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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...
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Published in: | Analytica chimica acta 2018-11, Vol.1034, p.110-118 |
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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 |
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[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 & 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</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 & derivatives</subject><subject>Cytidine - chemistry</subject><subject>Cytidine - urine</subject><subject>Cytosine</subject><subject>Deoxycytidine - analogs & 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 & derivatives</topic><topic>Cytidine - chemistry</topic><topic>Cytidine - urine</topic><topic>Cytosine</topic><topic>Deoxycytidine - analogs & 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 & Calcified Tissue Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical & 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 & 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> |
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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 |
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