Loading…

A novel malic acid-enhanced method for the analysis of 5-methyl-2′-deoxycytidine, 5-hydroxymethyl-2′-deoxycytidine, 5-methylcytidine and 5-hydroxymethylcytidine in human urine using hydrophilic interaction liquid chromatography-tandem mass spectrometry

5-Methyl-2′-deoxycytidine (5-mdC), 5-hydroxymethyl-2′-deoxycytidine (5-hmdC), 5-methylcytidine (5-mrC) and 5-hydroxymethylcytidine (5-hmrC) are epigenetic marks of DNA and RNA, and aberrant levels of these modified nucleosides were found to be associated with various cancers. Urine is a preferred so...

Full description

Saved in:
Bibliographic Details
Published in:Analytica chimica acta 2018-11, Vol.1034, p.110-118
Main Authors: Guo, Cheng, Xie, Cong, Chen, Qin, Cao, Xiaoji, Guo, Mengzhe, Zheng, Shu, Wang, Yinsheng
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c479t-b3c9ef8b953d5c0c2fa748c7a5b6596e4c403c7902133fc9d4503609fda294e63
cites cdi_FETCH-LOGICAL-c479t-b3c9ef8b953d5c0c2fa748c7a5b6596e4c403c7902133fc9d4503609fda294e63
container_end_page 118
container_issue
container_start_page 110
container_title Analytica chimica acta
container_volume 1034
creator Guo, Cheng
Xie, Cong
Chen, Qin
Cao, Xiaoji
Guo, Mengzhe
Zheng, Shu
Wang, Yinsheng
description 5-Methyl-2′-deoxycytidine (5-mdC), 5-hydroxymethyl-2′-deoxycytidine (5-hmdC), 5-methylcytidine (5-mrC) and 5-hydroxymethylcytidine (5-hmrC) are epigenetic marks of DNA and RNA, and aberrant levels of these modified nucleosides were found to be associated with various cancers. Urine is a preferred source of biological fluid for biomarker discovery because the sample collection process is not invasive to patients. Herein, we developed a novel malic acid-enhanced hydrophilic interaction liquid chromatography-tandem mass spectrometry (HILIC-MS/MS) method for sensitive and simultaneous quantification of the modified cytosine nucleosides in human urine. Malic acid markedly increased the detection sensitivities of all four cytosine nucleosides, with the limits of detection (LODs) for 5-mdC, 5-hmdC, 5-mrC and 5-hmrC being 0.025, 0.025, 0.025 and 0.050 fmol, respectively. By using this method, we demonstrated, for the first time, the presence of 5-hmrC in human urine, and we successfully quantified 5-mdC, 5-hmdC, 5-mrC and 5-hmrC in urine samples collected from 90 patients with colorectal cancer (CRC) and 90 healthy controls. We found that the levels of 5-mdC, 5-hmdC, 5-mrC and 5-hmrC in urine were all substantially decreased in CRC patients, suggesting that these modified nucleosides might have great potential to be noninvasive biomarkers for early detection and prognosis of CRC. Together, we established a novel and sensitive method for detecting 5-methylated and 5-hydroxymethylated cytosine nucleosides in human urine and the results from this study may stimulate future investigations about the regulatory roles of these cytosine derivatives in the initiation and development of CRC. [Display omitted] •A novel method was reported for analysis of 5-methylated and 5-hydroxymethylated cytosine nucleosides in urine.•Enhancement of detection sensitivity was achieved with the assistance of malic acid.•Accurate quantification was realized by using stable isotope dilution method.•5-hydroxymethylcytidine was firstly discovered in human urine.•The modified cytosine nucleosides are present in significantly lower levels in urine of colorectal cancer patients.
doi_str_mv 10.1016/j.aca.2018.06.081
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6162048</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0003267018308468</els_id><sourcerecordid>2131831537</sourcerecordid><originalsourceid>FETCH-LOGICAL-c479t-b3c9ef8b953d5c0c2fa748c7a5b6596e4c403c7902133fc9d4503609fda294e63</originalsourceid><addsrcrecordid>eNp9ks1u1DAUhQMC0aHwAGyQJTYsSLBjx0mEhFRV_EmV2MDa8tg3E48SO7WdEdnxTDwST4LDtCPooivr-nz3yL73ZNkLgguCCX-7L6SSRYlJU2Be4IY8zDakqWnOaMkeZRuMMc1LXuOz7GkI-1SWBLMn2RnFpKW8ZJsH2QWy7gADGuVgFJLK6BxsL60CjUaIvdOocx7FHpC0cliCCch1qMpXcRny8vfPX7kG92NRSzTaWHiTxH7RPl3dyxzF25vkru82njRjUT-P0qLZr-UcjN2hv-jUm_XdxkbwUkXjLBrM9Ww0Ur13o4xu5-XUL3lM_jCmb4aAwgQqJhWiX55ljzs5BHh-c55n3z9--Hb5Ob_6-unL5cVVrljdxnxLVQtds20rqiuFVdnJmjWqltWWVy0Hphimqm7ThCntVKtZhSnHbadl2TLg9Dx7f_Sd5u0IWoGNXg5i8maUfhFOGvG_Yk0vdu4gOOElZk0yeH1j4N31DCGK0QQFwyAtuDmItFpS8oZWLKGv7qB7N_u0vZWipKGkonWiyJFS3oXgoTs9hmCx5kvsRcqXWPMlMBcpX6nn5b-_OHXcBioB744ApFkeDHgRlIE1TcanoQvtzD32fwCWGOoJ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2131831537</pqid></control><display><type>article</type><title>A novel malic acid-enhanced method for the analysis of 5-methyl-2′-deoxycytidine, 5-hydroxymethyl-2′-deoxycytidine, 5-methylcytidine and 5-hydroxymethylcytidine in human urine using hydrophilic interaction liquid chromatography-tandem mass spectrometry</title><source>ScienceDirect Journals</source><creator>Guo, Cheng ; Xie, Cong ; Chen, Qin ; Cao, Xiaoji ; Guo, Mengzhe ; Zheng, Shu ; Wang, Yinsheng</creator><creatorcontrib>Guo, Cheng ; Xie, Cong ; Chen, Qin ; Cao, Xiaoji ; Guo, Mengzhe ; Zheng, Shu ; Wang, Yinsheng</creatorcontrib><description>5-Methyl-2′-deoxycytidine (5-mdC), 5-hydroxymethyl-2′-deoxycytidine (5-hmdC), 5-methylcytidine (5-mrC) and 5-hydroxymethylcytidine (5-hmrC) are epigenetic marks of DNA and RNA, and aberrant levels of these modified nucleosides were found to be associated with various cancers. Urine is a preferred source of biological fluid for biomarker discovery because the sample collection process is not invasive to patients. Herein, we developed a novel malic acid-enhanced hydrophilic interaction liquid chromatography-tandem mass spectrometry (HILIC-MS/MS) method for sensitive and simultaneous quantification of the modified cytosine nucleosides in human urine. Malic acid markedly increased the detection sensitivities of all four cytosine nucleosides, with the limits of detection (LODs) for 5-mdC, 5-hmdC, 5-mrC and 5-hmrC being 0.025, 0.025, 0.025 and 0.050 fmol, respectively. By using this method, we demonstrated, for the first time, the presence of 5-hmrC in human urine, and we successfully quantified 5-mdC, 5-hmdC, 5-mrC and 5-hmrC in urine samples collected from 90 patients with colorectal cancer (CRC) and 90 healthy controls. We found that the levels of 5-mdC, 5-hmdC, 5-mrC and 5-hmrC in urine were all substantially decreased in CRC patients, suggesting that these modified nucleosides might have great potential to be noninvasive biomarkers for early detection and prognosis of CRC. Together, we established a novel and sensitive method for detecting 5-methylated and 5-hydroxymethylated cytosine nucleosides in human urine and the results from this study may stimulate future investigations about the regulatory roles of these cytosine derivatives in the initiation and development of CRC. [Display omitted] •A novel method was reported for analysis of 5-methylated and 5-hydroxymethylated cytosine nucleosides in urine.•Enhancement of detection sensitivity was achieved with the assistance of malic acid.•Accurate quantification was realized by using stable isotope dilution method.•5-hydroxymethylcytidine was firstly discovered in human urine.•The modified cytosine nucleosides are present in significantly lower levels in urine of colorectal cancer patients.</description><identifier>ISSN: 0003-2670</identifier><identifier>EISSN: 1873-4324</identifier><identifier>DOI: 10.1016/j.aca.2018.06.081</identifier><identifier>PMID: 30193624</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>5-Methylated and 5-hydroxymethylated cytosine nucleosides ; Biomarkers ; Chromatography ; Chromatography, Liquid ; Colorectal cancer ; Colorectal carcinoma ; Cytidine - analogs &amp; derivatives ; Cytidine - chemistry ; Cytidine - urine ; Cytosine ; Deoxycytidine - analogs &amp; derivatives ; Deoxycytidine - chemistry ; Deoxycytidine - urine ; Deoxyribonucleic acid ; DNA ; DNA and RNA modification ; Epigenetics ; Human wastes ; Humans ; Hydrophilic interaction liquid chromatography-tandem mass spectrometry ; Hydrophobic and Hydrophilic Interactions ; Invasiveness ; Liquid chromatography ; Malates - chemistry ; Malic acid ; Mass spectrometry ; Mass spectroscopy ; Nucleic Acid Conformation ; Nucleosides ; Patients ; Ribonucleic acid ; RNA ; Spectroscopy ; Tandem Mass Spectrometry ; Urine</subject><ispartof>Analytica chimica acta, 2018-11, Vol.1034, p.110-118</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier BV Nov 30, 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c479t-b3c9ef8b953d5c0c2fa748c7a5b6596e4c403c7902133fc9d4503609fda294e63</citedby><cites>FETCH-LOGICAL-c479t-b3c9ef8b953d5c0c2fa748c7a5b6596e4c403c7902133fc9d4503609fda294e63</cites><orcidid>0000-0001-6194-1232</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30193624$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guo, Cheng</creatorcontrib><creatorcontrib>Xie, Cong</creatorcontrib><creatorcontrib>Chen, Qin</creatorcontrib><creatorcontrib>Cao, Xiaoji</creatorcontrib><creatorcontrib>Guo, Mengzhe</creatorcontrib><creatorcontrib>Zheng, Shu</creatorcontrib><creatorcontrib>Wang, Yinsheng</creatorcontrib><title>A novel malic acid-enhanced method for the analysis of 5-methyl-2′-deoxycytidine, 5-hydroxymethyl-2′-deoxycytidine, 5-methylcytidine and 5-hydroxymethylcytidine in human urine using hydrophilic interaction liquid chromatography-tandem mass spectrometry</title><title>Analytica chimica acta</title><addtitle>Anal Chim Acta</addtitle><description>5-Methyl-2′-deoxycytidine (5-mdC), 5-hydroxymethyl-2′-deoxycytidine (5-hmdC), 5-methylcytidine (5-mrC) and 5-hydroxymethylcytidine (5-hmrC) are epigenetic marks of DNA and RNA, and aberrant levels of these modified nucleosides were found to be associated with various cancers. Urine is a preferred source of biological fluid for biomarker discovery because the sample collection process is not invasive to patients. Herein, we developed a novel malic acid-enhanced hydrophilic interaction liquid chromatography-tandem mass spectrometry (HILIC-MS/MS) method for sensitive and simultaneous quantification of the modified cytosine nucleosides in human urine. Malic acid markedly increased the detection sensitivities of all four cytosine nucleosides, with the limits of detection (LODs) for 5-mdC, 5-hmdC, 5-mrC and 5-hmrC being 0.025, 0.025, 0.025 and 0.050 fmol, respectively. By using this method, we demonstrated, for the first time, the presence of 5-hmrC in human urine, and we successfully quantified 5-mdC, 5-hmdC, 5-mrC and 5-hmrC in urine samples collected from 90 patients with colorectal cancer (CRC) and 90 healthy controls. We found that the levels of 5-mdC, 5-hmdC, 5-mrC and 5-hmrC in urine were all substantially decreased in CRC patients, suggesting that these modified nucleosides might have great potential to be noninvasive biomarkers for early detection and prognosis of CRC. Together, we established a novel and sensitive method for detecting 5-methylated and 5-hydroxymethylated cytosine nucleosides in human urine and the results from this study may stimulate future investigations about the regulatory roles of these cytosine derivatives in the initiation and development of CRC. [Display omitted] •A novel method was reported for analysis of 5-methylated and 5-hydroxymethylated cytosine nucleosides in urine.•Enhancement of detection sensitivity was achieved with the assistance of malic acid.•Accurate quantification was realized by using stable isotope dilution method.•5-hydroxymethylcytidine was firstly discovered in human urine.•The modified cytosine nucleosides are present in significantly lower levels in urine of colorectal cancer patients.</description><subject>5-Methylated and 5-hydroxymethylated cytosine nucleosides</subject><subject>Biomarkers</subject><subject>Chromatography</subject><subject>Chromatography, Liquid</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Cytidine - analogs &amp; derivatives</subject><subject>Cytidine - chemistry</subject><subject>Cytidine - urine</subject><subject>Cytosine</subject><subject>Deoxycytidine - analogs &amp; derivatives</subject><subject>Deoxycytidine - chemistry</subject><subject>Deoxycytidine - urine</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA and RNA modification</subject><subject>Epigenetics</subject><subject>Human wastes</subject><subject>Humans</subject><subject>Hydrophilic interaction liquid chromatography-tandem mass spectrometry</subject><subject>Hydrophobic and Hydrophilic Interactions</subject><subject>Invasiveness</subject><subject>Liquid chromatography</subject><subject>Malates - chemistry</subject><subject>Malic acid</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Nucleic Acid Conformation</subject><subject>Nucleosides</subject><subject>Patients</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Spectroscopy</subject><subject>Tandem Mass Spectrometry</subject><subject>Urine</subject><issn>0003-2670</issn><issn>1873-4324</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9ks1u1DAUhQMC0aHwAGyQJTYsSLBjx0mEhFRV_EmV2MDa8tg3E48SO7WdEdnxTDwST4LDtCPooivr-nz3yL73ZNkLgguCCX-7L6SSRYlJU2Be4IY8zDakqWnOaMkeZRuMMc1LXuOz7GkI-1SWBLMn2RnFpKW8ZJsH2QWy7gADGuVgFJLK6BxsL60CjUaIvdOocx7FHpC0cliCCch1qMpXcRny8vfPX7kG92NRSzTaWHiTxH7RPl3dyxzF25vkru82njRjUT-P0qLZr-UcjN2hv-jUm_XdxkbwUkXjLBrM9Ww0Ur13o4xu5-XUL3lM_jCmb4aAwgQqJhWiX55ljzs5BHh-c55n3z9--Hb5Ob_6-unL5cVVrljdxnxLVQtds20rqiuFVdnJmjWqltWWVy0Hphimqm7ThCntVKtZhSnHbadl2TLg9Dx7f_Sd5u0IWoGNXg5i8maUfhFOGvG_Yk0vdu4gOOElZk0yeH1j4N31DCGK0QQFwyAtuDmItFpS8oZWLKGv7qB7N_u0vZWipKGkonWiyJFS3oXgoTs9hmCx5kvsRcqXWPMlMBcpX6nn5b-_OHXcBioB744ApFkeDHgRlIE1TcanoQvtzD32fwCWGOoJ</recordid><startdate>20181130</startdate><enddate>20181130</enddate><creator>Guo, Cheng</creator><creator>Xie, Cong</creator><creator>Chen, Qin</creator><creator>Cao, Xiaoji</creator><creator>Guo, Mengzhe</creator><creator>Zheng, Shu</creator><creator>Wang, Yinsheng</creator><general>Elsevier B.V</general><general>Elsevier BV</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>7QF</scope><scope>7QO</scope><scope>7QP</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7TK</scope><scope>7TM</scope><scope>7U5</scope><scope>7U7</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6194-1232</orcidid></search><sort><creationdate>20181130</creationdate><title>A novel malic acid-enhanced method for the analysis of 5-methyl-2′-deoxycytidine, 5-hydroxymethyl-2′-deoxycytidine, 5-methylcytidine and 5-hydroxymethylcytidine in human urine using hydrophilic interaction liquid chromatography-tandem mass spectrometry</title><author>Guo, Cheng ; Xie, Cong ; Chen, Qin ; Cao, Xiaoji ; Guo, Mengzhe ; Zheng, Shu ; Wang, Yinsheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c479t-b3c9ef8b953d5c0c2fa748c7a5b6596e4c403c7902133fc9d4503609fda294e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>5-Methylated and 5-hydroxymethylated cytosine nucleosides</topic><topic>Biomarkers</topic><topic>Chromatography</topic><topic>Chromatography, Liquid</topic><topic>Colorectal cancer</topic><topic>Colorectal carcinoma</topic><topic>Cytidine - analogs &amp; derivatives</topic><topic>Cytidine - chemistry</topic><topic>Cytidine - urine</topic><topic>Cytosine</topic><topic>Deoxycytidine - analogs &amp; derivatives</topic><topic>Deoxycytidine - chemistry</topic><topic>Deoxycytidine - urine</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA and RNA modification</topic><topic>Epigenetics</topic><topic>Human wastes</topic><topic>Humans</topic><topic>Hydrophilic interaction liquid chromatography-tandem mass spectrometry</topic><topic>Hydrophobic and Hydrophilic Interactions</topic><topic>Invasiveness</topic><topic>Liquid chromatography</topic><topic>Malates - chemistry</topic><topic>Malic acid</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Nucleic Acid Conformation</topic><topic>Nucleosides</topic><topic>Patients</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>Spectroscopy</topic><topic>Tandem Mass Spectrometry</topic><topic>Urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guo, Cheng</creatorcontrib><creatorcontrib>Xie, Cong</creatorcontrib><creatorcontrib>Chen, Qin</creatorcontrib><creatorcontrib>Cao, Xiaoji</creatorcontrib><creatorcontrib>Guo, Mengzhe</creatorcontrib><creatorcontrib>Zheng, Shu</creatorcontrib><creatorcontrib>Wang, Yinsheng</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics &amp; Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical &amp; Transportation Engineering Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology &amp; Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts – Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Analytica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guo, Cheng</au><au>Xie, Cong</au><au>Chen, Qin</au><au>Cao, Xiaoji</au><au>Guo, Mengzhe</au><au>Zheng, Shu</au><au>Wang, Yinsheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A novel malic acid-enhanced method for the analysis of 5-methyl-2′-deoxycytidine, 5-hydroxymethyl-2′-deoxycytidine, 5-methylcytidine and 5-hydroxymethylcytidine in human urine using hydrophilic interaction liquid chromatography-tandem mass spectrometry</atitle><jtitle>Analytica chimica acta</jtitle><addtitle>Anal Chim Acta</addtitle><date>2018-11-30</date><risdate>2018</risdate><volume>1034</volume><spage>110</spage><epage>118</epage><pages>110-118</pages><issn>0003-2670</issn><eissn>1873-4324</eissn><abstract>5-Methyl-2′-deoxycytidine (5-mdC), 5-hydroxymethyl-2′-deoxycytidine (5-hmdC), 5-methylcytidine (5-mrC) and 5-hydroxymethylcytidine (5-hmrC) are epigenetic marks of DNA and RNA, and aberrant levels of these modified nucleosides were found to be associated with various cancers. Urine is a preferred source of biological fluid for biomarker discovery because the sample collection process is not invasive to patients. Herein, we developed a novel malic acid-enhanced hydrophilic interaction liquid chromatography-tandem mass spectrometry (HILIC-MS/MS) method for sensitive and simultaneous quantification of the modified cytosine nucleosides in human urine. Malic acid markedly increased the detection sensitivities of all four cytosine nucleosides, with the limits of detection (LODs) for 5-mdC, 5-hmdC, 5-mrC and 5-hmrC being 0.025, 0.025, 0.025 and 0.050 fmol, respectively. By using this method, we demonstrated, for the first time, the presence of 5-hmrC in human urine, and we successfully quantified 5-mdC, 5-hmdC, 5-mrC and 5-hmrC in urine samples collected from 90 patients with colorectal cancer (CRC) and 90 healthy controls. We found that the levels of 5-mdC, 5-hmdC, 5-mrC and 5-hmrC in urine were all substantially decreased in CRC patients, suggesting that these modified nucleosides might have great potential to be noninvasive biomarkers for early detection and prognosis of CRC. Together, we established a novel and sensitive method for detecting 5-methylated and 5-hydroxymethylated cytosine nucleosides in human urine and the results from this study may stimulate future investigations about the regulatory roles of these cytosine derivatives in the initiation and development of CRC. [Display omitted] •A novel method was reported for analysis of 5-methylated and 5-hydroxymethylated cytosine nucleosides in urine.•Enhancement of detection sensitivity was achieved with the assistance of malic acid.•Accurate quantification was realized by using stable isotope dilution method.•5-hydroxymethylcytidine was firstly discovered in human urine.•The modified cytosine nucleosides are present in significantly lower levels in urine of colorectal cancer patients.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30193624</pmid><doi>10.1016/j.aca.2018.06.081</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-6194-1232</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0003-2670
ispartof Analytica chimica acta, 2018-11, Vol.1034, p.110-118
issn 0003-2670
1873-4324
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6162048
source ScienceDirect Journals
subjects 5-Methylated and 5-hydroxymethylated cytosine nucleosides
Biomarkers
Chromatography
Chromatography, Liquid
Colorectal cancer
Colorectal carcinoma
Cytidine - analogs & derivatives
Cytidine - chemistry
Cytidine - urine
Cytosine
Deoxycytidine - analogs & derivatives
Deoxycytidine - chemistry
Deoxycytidine - urine
Deoxyribonucleic acid
DNA
DNA and RNA modification
Epigenetics
Human wastes
Humans
Hydrophilic interaction liquid chromatography-tandem mass spectrometry
Hydrophobic and Hydrophilic Interactions
Invasiveness
Liquid chromatography
Malates - chemistry
Malic acid
Mass spectrometry
Mass spectroscopy
Nucleic Acid Conformation
Nucleosides
Patients
Ribonucleic acid
RNA
Spectroscopy
Tandem Mass Spectrometry
Urine
title A novel malic acid-enhanced method for the analysis of 5-methyl-2′-deoxycytidine, 5-hydroxymethyl-2′-deoxycytidine, 5-methylcytidine and 5-hydroxymethylcytidine in human urine using hydrophilic interaction liquid chromatography-tandem mass spectrometry
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T06%3A34%3A11IST&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=A%20novel%20malic%20acid-enhanced%20method%20for%20the%20analysis%20of%205-methyl-2%E2%80%B2-deoxycytidine,%205-hydroxymethyl-2%E2%80%B2-deoxycytidine,%205-methylcytidine%20and%205-hydroxymethylcytidine%20in%20human%20urine%20using%20hydrophilic%20interaction%20liquid%20chromatography-tandem%20mass%20spectrometry&rft.jtitle=Analytica%20chimica%20acta&rft.au=Guo,%20Cheng&rft.date=2018-11-30&rft.volume=1034&rft.spage=110&rft.epage=118&rft.pages=110-118&rft.issn=0003-2670&rft.eissn=1873-4324&rft_id=info:doi/10.1016/j.aca.2018.06.081&rft_dat=%3Cproquest_pubme%3E2131831537%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c479t-b3c9ef8b953d5c0c2fa748c7a5b6596e4c403c7902133fc9d4503609fda294e63%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2131831537&rft_id=info:pmid/30193624&rfr_iscdi=true