Expression of miR-520c in intestinal type gastric adenocarcinoma
MicroRNAs are small non-coding RNAs that participate in post-transcriptional gene regulation in cells thereby playing active role in pathological conditions and have been nominated as new class of biomarkers in disease including cancer. miR-520c has been reported as potential oncogenic micro-RNA in...
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Veröffentlicht in: | Journal of gastrointestinal oncology 2018-12, Vol.9 (6), p.1184-1189 |
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container_title | Journal of gastrointestinal oncology |
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creator | Azimzadeh-Isfanjani, Arash Safaralizadeh, Reza Hosseinpour-Feizi, Mohamadali Shokouhi, Behrouz Nemati, Masuomeh Moaddab, Seyyed-Yaghoub |
description | MicroRNAs are small non-coding RNAs that participate in post-transcriptional gene regulation in cells thereby playing active role in pathological conditions and have been nominated as new class of biomarkers in disease including cancer. miR-520c has been reported as potential oncogenic micro-RNA in several previous studies. Gastric cancer is the most common cancer of digestive tract and the fourth prevalent cancer worldwide with the intestinal-type gastric adenocarcinoma (IGA) the dominant type of gastric malignancies. This study aimed to explore miR-520c putative role, in IGA and patient's clinicopathological features.
Total RNA was first extracted from 42 pairs of IGA tissues and relevant non-tumorous adjacent tissues. cDNA was synthesized from extracted RNAs using specific primers for miR-520c. The level of miR-520c was quantified using SYBER Green Real-Time PCR master mix. The relationship between miR-520c expression and clinicopathological features were examined.
Our study resulted in no differential expression of miR-520c in IGA. There was no significant correlation between miR-520c expression and clinicopathological features including tumor grade, genus and age groups.
To our knowledge, this is the first report about exploring miR-520c expression in IGA tissue samples. Our results do not verify miR-520c previously established oncogenic role in IGA. |
doi_str_mv | 10.21037/jgo.2018.08.09 |
format | Article |
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Total RNA was first extracted from 42 pairs of IGA tissues and relevant non-tumorous adjacent tissues. cDNA was synthesized from extracted RNAs using specific primers for miR-520c. The level of miR-520c was quantified using SYBER Green Real-Time PCR master mix. The relationship between miR-520c expression and clinicopathological features were examined.
Our study resulted in no differential expression of miR-520c in IGA. There was no significant correlation between miR-520c expression and clinicopathological features including tumor grade, genus and age groups.
To our knowledge, this is the first report about exploring miR-520c expression in IGA tissue samples. Our results do not verify miR-520c previously established oncogenic role in IGA.</description><identifier>ISSN: 2078-6891</identifier><identifier>EISSN: 2219-679X</identifier><identifier>DOI: 10.21037/jgo.2018.08.09</identifier><identifier>PMID: 30603140</identifier><language>eng</language><publisher>China: AME Publishing Company</publisher><subject>Original</subject><ispartof>Journal of gastrointestinal oncology, 2018-12, Vol.9 (6), p.1184-1189</ispartof><rights>2018 Journal of Gastrointestinal Oncology. All rights reserved. 2018 Journal of Gastrointestinal Oncology.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-5c632aa6b9ff67bfeef88e4025bc054a67e93acd38ae291cc94ec89ede65287a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286939/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286939/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30603140$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Azimzadeh-Isfanjani, Arash</creatorcontrib><creatorcontrib>Safaralizadeh, Reza</creatorcontrib><creatorcontrib>Hosseinpour-Feizi, Mohamadali</creatorcontrib><creatorcontrib>Shokouhi, Behrouz</creatorcontrib><creatorcontrib>Nemati, Masuomeh</creatorcontrib><creatorcontrib>Moaddab, Seyyed-Yaghoub</creatorcontrib><title>Expression of miR-520c in intestinal type gastric adenocarcinoma</title><title>Journal of gastrointestinal oncology</title><addtitle>J Gastrointest Oncol</addtitle><description>MicroRNAs are small non-coding RNAs that participate in post-transcriptional gene regulation in cells thereby playing active role in pathological conditions and have been nominated as new class of biomarkers in disease including cancer. miR-520c has been reported as potential oncogenic micro-RNA in several previous studies. Gastric cancer is the most common cancer of digestive tract and the fourth prevalent cancer worldwide with the intestinal-type gastric adenocarcinoma (IGA) the dominant type of gastric malignancies. This study aimed to explore miR-520c putative role, in IGA and patient's clinicopathological features.
Total RNA was first extracted from 42 pairs of IGA tissues and relevant non-tumorous adjacent tissues. cDNA was synthesized from extracted RNAs using specific primers for miR-520c. The level of miR-520c was quantified using SYBER Green Real-Time PCR master mix. The relationship between miR-520c expression and clinicopathological features were examined.
Our study resulted in no differential expression of miR-520c in IGA. There was no significant correlation between miR-520c expression and clinicopathological features including tumor grade, genus and age groups.
To our knowledge, this is the first report about exploring miR-520c expression in IGA tissue samples. Our results do not verify miR-520c previously established oncogenic role in IGA.</description><subject>Original</subject><issn>2078-6891</issn><issn>2219-679X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpVUE1LxDAQDaKorJ69SY9euk6SNk0uoizrBwiCKHgLaTpds7TNmnRF_73RVdHhwQzM482bR8gRhSmjwKvT5cJPGVA5hQS1RfYZoyoXlXraTjNUMhdS0T1yGOMSUhWqhJLtkj0OAjgtYJ-cz99WAWN0fsh8m_XuPi8Z2MwNCSPG0Q2my8b3FWYLE8fgbGYaHLw1wbrB9-aA7LSmi3j43Sfk8XL-MLvOb--ubmYXt7nlio95aQVnxohata2o6haxlRILYGVtoSyMqFBxYxsuDTJFrVUFWqmwQVEyWRk-IWcb3dW67rGxOIzBdHoVXG_Cu_bG6f-bwT3rhX_VgkmhkocJOfkWCP5lnT7TvYsWu84M6NdRMyo40BIqnqinG6oNPsaA7e8ZCvorep2i15_Ra0j4FD_-6-6X_xM0_wAw44Dd</recordid><startdate>201812</startdate><enddate>201812</enddate><creator>Azimzadeh-Isfanjani, Arash</creator><creator>Safaralizadeh, Reza</creator><creator>Hosseinpour-Feizi, Mohamadali</creator><creator>Shokouhi, Behrouz</creator><creator>Nemati, Masuomeh</creator><creator>Moaddab, Seyyed-Yaghoub</creator><general>AME Publishing Company</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201812</creationdate><title>Expression of miR-520c in intestinal type gastric adenocarcinoma</title><author>Azimzadeh-Isfanjani, Arash ; Safaralizadeh, Reza ; Hosseinpour-Feizi, Mohamadali ; Shokouhi, Behrouz ; Nemati, Masuomeh ; Moaddab, Seyyed-Yaghoub</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-5c632aa6b9ff67bfeef88e4025bc054a67e93acd38ae291cc94ec89ede65287a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Original</topic><toplevel>online_resources</toplevel><creatorcontrib>Azimzadeh-Isfanjani, Arash</creatorcontrib><creatorcontrib>Safaralizadeh, Reza</creatorcontrib><creatorcontrib>Hosseinpour-Feizi, Mohamadali</creatorcontrib><creatorcontrib>Shokouhi, Behrouz</creatorcontrib><creatorcontrib>Nemati, Masuomeh</creatorcontrib><creatorcontrib>Moaddab, Seyyed-Yaghoub</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of gastrointestinal oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Azimzadeh-Isfanjani, Arash</au><au>Safaralizadeh, Reza</au><au>Hosseinpour-Feizi, Mohamadali</au><au>Shokouhi, Behrouz</au><au>Nemati, Masuomeh</au><au>Moaddab, Seyyed-Yaghoub</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of miR-520c in intestinal type gastric adenocarcinoma</atitle><jtitle>Journal of gastrointestinal oncology</jtitle><addtitle>J Gastrointest Oncol</addtitle><date>2018-12</date><risdate>2018</risdate><volume>9</volume><issue>6</issue><spage>1184</spage><epage>1189</epage><pages>1184-1189</pages><issn>2078-6891</issn><eissn>2219-679X</eissn><abstract>MicroRNAs are small non-coding RNAs that participate in post-transcriptional gene regulation in cells thereby playing active role in pathological conditions and have been nominated as new class of biomarkers in disease including cancer. miR-520c has been reported as potential oncogenic micro-RNA in several previous studies. Gastric cancer is the most common cancer of digestive tract and the fourth prevalent cancer worldwide with the intestinal-type gastric adenocarcinoma (IGA) the dominant type of gastric malignancies. This study aimed to explore miR-520c putative role, in IGA and patient's clinicopathological features.
Total RNA was first extracted from 42 pairs of IGA tissues and relevant non-tumorous adjacent tissues. cDNA was synthesized from extracted RNAs using specific primers for miR-520c. The level of miR-520c was quantified using SYBER Green Real-Time PCR master mix. The relationship between miR-520c expression and clinicopathological features were examined.
Our study resulted in no differential expression of miR-520c in IGA. There was no significant correlation between miR-520c expression and clinicopathological features including tumor grade, genus and age groups.
To our knowledge, this is the first report about exploring miR-520c expression in IGA tissue samples. Our results do not verify miR-520c previously established oncogenic role in IGA.</abstract><cop>China</cop><pub>AME Publishing Company</pub><pmid>30603140</pmid><doi>10.21037/jgo.2018.08.09</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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title | Expression of miR-520c in intestinal type gastric adenocarcinoma |
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