Comprehensive Evaluation of Serum tRF-17-WS7K092 as a Promising Biomarker for the Diagnosis of Gastric Cancer
Background. Gastric cancer (GC) is a malignant tumor of the gastrointestinal system. Since the early symptoms of GC are not obvious and lack efficient diagnostic markers, it is urgent to find new diagnostic markers with good sensitivity and specificity. tRNA-derived small RNAs (tsRNAs) are an emergi...
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description | Background. Gastric cancer (GC) is a malignant tumor of the gastrointestinal system. Since the early symptoms of GC are not obvious and lack efficient diagnostic markers, it is urgent to find new diagnostic markers with good sensitivity and specificity. tRNA-derived small RNAs (tsRNAs) are an emerging class of small noncoding RNAs with good abundance in body fluids. We aim to find new tsRNAs as biomarkers for GC diagnosis. Methods. High-throughput sequencing was used to identify differentially expressed tsRNAs in GC tissues, and quantitative real-time PCR was used to detect the expression level of tRF-17-WS7K092. Agarose gel electrophoresis and Sanger sequencing were performed to verify the characteristics of tRF-17-WS7K092. The diagnostic efficacy of tRF-17-WS7K092 was analyzed by the receiver operating characteristic curve. Results. In this study, the expression levels of tRF-17-WS7K092 were significantly increased in GC tissues, cells, and serum. After GC surgery, the expression level of serum tRF-17-WS7K092 decreased, and its high expression was associated with low survival rates. In addition, the expression level of serum tRF-17-WS7K092 was correlated with the T stage, TNM stage, lymph node metastasis, and nerve/vascular invasion and could distinguish GC patients from gastritis patients and healthy donors as well. Conclusions. The expression of serum tRF-17-WS7K092 was significantly increased in GC and decreased after GC surgery, suggesting that serum tRF-17-WS7K092 may serve as a promising biomarker for the diagnostic and prognostic monitoring of GC. |
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fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9553536</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A720580843</galeid><sourcerecordid>A720580843</sourcerecordid><originalsourceid>FETCH-LOGICAL-c453t-86d6da309e47f219f5635ad17fae5a3316a87eea9908109f82f20b937ed19b783</originalsourceid><addsrcrecordid>eNp90V2L1DAUBuAiCq6rd_6AgDeC1s1HkyY3wjruruKC4ipehjPtyUzWNhmTdsR_b8oMfl14lUAe3pzDW1WPGX3BmJRnnHJ-phuhW67uVCdM6bbWjaR3_7jfrx7kfEupaqhRJ9W4iuMu4RZD9nskF3sYZph8DCQ6coNpHsn08bJmbf3lpn1HDSeQCZAPKY4--7Ahr3wcIX3FRFxMZNoiee1hE2L2eYm4gjwl35EVhA7Tw-qegyHjo-N5Wn2-vPi0elNfv796uzq_rrtGiqnWqlc9CGqwaR1nxkklJPSsdYAShGAKdIsIxlDNqHGaO07XRrTYM7NutTitXh5yd_N6xL7DMCUY7C75MusPG8Hbv1-C39pN3FsjpZBClYCnx4AUv82YJ1vW7XAYIGCcs-Utl02jmBKFPvmH3sY5hbLeoiiX1Gj-W21gQOuDi-Xfbgm150VJTUtvRT0_qC7FnBO6XyMzapeK7VKxPVZc-LMD3_rQw3f_f_0TaOujug</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2720250982</pqid></control><display><type>article</type><title>Comprehensive Evaluation of Serum tRF-17-WS7K092 as a Promising Biomarker for the Diagnosis of Gastric Cancer</title><source>PubMed Central Open Access</source><source>Wiley Online Library Open Access</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Gu, Xinliang ; Zhang, Yu ; Huang, Yuejiao ; Ju, Shaoqing</creator><contributor>Mei, Jie ; Jie Mei</contributor><creatorcontrib>Gu, Xinliang ; Zhang, Yu ; Huang, Yuejiao ; Ju, Shaoqing ; Mei, Jie ; Jie Mei</creatorcontrib><description>Background. Gastric cancer (GC) is a malignant tumor of the gastrointestinal system. Since the early symptoms of GC are not obvious and lack efficient diagnostic markers, it is urgent to find new diagnostic markers with good sensitivity and specificity. tRNA-derived small RNAs (tsRNAs) are an emerging class of small noncoding RNAs with good abundance in body fluids. We aim to find new tsRNAs as biomarkers for GC diagnosis. Methods. High-throughput sequencing was used to identify differentially expressed tsRNAs in GC tissues, and quantitative real-time PCR was used to detect the expression level of tRF-17-WS7K092. Agarose gel electrophoresis and Sanger sequencing were performed to verify the characteristics of tRF-17-WS7K092. The diagnostic efficacy of tRF-17-WS7K092 was analyzed by the receiver operating characteristic curve. Results. In this study, the expression levels of tRF-17-WS7K092 were significantly increased in GC tissues, cells, and serum. After GC surgery, the expression level of serum tRF-17-WS7K092 decreased, and its high expression was associated with low survival rates. In addition, the expression level of serum tRF-17-WS7K092 was correlated with the T stage, TNM stage, lymph node metastasis, and nerve/vascular invasion and could distinguish GC patients from gastritis patients and healthy donors as well. Conclusions. The expression of serum tRF-17-WS7K092 was significantly increased in GC and decreased after GC surgery, suggesting that serum tRF-17-WS7K092 may serve as a promising biomarker for the diagnostic and prognostic monitoring of GC.</description><identifier>ISSN: 1687-8450</identifier><identifier>EISSN: 1687-8450</identifier><identifier>DOI: 10.1155/2022/8438726</identifier><language>eng</language><publisher>New York: Hindawi</publisher><subject>Analysis ; Antigens ; Biomarkers ; Cancer ; Cell cycle ; Clinical medicine ; Diagnosis ; DNA sequencing ; Gastric cancer ; Gastrointestinal system ; Gene expression ; Medical diagnosis ; Nucleotide sequencing ; Stomach cancer ; Transfer RNA ; Variance analysis</subject><ispartof>Journal of oncology, 2022-09, Vol.2022, p.1-12</ispartof><rights>Copyright © 2022 Xinliang Gu et al.</rights><rights>COPYRIGHT 2022 John Wiley & Sons, Inc.</rights><rights>Copyright © 2022 Xinliang Gu et al. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2022 Xinliang Gu et al. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c453t-86d6da309e47f219f5635ad17fae5a3316a87eea9908109f82f20b937ed19b783</citedby><cites>FETCH-LOGICAL-c453t-86d6da309e47f219f5635ad17fae5a3316a87eea9908109f82f20b937ed19b783</cites><orcidid>0000-0001-7448-2020</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/PMC9553536/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9553536/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids></links><search><contributor>Mei, Jie</contributor><contributor>Jie Mei</contributor><creatorcontrib>Gu, Xinliang</creatorcontrib><creatorcontrib>Zhang, Yu</creatorcontrib><creatorcontrib>Huang, Yuejiao</creatorcontrib><creatorcontrib>Ju, Shaoqing</creatorcontrib><title>Comprehensive Evaluation of Serum tRF-17-WS7K092 as a Promising Biomarker for the Diagnosis of Gastric Cancer</title><title>Journal of oncology</title><description>Background. Gastric cancer (GC) is a malignant tumor of the gastrointestinal system. Since the early symptoms of GC are not obvious and lack efficient diagnostic markers, it is urgent to find new diagnostic markers with good sensitivity and specificity. tRNA-derived small RNAs (tsRNAs) are an emerging class of small noncoding RNAs with good abundance in body fluids. We aim to find new tsRNAs as biomarkers for GC diagnosis. Methods. High-throughput sequencing was used to identify differentially expressed tsRNAs in GC tissues, and quantitative real-time PCR was used to detect the expression level of tRF-17-WS7K092. Agarose gel electrophoresis and Sanger sequencing were performed to verify the characteristics of tRF-17-WS7K092. The diagnostic efficacy of tRF-17-WS7K092 was analyzed by the receiver operating characteristic curve. Results. In this study, the expression levels of tRF-17-WS7K092 were significantly increased in GC tissues, cells, and serum. After GC surgery, the expression level of serum tRF-17-WS7K092 decreased, and its high expression was associated with low survival rates. In addition, the expression level of serum tRF-17-WS7K092 was correlated with the T stage, TNM stage, lymph node metastasis, and nerve/vascular invasion and could distinguish GC patients from gastritis patients and healthy donors as well. Conclusions. The expression of serum tRF-17-WS7K092 was significantly increased in GC and decreased after GC surgery, suggesting that serum tRF-17-WS7K092 may serve as a promising biomarker for the diagnostic and prognostic monitoring of GC.</description><subject>Analysis</subject><subject>Antigens</subject><subject>Biomarkers</subject><subject>Cancer</subject><subject>Cell cycle</subject><subject>Clinical medicine</subject><subject>Diagnosis</subject><subject>DNA sequencing</subject><subject>Gastric cancer</subject><subject>Gastrointestinal system</subject><subject>Gene expression</subject><subject>Medical diagnosis</subject><subject>Nucleotide sequencing</subject><subject>Stomach cancer</subject><subject>Transfer RNA</subject><subject>Variance analysis</subject><issn>1687-8450</issn><issn>1687-8450</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp90V2L1DAUBuAiCq6rd_6AgDeC1s1HkyY3wjruruKC4ipehjPtyUzWNhmTdsR_b8oMfl14lUAe3pzDW1WPGX3BmJRnnHJ-phuhW67uVCdM6bbWjaR3_7jfrx7kfEupaqhRJ9W4iuMu4RZD9nskF3sYZph8DCQ6coNpHsn08bJmbf3lpn1HDSeQCZAPKY4--7Ahr3wcIX3FRFxMZNoiee1hE2L2eYm4gjwl35EVhA7Tw-qegyHjo-N5Wn2-vPi0elNfv796uzq_rrtGiqnWqlc9CGqwaR1nxkklJPSsdYAShGAKdIsIxlDNqHGaO07XRrTYM7NutTitXh5yd_N6xL7DMCUY7C75MusPG8Hbv1-C39pN3FsjpZBClYCnx4AUv82YJ1vW7XAYIGCcs-Utl02jmBKFPvmH3sY5hbLeoiiX1Gj-W21gQOuDi-Xfbgm150VJTUtvRT0_qC7FnBO6XyMzapeK7VKxPVZc-LMD3_rQw3f_f_0TaOujug</recordid><startdate>20220919</startdate><enddate>20220919</enddate><creator>Gu, Xinliang</creator><creator>Zhang, Yu</creator><creator>Huang, Yuejiao</creator><creator>Ju, Shaoqing</creator><general>Hindawi</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7448-2020</orcidid></search><sort><creationdate>20220919</creationdate><title>Comprehensive Evaluation of Serum tRF-17-WS7K092 as a Promising Biomarker for the Diagnosis of Gastric Cancer</title><author>Gu, Xinliang ; Zhang, Yu ; Huang, Yuejiao ; Ju, Shaoqing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c453t-86d6da309e47f219f5635ad17fae5a3316a87eea9908109f82f20b937ed19b783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Analysis</topic><topic>Antigens</topic><topic>Biomarkers</topic><topic>Cancer</topic><topic>Cell cycle</topic><topic>Clinical medicine</topic><topic>Diagnosis</topic><topic>DNA sequencing</topic><topic>Gastric cancer</topic><topic>Gastrointestinal system</topic><topic>Gene expression</topic><topic>Medical diagnosis</topic><topic>Nucleotide sequencing</topic><topic>Stomach cancer</topic><topic>Transfer RNA</topic><topic>Variance analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gu, Xinliang</creatorcontrib><creatorcontrib>Zhang, Yu</creatorcontrib><creatorcontrib>Huang, Yuejiao</creatorcontrib><creatorcontrib>Ju, Shaoqing</creatorcontrib><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Nursing & Allied Health Premium</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gu, Xinliang</au><au>Zhang, Yu</au><au>Huang, Yuejiao</au><au>Ju, Shaoqing</au><au>Mei, Jie</au><au>Jie Mei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comprehensive Evaluation of Serum tRF-17-WS7K092 as a Promising Biomarker for the Diagnosis of Gastric Cancer</atitle><jtitle>Journal of oncology</jtitle><date>2022-09-19</date><risdate>2022</risdate><volume>2022</volume><spage>1</spage><epage>12</epage><pages>1-12</pages><issn>1687-8450</issn><eissn>1687-8450</eissn><abstract>Background. Gastric cancer (GC) is a malignant tumor of the gastrointestinal system. Since the early symptoms of GC are not obvious and lack efficient diagnostic markers, it is urgent to find new diagnostic markers with good sensitivity and specificity. tRNA-derived small RNAs (tsRNAs) are an emerging class of small noncoding RNAs with good abundance in body fluids. We aim to find new tsRNAs as biomarkers for GC diagnosis. Methods. High-throughput sequencing was used to identify differentially expressed tsRNAs in GC tissues, and quantitative real-time PCR was used to detect the expression level of tRF-17-WS7K092. Agarose gel electrophoresis and Sanger sequencing were performed to verify the characteristics of tRF-17-WS7K092. The diagnostic efficacy of tRF-17-WS7K092 was analyzed by the receiver operating characteristic curve. Results. In this study, the expression levels of tRF-17-WS7K092 were significantly increased in GC tissues, cells, and serum. After GC surgery, the expression level of serum tRF-17-WS7K092 decreased, and its high expression was associated with low survival rates. In addition, the expression level of serum tRF-17-WS7K092 was correlated with the T stage, TNM stage, lymph node metastasis, and nerve/vascular invasion and could distinguish GC patients from gastritis patients and healthy donors as well. Conclusions. The expression of serum tRF-17-WS7K092 was significantly increased in GC and decreased after GC surgery, suggesting that serum tRF-17-WS7K092 may serve as a promising biomarker for the diagnostic and prognostic monitoring of GC.</abstract><cop>New York</cop><pub>Hindawi</pub><doi>10.1155/2022/8438726</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-7448-2020</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Antigens Biomarkers Cancer Cell cycle Clinical medicine Diagnosis DNA sequencing Gastric cancer Gastrointestinal system Gene expression Medical diagnosis Nucleotide sequencing Stomach cancer Transfer RNA Variance analysis |
title | Comprehensive Evaluation of Serum tRF-17-WS7K092 as a Promising Biomarker for the Diagnosis of Gastric Cancer |
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