Bioinformatics identification of potentially involved microRNAs in Tibetan with gastric cancer based on microRNA profiling
The incidence of gastric cancer is high in Chinese Tibetan. This study aimed to identify the differentially expressed microRNAs (miRNAs) and further explore their potential roles in Tibetan with gastric cancer so as to predict potential therapeutic targets. A total of 10 Tibetan patients (male:femal...
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Veröffentlicht in: | Cancer Cell International 2015-12, Vol.15 (1), p.115-115, Article 115 |
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description | The incidence of gastric cancer is high in Chinese Tibetan. This study aimed to identify the differentially expressed microRNAs (miRNAs) and further explore their potential roles in Tibetan with gastric cancer so as to predict potential therapeutic targets.
A total of 10 Tibetan patients (male:female = 6:4) with gastric cancer were enrolled for isolation of matched gastric cancer and adjacent non-cancerous tissue samples. Affymetrix GeneChip microRNA 3.0 Array was employed for detection of miRNA expression in samples. Differential expression analysis between two sample groups was analyzed using Limma package. Then, MultiMiR package was used to predict targets for miRNAs. Following, the target genes were put into DAVID (Database for Annotation, Visualization and Integrated Discovery) to identify the significant pathways of miRNAs.
Using Limma package in R, a total of 27 differentially expressed miRNAs were screened out in gastric cancer, including 25 down-regulated (e.g. hsa-miR-148a-3p, hsa-miR-148b-3p and hsa-miR-363-3p) and 2 up-regulated miRNAs. According to multiMiR package, a number of 1445 target genes (e.g. Wnt1, KLF4 and S1PR1) of 13 differentially expressed miRNAs were screened out. Among those miRNAs, hsa-miR-148a-3p, hsa-miR-148b-3p and hsa-miR-363-3p were identified with the most target genes. Furthermore, three miRNAs were significantly enriched in numerous common cancer-related pathways, including "Wnt signaling pathway", "MAPK signaling pathway" and "Jak-STAT signaling pathway".
The present study identified a downregulation and enrichment in cancer-related pathways of hsa-miR-148a-3p, hsa-miR-148b-3p and hsa-miR-363-3p in Tibetan with gastric cancer, which can be suggested as therapeutic targets. |
doi_str_mv | 10.1186/s12935-015-0266-1 |
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A total of 10 Tibetan patients (male:female = 6:4) with gastric cancer were enrolled for isolation of matched gastric cancer and adjacent non-cancerous tissue samples. Affymetrix GeneChip microRNA 3.0 Array was employed for detection of miRNA expression in samples. Differential expression analysis between two sample groups was analyzed using Limma package. Then, MultiMiR package was used to predict targets for miRNAs. Following, the target genes were put into DAVID (Database for Annotation, Visualization and Integrated Discovery) to identify the significant pathways of miRNAs.
Using Limma package in R, a total of 27 differentially expressed miRNAs were screened out in gastric cancer, including 25 down-regulated (e.g. hsa-miR-148a-3p, hsa-miR-148b-3p and hsa-miR-363-3p) and 2 up-regulated miRNAs. According to multiMiR package, a number of 1445 target genes (e.g. Wnt1, KLF4 and S1PR1) of 13 differentially expressed miRNAs were screened out. Among those miRNAs, hsa-miR-148a-3p, hsa-miR-148b-3p and hsa-miR-363-3p were identified with the most target genes. Furthermore, three miRNAs were significantly enriched in numerous common cancer-related pathways, including "Wnt signaling pathway", "MAPK signaling pathway" and "Jak-STAT signaling pathway".
The present study identified a downregulation and enrichment in cancer-related pathways of hsa-miR-148a-3p, hsa-miR-148b-3p and hsa-miR-363-3p in Tibetan with gastric cancer, which can be suggested as therapeutic targets.</description><identifier>ISSN: 1475-2867</identifier><identifier>EISSN: 1475-2867</identifier><identifier>DOI: 10.1186/s12935-015-0266-1</identifier><identifier>PMID: 26692821</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Analysis ; Bioinformatics ; Cancer ; Development and progression ; Health aspects ; Medical research ; Medicine, Experimental ; MicroRNA ; Primary Research ; Stomach cancer</subject><ispartof>Cancer Cell International, 2015-12, Vol.15 (1), p.115-115, Article 115</ispartof><rights>COPYRIGHT 2015 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2015</rights><rights>Luo et al. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c598t-1ce5061ba9192eb3334bb44d2e036e86cdcd7a6cf03eed550fbc7212a01dd5ea3</citedby><cites>FETCH-LOGICAL-c598t-1ce5061ba9192eb3334bb44d2e036e86cdcd7a6cf03eed550fbc7212a01dd5ea3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676900/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676900/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26692821$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Luo, Yushuang</creatorcontrib><creatorcontrib>Zhang, Chengwu</creatorcontrib><creatorcontrib>Tang, Feng</creatorcontrib><creatorcontrib>Zhao, Junhui</creatorcontrib><creatorcontrib>Shen, Cunfang</creatorcontrib><creatorcontrib>Wang, Cheng</creatorcontrib><creatorcontrib>Yu, Pengjie</creatorcontrib><creatorcontrib>Wang, Miaozhou</creatorcontrib><creatorcontrib>Li, Yan</creatorcontrib><creatorcontrib>Di, J I</creatorcontrib><creatorcontrib>Chen, Rong</creatorcontrib><creatorcontrib>Rili, Ge</creatorcontrib><title>Bioinformatics identification of potentially involved microRNAs in Tibetan with gastric cancer based on microRNA profiling</title><title>Cancer Cell International</title><addtitle>Cancer Cell Int</addtitle><description>The incidence of gastric cancer is high in Chinese Tibetan. This study aimed to identify the differentially expressed microRNAs (miRNAs) and further explore their potential roles in Tibetan with gastric cancer so as to predict potential therapeutic targets.
A total of 10 Tibetan patients (male:female = 6:4) with gastric cancer were enrolled for isolation of matched gastric cancer and adjacent non-cancerous tissue samples. Affymetrix GeneChip microRNA 3.0 Array was employed for detection of miRNA expression in samples. Differential expression analysis between two sample groups was analyzed using Limma package. Then, MultiMiR package was used to predict targets for miRNAs. Following, the target genes were put into DAVID (Database for Annotation, Visualization and Integrated Discovery) to identify the significant pathways of miRNAs.
Using Limma package in R, a total of 27 differentially expressed miRNAs were screened out in gastric cancer, including 25 down-regulated (e.g. hsa-miR-148a-3p, hsa-miR-148b-3p and hsa-miR-363-3p) and 2 up-regulated miRNAs. According to multiMiR package, a number of 1445 target genes (e.g. Wnt1, KLF4 and S1PR1) of 13 differentially expressed miRNAs were screened out. Among those miRNAs, hsa-miR-148a-3p, hsa-miR-148b-3p and hsa-miR-363-3p were identified with the most target genes. Furthermore, three miRNAs were significantly enriched in numerous common cancer-related pathways, including "Wnt signaling pathway", "MAPK signaling pathway" and "Jak-STAT signaling pathway".
The present study identified a downregulation and enrichment in cancer-related pathways of hsa-miR-148a-3p, hsa-miR-148b-3p and hsa-miR-363-3p in Tibetan with gastric cancer, which can be suggested as therapeutic targets.</description><subject>Analysis</subject><subject>Bioinformatics</subject><subject>Cancer</subject><subject>Development and progression</subject><subject>Health aspects</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>MicroRNA</subject><subject>Primary Research</subject><subject>Stomach cancer</subject><issn>1475-2867</issn><issn>1475-2867</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpdUl1rFDEUDaLYWv0BvkjAF1-m5mYmmZkXYS31A4qC1OeQSe5sU2aSNZldqb--d922VAkhX-ec5J4cxl6DOAXo9PsCsq9VJYC61LqCJ-wYmlZVstPt00fzI_ailGshoO20eM6OCNzLTsIx-_MxpBDHlGe7BFd48BiXMAZHyxR5GvkmLfstO003PMRdmnbo-RxcTj--rYgQ-WUYcLGR_w7LFV_bsuTguLPRYeaDLQQnpXsG3-Q0hinE9Uv2bLRTwVd34wn7-en88uxLdfH989ez1UXlVN8tFThUQsNge-glDnVdN8PQNF6iqDV22nnnW6vdKGpEr5QYB9dKkFaA9wptfcI-HHQ322FG76iabCezyWG2-cYkG8y_JzFcmXXamUa3uheCBN7dCeT0a4tlMXMoDqfJRkzbYqBV0HRK_oW-_Q96nbY5UnmEanst6L80oU4PqLWd0Oztp3sdNY9kU4pIBqFZNbrrG92rhghwIJCHpWQcH14PwuyjYA5RMBQFs4-CAeK8eVz2A-P-7-tb672yNA</recordid><startdate>20151212</startdate><enddate>20151212</enddate><creator>Luo, Yushuang</creator><creator>Zhang, Chengwu</creator><creator>Tang, Feng</creator><creator>Zhao, Junhui</creator><creator>Shen, Cunfang</creator><creator>Wang, Cheng</creator><creator>Yu, Pengjie</creator><creator>Wang, Miaozhou</creator><creator>Li, Yan</creator><creator>Di, J I</creator><creator>Chen, Rong</creator><creator>Rili, Ge</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IAO</scope><scope>3V.</scope><scope>7TM</scope><scope>7TO</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>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151212</creationdate><title>Bioinformatics identification of potentially involved microRNAs in Tibetan with gastric cancer based on microRNA profiling</title><author>Luo, Yushuang ; Zhang, Chengwu ; Tang, Feng ; Zhao, Junhui ; Shen, Cunfang ; Wang, Cheng ; Yu, Pengjie ; Wang, Miaozhou ; Li, Yan ; Di, J I ; Chen, Rong ; Rili, Ge</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c598t-1ce5061ba9192eb3334bb44d2e036e86cdcd7a6cf03eed550fbc7212a01dd5ea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Analysis</topic><topic>Bioinformatics</topic><topic>Cancer</topic><topic>Development and progression</topic><topic>Health aspects</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>MicroRNA</topic><topic>Primary Research</topic><topic>Stomach cancer</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luo, Yushuang</creatorcontrib><creatorcontrib>Zhang, Chengwu</creatorcontrib><creatorcontrib>Tang, Feng</creatorcontrib><creatorcontrib>Zhao, Junhui</creatorcontrib><creatorcontrib>Shen, Cunfang</creatorcontrib><creatorcontrib>Wang, Cheng</creatorcontrib><creatorcontrib>Yu, Pengjie</creatorcontrib><creatorcontrib>Wang, Miaozhou</creatorcontrib><creatorcontrib>Li, Yan</creatorcontrib><creatorcontrib>Di, J I</creatorcontrib><creatorcontrib>Chen, Rong</creatorcontrib><creatorcontrib>Rili, Ge</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale Academic OneFile</collection><collection>ProQuest Central (Corporate)</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</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>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</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>Cancer Cell International</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luo, Yushuang</au><au>Zhang, Chengwu</au><au>Tang, Feng</au><au>Zhao, Junhui</au><au>Shen, Cunfang</au><au>Wang, Cheng</au><au>Yu, Pengjie</au><au>Wang, Miaozhou</au><au>Li, Yan</au><au>Di, J I</au><au>Chen, Rong</au><au>Rili, Ge</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bioinformatics identification of potentially involved microRNAs in Tibetan with gastric cancer based on microRNA profiling</atitle><jtitle>Cancer Cell International</jtitle><addtitle>Cancer Cell Int</addtitle><date>2015-12-12</date><risdate>2015</risdate><volume>15</volume><issue>1</issue><spage>115</spage><epage>115</epage><pages>115-115</pages><artnum>115</artnum><issn>1475-2867</issn><eissn>1475-2867</eissn><abstract>The incidence of gastric cancer is high in Chinese Tibetan. This study aimed to identify the differentially expressed microRNAs (miRNAs) and further explore their potential roles in Tibetan with gastric cancer so as to predict potential therapeutic targets.
A total of 10 Tibetan patients (male:female = 6:4) with gastric cancer were enrolled for isolation of matched gastric cancer and adjacent non-cancerous tissue samples. Affymetrix GeneChip microRNA 3.0 Array was employed for detection of miRNA expression in samples. Differential expression analysis between two sample groups was analyzed using Limma package. Then, MultiMiR package was used to predict targets for miRNAs. Following, the target genes were put into DAVID (Database for Annotation, Visualization and Integrated Discovery) to identify the significant pathways of miRNAs.
Using Limma package in R, a total of 27 differentially expressed miRNAs were screened out in gastric cancer, including 25 down-regulated (e.g. hsa-miR-148a-3p, hsa-miR-148b-3p and hsa-miR-363-3p) and 2 up-regulated miRNAs. According to multiMiR package, a number of 1445 target genes (e.g. Wnt1, KLF4 and S1PR1) of 13 differentially expressed miRNAs were screened out. Among those miRNAs, hsa-miR-148a-3p, hsa-miR-148b-3p and hsa-miR-363-3p were identified with the most target genes. Furthermore, three miRNAs were significantly enriched in numerous common cancer-related pathways, including "Wnt signaling pathway", "MAPK signaling pathway" and "Jak-STAT signaling pathway".
The present study identified a downregulation and enrichment in cancer-related pathways of hsa-miR-148a-3p, hsa-miR-148b-3p and hsa-miR-363-3p in Tibetan with gastric cancer, which can be suggested as therapeutic targets.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26692821</pmid><doi>10.1186/s12935-015-0266-1</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Bioinformatics Cancer Development and progression Health aspects Medical research Medicine, Experimental MicroRNA Primary Research Stomach cancer |
title | Bioinformatics identification of potentially involved microRNAs in Tibetan with gastric cancer based on microRNA profiling |
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