Changes in the Expression of Long Non-Coding RNA SDMGC and Its Target Gene, TRIM16, in Patients with Gastric Cancer

Purpose Gastric cancer (GC) has been identified worldwide as one of the most common cancer types with a high mortality rate. LncRNA SDMGC has been recognized as an oncogene with regulatory effects on its target gene, TRIM16, which is believed to play a tumor-suppressing role in various cancers. Both...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of gastrointestinal cancer 2023-03, Vol.54 (1), p.44-50
Hauptverfasser: Seifi Inallou, Mina, Safaralizadeh, Reza, Rajabi, Ali, Hosseinpourfeizi, Mohammadali, Haghi, Mehdi
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 50
container_issue 1
container_start_page 44
container_title Journal of gastrointestinal cancer
container_volume 54
creator Seifi Inallou, Mina
Safaralizadeh, Reza
Rajabi, Ali
Hosseinpourfeizi, Mohammadali
Haghi, Mehdi
description Purpose Gastric cancer (GC) has been identified worldwide as one of the most common cancer types with a high mortality rate. LncRNA SDMGC has been recognized as an oncogene with regulatory effects on its target gene, TRIM16, which is believed to play a tumor-suppressing role in various cancers. Both these genes are involved in GC development, tumorigenesis, invasion, and metastasis. The current study is aimed to investigate the association of SDMGC and TRIM16 with GC susceptibility and GC patients’ clinicopathological characteristics. Methods A total of 100 GC tissues and their corresponding adjacent non-tumor tissues were sampled. Total RNA was then isolated to measure SDMGC and TRIM16 expression levels using quantitative reverse transcriptase (qRT)-PCR. Statistical analyses including the Mann–Whitney U test and correlation tests were carried out using R v4.5. GraphPad Prism was also used to plot the receiver operating curve (ROC). Results The results demonstrated the significant overexpression of lncRNAs SDMGC and downregulation of TRIM16 in GC tissues as compared to their corresponding marginal normal tissue samples ( P  = 0.005 and P  = 0.009, respectively). No association with clinicopathological variables was observed for either SDMGC or TRIM16. Moreover, the results demonstrated a small positive correlation between SDMGC and TRIM16. Evaluation of the diagnostic value of SDMGC and TRIM16 showed poor biomarker potency for these genes. Conclusion In conclusion, the results indicated an increase in the expression of SDMGC and a decline in the expression pattern of TRIM16 among the Iranian population. The results indicated a key tumor-accelerative function of SDMGC and a pivotal tumor-suppressing role of TRIM16 in GC patients.
doi_str_mv 10.1007/s12029-021-00791-y
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2616288048</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2616288048</sourcerecordid><originalsourceid>FETCH-LOGICAL-c347t-e5f5fe3a8e51d2048abff175d02a272a58202f99e0fcfd54e79aafd8e1e78cba3</originalsourceid><addsrcrecordid>eNp9kE1PAjEQhhujEUT_gAfTowdW2-73kay4kgAaxHNTdqewBFpsd6P8e4uLHD3NTOaZN5kHoVtKHigh8aOljLDUI4x6bkyptz9DXZoG1IsiPzo_9SzpoCtr14REQUjpJer4QRonDuoim62EWoLFlcL1CvDwe2fA2korrCUea7XEU628TJeVa2fTAX5_muQZFqrEo9riuTBLqHEOCvp4PhtNaNQ_ZL2JugLlgK-qXuFc2NpUBc6EKsBcowspNhZujrWHPp6H8-zFG7_mo2ww9go_iGsPQhlK8EUCIS0ZCRKxkJLGYUmYYDETYeLel2kKRBayDAOIUyFkmQCFOCkWwu-h-zZ3Z_RnA7bm28oWsNkIBbqxnEXUuUlcskNZixZGW2tA8p2ptsLsOSX8IJu3srmTzX9l8707ujvmN4stlKeTP7sO8FvAupWzbPhaN0a5n_-L_QHJ9Yl_</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2616288048</pqid></control><display><type>article</type><title>Changes in the Expression of Long Non-Coding RNA SDMGC and Its Target Gene, TRIM16, in Patients with Gastric Cancer</title><source>MEDLINE</source><source>SpringerLink Journals</source><creator>Seifi Inallou, Mina ; Safaralizadeh, Reza ; Rajabi, Ali ; Hosseinpourfeizi, Mohammadali ; Haghi, Mehdi</creator><creatorcontrib>Seifi Inallou, Mina ; Safaralizadeh, Reza ; Rajabi, Ali ; Hosseinpourfeizi, Mohammadali ; Haghi, Mehdi</creatorcontrib><description>Purpose Gastric cancer (GC) has been identified worldwide as one of the most common cancer types with a high mortality rate. LncRNA SDMGC has been recognized as an oncogene with regulatory effects on its target gene, TRIM16, which is believed to play a tumor-suppressing role in various cancers. Both these genes are involved in GC development, tumorigenesis, invasion, and metastasis. The current study is aimed to investigate the association of SDMGC and TRIM16 with GC susceptibility and GC patients’ clinicopathological characteristics. Methods A total of 100 GC tissues and their corresponding adjacent non-tumor tissues were sampled. Total RNA was then isolated to measure SDMGC and TRIM16 expression levels using quantitative reverse transcriptase (qRT)-PCR. Statistical analyses including the Mann–Whitney U test and correlation tests were carried out using R v4.5. GraphPad Prism was also used to plot the receiver operating curve (ROC). Results The results demonstrated the significant overexpression of lncRNAs SDMGC and downregulation of TRIM16 in GC tissues as compared to their corresponding marginal normal tissue samples ( P  = 0.005 and P  = 0.009, respectively). No association with clinicopathological variables was observed for either SDMGC or TRIM16. Moreover, the results demonstrated a small positive correlation between SDMGC and TRIM16. Evaluation of the diagnostic value of SDMGC and TRIM16 showed poor biomarker potency for these genes. Conclusion In conclusion, the results indicated an increase in the expression of SDMGC and a decline in the expression pattern of TRIM16 among the Iranian population. The results indicated a key tumor-accelerative function of SDMGC and a pivotal tumor-suppressing role of TRIM16 in GC patients.</description><identifier>ISSN: 1941-6628</identifier><identifier>EISSN: 1941-6636</identifier><identifier>DOI: 10.1007/s12029-021-00791-y</identifier><identifier>PMID: 34978663</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Cancer Research ; Cell Line, Tumor ; Gastroenterology ; Gene Expression Regulation, Neoplastic ; Humans ; Internal Medicine ; Iran ; Medicine ; Medicine &amp; Public Health ; Oncology ; Original Research ; Prognosis ; Radiotherapy ; RNA, Long Noncoding - metabolism ; Stomach Neoplasms - pathology ; Tripartite Motif Proteins - genetics ; Tripartite Motif Proteins - metabolism ; Ubiquitin-Protein Ligases - genetics ; Ubiquitin-Protein Ligases - metabolism</subject><ispartof>Journal of gastrointestinal cancer, 2023-03, Vol.54 (1), p.44-50</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022</rights><rights>2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c347t-e5f5fe3a8e51d2048abff175d02a272a58202f99e0fcfd54e79aafd8e1e78cba3</citedby><cites>FETCH-LOGICAL-c347t-e5f5fe3a8e51d2048abff175d02a272a58202f99e0fcfd54e79aafd8e1e78cba3</cites><orcidid>0000-0002-6970-6998</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12029-021-00791-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12029-021-00791-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34978663$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Seifi Inallou, Mina</creatorcontrib><creatorcontrib>Safaralizadeh, Reza</creatorcontrib><creatorcontrib>Rajabi, Ali</creatorcontrib><creatorcontrib>Hosseinpourfeizi, Mohammadali</creatorcontrib><creatorcontrib>Haghi, Mehdi</creatorcontrib><title>Changes in the Expression of Long Non-Coding RNA SDMGC and Its Target Gene, TRIM16, in Patients with Gastric Cancer</title><title>Journal of gastrointestinal cancer</title><addtitle>J Gastrointest Canc</addtitle><addtitle>J Gastrointest Cancer</addtitle><description>Purpose Gastric cancer (GC) has been identified worldwide as one of the most common cancer types with a high mortality rate. LncRNA SDMGC has been recognized as an oncogene with regulatory effects on its target gene, TRIM16, which is believed to play a tumor-suppressing role in various cancers. Both these genes are involved in GC development, tumorigenesis, invasion, and metastasis. The current study is aimed to investigate the association of SDMGC and TRIM16 with GC susceptibility and GC patients’ clinicopathological characteristics. Methods A total of 100 GC tissues and their corresponding adjacent non-tumor tissues were sampled. Total RNA was then isolated to measure SDMGC and TRIM16 expression levels using quantitative reverse transcriptase (qRT)-PCR. Statistical analyses including the Mann–Whitney U test and correlation tests were carried out using R v4.5. GraphPad Prism was also used to plot the receiver operating curve (ROC). Results The results demonstrated the significant overexpression of lncRNAs SDMGC and downregulation of TRIM16 in GC tissues as compared to their corresponding marginal normal tissue samples ( P  = 0.005 and P  = 0.009, respectively). No association with clinicopathological variables was observed for either SDMGC or TRIM16. Moreover, the results demonstrated a small positive correlation between SDMGC and TRIM16. Evaluation of the diagnostic value of SDMGC and TRIM16 showed poor biomarker potency for these genes. Conclusion In conclusion, the results indicated an increase in the expression of SDMGC and a decline in the expression pattern of TRIM16 among the Iranian population. The results indicated a key tumor-accelerative function of SDMGC and a pivotal tumor-suppressing role of TRIM16 in GC patients.</description><subject>Cancer Research</subject><subject>Cell Line, Tumor</subject><subject>Gastroenterology</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Iran</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Oncology</subject><subject>Original Research</subject><subject>Prognosis</subject><subject>Radiotherapy</subject><subject>RNA, Long Noncoding - metabolism</subject><subject>Stomach Neoplasms - pathology</subject><subject>Tripartite Motif Proteins - genetics</subject><subject>Tripartite Motif Proteins - metabolism</subject><subject>Ubiquitin-Protein Ligases - genetics</subject><subject>Ubiquitin-Protein Ligases - metabolism</subject><issn>1941-6628</issn><issn>1941-6636</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1PAjEQhhujEUT_gAfTowdW2-73kay4kgAaxHNTdqewBFpsd6P8e4uLHD3NTOaZN5kHoVtKHigh8aOljLDUI4x6bkyptz9DXZoG1IsiPzo_9SzpoCtr14REQUjpJer4QRonDuoim62EWoLFlcL1CvDwe2fA2korrCUea7XEU628TJeVa2fTAX5_muQZFqrEo9riuTBLqHEOCvp4PhtNaNQ_ZL2JugLlgK-qXuFc2NpUBc6EKsBcowspNhZujrWHPp6H8-zFG7_mo2ww9go_iGsPQhlK8EUCIS0ZCRKxkJLGYUmYYDETYeLel2kKRBayDAOIUyFkmQCFOCkWwu-h-zZ3Z_RnA7bm28oWsNkIBbqxnEXUuUlcskNZixZGW2tA8p2ptsLsOSX8IJu3srmTzX9l8707ujvmN4stlKeTP7sO8FvAupWzbPhaN0a5n_-L_QHJ9Yl_</recordid><startdate>20230301</startdate><enddate>20230301</enddate><creator>Seifi Inallou, Mina</creator><creator>Safaralizadeh, Reza</creator><creator>Rajabi, Ali</creator><creator>Hosseinpourfeizi, Mohammadali</creator><creator>Haghi, Mehdi</creator><general>Springer US</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>7X8</scope><orcidid>https://orcid.org/0000-0002-6970-6998</orcidid></search><sort><creationdate>20230301</creationdate><title>Changes in the Expression of Long Non-Coding RNA SDMGC and Its Target Gene, TRIM16, in Patients with Gastric Cancer</title><author>Seifi Inallou, Mina ; Safaralizadeh, Reza ; Rajabi, Ali ; Hosseinpourfeizi, Mohammadali ; Haghi, Mehdi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c347t-e5f5fe3a8e51d2048abff175d02a272a58202f99e0fcfd54e79aafd8e1e78cba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Cancer Research</topic><topic>Cell Line, Tumor</topic><topic>Gastroenterology</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Iran</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Oncology</topic><topic>Original Research</topic><topic>Prognosis</topic><topic>Radiotherapy</topic><topic>RNA, Long Noncoding - metabolism</topic><topic>Stomach Neoplasms - pathology</topic><topic>Tripartite Motif Proteins - genetics</topic><topic>Tripartite Motif Proteins - metabolism</topic><topic>Ubiquitin-Protein Ligases - genetics</topic><topic>Ubiquitin-Protein Ligases - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seifi Inallou, Mina</creatorcontrib><creatorcontrib>Safaralizadeh, Reza</creatorcontrib><creatorcontrib>Rajabi, Ali</creatorcontrib><creatorcontrib>Hosseinpourfeizi, Mohammadali</creatorcontrib><creatorcontrib>Haghi, Mehdi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of gastrointestinal cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seifi Inallou, Mina</au><au>Safaralizadeh, Reza</au><au>Rajabi, Ali</au><au>Hosseinpourfeizi, Mohammadali</au><au>Haghi, Mehdi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in the Expression of Long Non-Coding RNA SDMGC and Its Target Gene, TRIM16, in Patients with Gastric Cancer</atitle><jtitle>Journal of gastrointestinal cancer</jtitle><stitle>J Gastrointest Canc</stitle><addtitle>J Gastrointest Cancer</addtitle><date>2023-03-01</date><risdate>2023</risdate><volume>54</volume><issue>1</issue><spage>44</spage><epage>50</epage><pages>44-50</pages><issn>1941-6628</issn><eissn>1941-6636</eissn><abstract>Purpose Gastric cancer (GC) has been identified worldwide as one of the most common cancer types with a high mortality rate. LncRNA SDMGC has been recognized as an oncogene with regulatory effects on its target gene, TRIM16, which is believed to play a tumor-suppressing role in various cancers. Both these genes are involved in GC development, tumorigenesis, invasion, and metastasis. The current study is aimed to investigate the association of SDMGC and TRIM16 with GC susceptibility and GC patients’ clinicopathological characteristics. Methods A total of 100 GC tissues and their corresponding adjacent non-tumor tissues were sampled. Total RNA was then isolated to measure SDMGC and TRIM16 expression levels using quantitative reverse transcriptase (qRT)-PCR. Statistical analyses including the Mann–Whitney U test and correlation tests were carried out using R v4.5. GraphPad Prism was also used to plot the receiver operating curve (ROC). Results The results demonstrated the significant overexpression of lncRNAs SDMGC and downregulation of TRIM16 in GC tissues as compared to their corresponding marginal normal tissue samples ( P  = 0.005 and P  = 0.009, respectively). No association with clinicopathological variables was observed for either SDMGC or TRIM16. Moreover, the results demonstrated a small positive correlation between SDMGC and TRIM16. Evaluation of the diagnostic value of SDMGC and TRIM16 showed poor biomarker potency for these genes. Conclusion In conclusion, the results indicated an increase in the expression of SDMGC and a decline in the expression pattern of TRIM16 among the Iranian population. The results indicated a key tumor-accelerative function of SDMGC and a pivotal tumor-suppressing role of TRIM16 in GC patients.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>34978663</pmid><doi>10.1007/s12029-021-00791-y</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-6970-6998</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1941-6628
ispartof Journal of gastrointestinal cancer, 2023-03, Vol.54 (1), p.44-50
issn 1941-6628
1941-6636
language eng
recordid cdi_proquest_miscellaneous_2616288048
source MEDLINE; SpringerLink Journals
subjects Cancer Research
Cell Line, Tumor
Gastroenterology
Gene Expression Regulation, Neoplastic
Humans
Internal Medicine
Iran
Medicine
Medicine & Public Health
Oncology
Original Research
Prognosis
Radiotherapy
RNA, Long Noncoding - metabolism
Stomach Neoplasms - pathology
Tripartite Motif Proteins - genetics
Tripartite Motif Proteins - metabolism
Ubiquitin-Protein Ligases - genetics
Ubiquitin-Protein Ligases - metabolism
title Changes in the Expression of Long Non-Coding RNA SDMGC and Its Target Gene, TRIM16, in Patients with Gastric Cancer
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T12%3A34%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Changes%20in%20the%20Expression%20of%20Long%20Non-Coding%20RNA%20SDMGC%20and%20Its%20Target%20Gene,%20TRIM16,%20in%20Patients%20with%20Gastric%20Cancer&rft.jtitle=Journal%20of%20gastrointestinal%20cancer&rft.au=Seifi%20Inallou,%20Mina&rft.date=2023-03-01&rft.volume=54&rft.issue=1&rft.spage=44&rft.epage=50&rft.pages=44-50&rft.issn=1941-6628&rft.eissn=1941-6636&rft_id=info:doi/10.1007/s12029-021-00791-y&rft_dat=%3Cproquest_cross%3E2616288048%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2616288048&rft_id=info:pmid/34978663&rfr_iscdi=true