifier>PMID: 39429926</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Biological properties ; Biomarkers ; Biosensors ; Cancer ; Enzymes ; MicroRNAs ; Polymerase chain reaction ; Radiation damage ; Sensitivity analysis</subject><ispartof>RSC advances, 2024-10, Vol.14 (45), p.32911-32921</ispartof><rights>This journal is © The Royal Society of Chemistry.</rights><rights>Copyright Royal Society of Chemistry 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c262t-260917079ca89ad7fe65cf37606cfe5cddc858343908b2ddd9c1d71fdf33b6a83</cites><orcidid>0009-0003-3703-6779</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,861,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39429926$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Lingling</creatorcontrib><creatorcontrib>Zhou, Yi</creatorcontrib><creatorcontrib>Xu, Liang</creatorcontrib><creatorcontrib>Ruan, Xin</creatorcontrib><creatorcontrib>Huang, Zhao</creatorcontrib><creatorcontrib>Ke, Yue</creatorcontrib><creatorcontrib>Lin, Lisong</creatorcontrib><creatorcontrib>Tang, Qiuling</creatorcontrib><title>Accurate and sensitive dual-response fluorescence detection of microRNAs based on an upconversion nanoamplicon with red emission</title><title>RSC advances</title><addtitle>RSC Adv</addtitle><description>Oral squamous cell carcinoma (OSCC) is the most common type of oral cancer. In recent years, researchers have found a close relationship between microRNAs (miRNAs) and OSCC. In addition, miRNAs are highly stable in tissues and circulation, and are also considered potential biomarkers for cancer detection and prognosis. Among a variety of tools for miRNAs with low abundance, single red-emitting UCNP-based biosensors have attracted special interest due to their unique properties, including deep organizational penetration, weak radiation damage, and low autofluorescence. Additionally, the measurement of low-abundance analytes
via
enzyme-free signal amplification is also an effective means. Herein, by taking advantage of red-emitting UCNPs and an enzyme-toehold-mediated strand displacement cascade, a dual-signal amplification biosensor was constructed. The recycled miRNA can be regarded as a catalyst for the assembly of multiple H1/H2 duplexes, which promoted the response signal of augmented analyte expression. Moreover, the proposed biosensors improved the measurement accuracy
via
a dual-signal response to obviously avert false-positive signals. The proposed method was applied to measure miRNA-222 (a model analyte) in serum samples, and the results were similar to those of polymerase chain reaction (PCR), with spiked recoveries ranging from 91.2% to 101.7%. The proposed assay has the merits of high sensitivity, strong recognition, and low background, indicating broad potential for the measurement of diverse analytes in biological samples.
Oral squamous cell carcinoma (OSCC) is the most common type of oral cancer.</description><subject>Biological properties</subject><subject>Biomarkers</subject><subject>Biosensors</subject><subject>Cancer</subject><subject>Enzymes</subject><subject>MicroRNAs</subject><subject>Polymerase chain reaction</subject><subject>Radiation damage</subject><subject>Sensitivity analysis</subject><issn>2046-2069</issn><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpd0c9r2zAUB3BRWprQ5bL7iqCXMvCmH7YsHUPadYPQQtjORpGemIMtuZLd0tv-9ClN15bpoh_vw-OhL0IfKflCCVdfbRk1qYig9gjNGSlFwYhQx-_OM7RIaUfyEhVlgp6iGVclU4qJOfqzNGaKegSsvcUJfGrH9gGwnXRXREhD8Amw66aQLwa8ySUYwYxt8Dg43Lcmhs3tMuGtTmBxftUeT4MJ_gFi2iuvfdD90LX5DT-2428cM4S-TfvyB3TidJdg8bKfoV_frn-uvhfru5sfq-W6MEywsWCCKFqTWhktlba1A1EZx2tBhHFQGWuNrCQvuSJyy6y1ylBbU2cd51uhJT9Dl4e-Qwz3E6SxyQMY6DrtIUyp4ZRKyUUlVaYX_9FdmKLP02XFylIoJausPh9U_oCUIrhmiG2v41NDSbOPprkqN8vnaK4yPn9pOW17sK_0XxAZfDqAmMxr9S1b_hedJpTq</recordid><startdate>20241017</startdate><enddate>20241017</enddate><creator>Huang, Lingling</creator><creator>Zhou, Yi</creator><creator>Xu, Liang</creator><creator>Ruan, Xin</creator><creator>Huang, Zhao</creator><creator>Ke, Yue</creator><creator>Lin, Lisong</creator><creator>Tang, Qiuling</creator><general>Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><orcidid>https://orcid.org/0009-0003-3703-6779</orcidid></search><sort><creationdate>20241017</creationdate><title>Accurate and sensitive dual-response fluorescence detection of microRNAs based on an upconversion nanoamplicon with red emission</title><author>Huang, Lingling ; Zhou, Yi ; Xu, Liang ; Ruan, Xin ; Huang, Zhao ; Ke, Yue ; Lin, Lisong ; Tang, Qiuling</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c262t-260917079ca89ad7fe65cf37606cfe5cddc858343908b2ddd9c1d71fdf33b6a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Biological properties</topic><topic>Biomarkers</topic><topic>Biosensors</topic><topic>Cancer</topic><topic>Enzymes</topic><topic>MicroRNAs</topic><topic>Polymerase chain reaction</topic><topic>Radiation damage</topic><topic>Sensitivity analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Lingling</creatorcontrib><creatorcontrib>Zhou, Yi</creatorcontrib><creatorcontrib>Xu, Liang</creatorcontrib><creatorcontrib>Ruan, Xin</creatorcontrib><creatorcontrib>Huang, Zhao</creatorcontrib><creatorcontrib>Ke, Yue</creatorcontrib><creatorcontrib>Lin, Lisong</creatorcontrib><creatorcontrib>Tang, Qiuling</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><jtitle>RSC advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Lingling</au><au>Zhou, Yi</au><au>Xu, Liang</au><au>Ruan, Xin</au><au>Huang, Zhao</au><au>Ke, Yue</au><au>Lin, Lisong</au><au>Tang, Qiuling</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Accurate and sensitive dual-response fluorescence detection of microRNAs based on an upconversion nanoamplicon with red emission</atitle><jtitle>RSC advances</jtitle><addtitle>RSC Adv</addtitle><date>2024-10-17</date><risdate>2024</risdate><volume>14</volume><issue>45</issue><spage>32911</spage><epage>32921</epage><pages>32911-32921</pages><issn>2046-2069</issn><eissn>2046-2069</eissn><abstract>Oral squamous cell carcinoma (OSCC) is the most common type of oral cancer. In recent years, researchers have found a close relationship between microRNAs (miRNAs) and OSCC. In addition, miRNAs are highly stable in tissues and circulation, and are also considered potential biomarkers for cancer detection and prognosis. Among a variety of tools for miRNAs with low abundance, single red-emitting UCNP-based biosensors have attracted special interest due to their unique properties, including deep organizational penetration, weak radiation damage, and low autofluorescence. Additionally, the measurement of low-abundance analytes
via
enzyme-free signal amplification is also an effective means. Herein, by taking advantage of red-emitting UCNPs and an enzyme-toehold-mediated strand displacement cascade, a dual-signal amplification biosensor was constructed. The recycled miRNA can be regarded as a catalyst for the assembly of multiple H1/H2 duplexes, which promoted the response signal of augmented analyte expression. Moreover, the proposed biosensors improved the measurement accuracy
via
a dual-signal response to obviously avert false-positive signals. The proposed method was applied to measure miRNA-222 (a model analyte) in serum samples, and the results were similar to those of polymerase chain reaction (PCR), with spiked recoveries ranging from 91.2% to 101.7%. The proposed assay has the merits of high sensitivity, strong recognition, and low background, indicating broad potential for the measurement of diverse analytes in biological samples.
Oral squamous cell carcinoma (OSCC) is the most common type of oral cancer.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>39429926</pmid><doi>10.1039/d4ra05061d</doi><tpages>11</tpages><orcidid>https://orcid.org/0009-0003-3703-6779</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biological properties Biomarkers Biosensors Cancer Enzymes MicroRNAs Polymerase chain reaction Radiation damage Sensitivity analysis |
title | Accurate and sensitive dual-response fluorescence detection of microRNAs based on an upconversion nanoamplicon with red emission |
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