Loading…

Bioinformatics analysis of the prognosis and biological significance of HMGB1, HMGB2, and HMGB3 in gastric cancer

High mobility group box (HMGB) consists primarily of HMGB1, HMGB2, and HMGB3 proteins. Although abnormal HMGB expression is associated with various tumors, the relationship with gastric cancer (GC) remains unclear. In this study, HMGB1, HMGB2, and HMGB3 expression was analyzed using the Oncomine and...

Full description

Saved in:
Bibliographic Details
Published in:Journal of cellular physiology 2020-04, Vol.235 (4), p.3438-3446
Main Authors: Fang, Jian, Ge, Xuhui, Xu, Wenjing, Xie, Jingjing, Qin, Zhongke, Shi, Liqing, Yin, Wenjie, Bian, Maohong, Wang, Hao
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c3533-c026090f180d2ba8807bab96fe76dbf95d5e82c84d40ca35747740bdc5dbbfd3
cites cdi_FETCH-LOGICAL-c3533-c026090f180d2ba8807bab96fe76dbf95d5e82c84d40ca35747740bdc5dbbfd3
container_end_page 3446
container_issue 4
container_start_page 3438
container_title Journal of cellular physiology
container_volume 235
creator Fang, Jian
Ge, Xuhui
Xu, Wenjing
Xie, Jingjing
Qin, Zhongke
Shi, Liqing
Yin, Wenjie
Bian, Maohong
Wang, Hao
description High mobility group box (HMGB) consists primarily of HMGB1, HMGB2, and HMGB3 proteins. Although abnormal HMGB expression is associated with various tumors, the relationship with gastric cancer (GC) remains unclear. In this study, HMGB1, HMGB2, and HMGB3 expression was analyzed using the Oncomine and TCGA databases. Correlations between HMGB1, HMGB2, and HMGB3 and clinicopathological factors were analyzed. cBioPortal was used to analyze HMGB1, HMGB2, and HMGB3 genetic alterations and its gene regulation network in GC tissue. HMGB1, HMGB2, and HMGB3 expression was higher in tumor tissues than in normal tissues, especially in GC. High HMGB1, HMGB2, and HMGB3 expression may predict a poor prognosis among patients with GC (hazard ratios [HR] = 1.90; 95% confidence interval [CI]: [1.30−2.78]) and human digestive system neoplasm (HR = 1.85; 95% CI [1.64−2.10]). These findings suggest that HMGB1, HMGB2, and HMGB3 may be useful prognostic indicators for patients with GC. HMGB1, HMGB2, and HMGB3 expression was higher in tumor tissues than in normal tissues, especially in gastric cancer (GC). High HMGB1, HMGB2, and HMGB3 expression may predict a poor prognosis among patients with GC and human digestive system neoplasm. These findings suggest that HMGB1, HMGB2, and HMGB3 may be useful prognostic indicators for patients with GC.
doi_str_mv 10.1002/jcp.29233
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2306492084</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2333563692</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3533-c026090f180d2ba8807bab96fe76dbf95d5e82c84d40ca35747740bdc5dbbfd3</originalsourceid><addsrcrecordid>eNp10U1PGzEQBmCrKmpCyqF_oLLUS5FYGNu73vURIkhAoHLIfeXP1NFmHexEVf493gR6QOI0I8-jV_IMQj8IXBIAerXSm0sqKGNf0JiAqIuSV_QrGucZKURVkhE6TWkFAEIw9g2NGOGUQM3H6OXGB9-7ENdy63XCspfdPvmEg8PbvxZvYlj2YXiQvcHKhy4svZYdTn7Ze5fbXtsBz59mN-TiUOjFAQ8tw77HS5m20Wt8sPE7OnGyS_bsrU7Q4u52MZ0Xj39m99Prx0KzirFCA-UgwJEGDFWyaaBWUgnubM2NcqIylW2obkpTgpasqsu6LkEZXRmlnGET9PsYm3_wsrNp26590rbrZG_DLrWUAS8FhabM9NcHugq7mBcxKMYqznhe7gSdH5WOIaVoXbuJfi3jviXQDmdo8xnawxmy_fmWuFNra_7L971ncHUE_3xn958ntQ_T52PkK2xlj5A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2333563692</pqid></control><display><type>article</type><title>Bioinformatics analysis of the prognosis and biological significance of HMGB1, HMGB2, and HMGB3 in gastric cancer</title><source>Wiley</source><creator>Fang, Jian ; Ge, Xuhui ; Xu, Wenjing ; Xie, Jingjing ; Qin, Zhongke ; Shi, Liqing ; Yin, Wenjie ; Bian, Maohong ; Wang, Hao</creator><creatorcontrib>Fang, Jian ; Ge, Xuhui ; Xu, Wenjing ; Xie, Jingjing ; Qin, Zhongke ; Shi, Liqing ; Yin, Wenjie ; Bian, Maohong ; Wang, Hao</creatorcontrib><description>High mobility group box (HMGB) consists primarily of HMGB1, HMGB2, and HMGB3 proteins. Although abnormal HMGB expression is associated with various tumors, the relationship with gastric cancer (GC) remains unclear. In this study, HMGB1, HMGB2, and HMGB3 expression was analyzed using the Oncomine and TCGA databases. Correlations between HMGB1, HMGB2, and HMGB3 and clinicopathological factors were analyzed. cBioPortal was used to analyze HMGB1, HMGB2, and HMGB3 genetic alterations and its gene regulation network in GC tissue. HMGB1, HMGB2, and HMGB3 expression was higher in tumor tissues than in normal tissues, especially in GC. High HMGB1, HMGB2, and HMGB3 expression may predict a poor prognosis among patients with GC (hazard ratios [HR] = 1.90; 95% confidence interval [CI]: [1.30−2.78]) and human digestive system neoplasm (HR = 1.85; 95% CI [1.64−2.10]). These findings suggest that HMGB1, HMGB2, and HMGB3 may be useful prognostic indicators for patients with GC. HMGB1, HMGB2, and HMGB3 expression was higher in tumor tissues than in normal tissues, especially in gastric cancer (GC). High HMGB1, HMGB2, and HMGB3 expression may predict a poor prognosis among patients with GC and human digestive system neoplasm. These findings suggest that HMGB1, HMGB2, and HMGB3 may be useful prognostic indicators for patients with GC.</description><identifier>ISSN: 0021-9541</identifier><identifier>EISSN: 1097-4652</identifier><identifier>DOI: 10.1002/jcp.29233</identifier><identifier>PMID: 31621076</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Bioinformatics ; Cancer ; Cell Line, Tumor ; Cell Proliferation ; Computational Biology ; Confidence intervals ; Digestive system ; Female ; Gastric cancer ; Gene expression ; Gene Expression Regulation, Neoplastic - genetics ; Gene regulation ; high mobility group boxes ; High mobility group proteins ; HMGB1 protein ; HMGB1 Protein - genetics ; HMGB2 Protein - genetics ; HMGB3 Protein - genetics ; Humans ; Male ; Medical prognosis ; Neoplasia ; Prognosis ; Progression-Free Survival ; Proportional Hazards Models ; Stomach Neoplasms - genetics ; Stomach Neoplasms - pathology ; Tumors</subject><ispartof>Journal of cellular physiology, 2020-04, Vol.235 (4), p.3438-3446</ispartof><rights>2019 Wiley Periodicals, Inc.</rights><rights>2020 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3533-c026090f180d2ba8807bab96fe76dbf95d5e82c84d40ca35747740bdc5dbbfd3</citedby><cites>FETCH-LOGICAL-c3533-c026090f180d2ba8807bab96fe76dbf95d5e82c84d40ca35747740bdc5dbbfd3</cites><orcidid>0000-0001-7598-1091</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31621076$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fang, Jian</creatorcontrib><creatorcontrib>Ge, Xuhui</creatorcontrib><creatorcontrib>Xu, Wenjing</creatorcontrib><creatorcontrib>Xie, Jingjing</creatorcontrib><creatorcontrib>Qin, Zhongke</creatorcontrib><creatorcontrib>Shi, Liqing</creatorcontrib><creatorcontrib>Yin, Wenjie</creatorcontrib><creatorcontrib>Bian, Maohong</creatorcontrib><creatorcontrib>Wang, Hao</creatorcontrib><title>Bioinformatics analysis of the prognosis and biological significance of HMGB1, HMGB2, and HMGB3 in gastric cancer</title><title>Journal of cellular physiology</title><addtitle>J Cell Physiol</addtitle><description>High mobility group box (HMGB) consists primarily of HMGB1, HMGB2, and HMGB3 proteins. Although abnormal HMGB expression is associated with various tumors, the relationship with gastric cancer (GC) remains unclear. In this study, HMGB1, HMGB2, and HMGB3 expression was analyzed using the Oncomine and TCGA databases. Correlations between HMGB1, HMGB2, and HMGB3 and clinicopathological factors were analyzed. cBioPortal was used to analyze HMGB1, HMGB2, and HMGB3 genetic alterations and its gene regulation network in GC tissue. HMGB1, HMGB2, and HMGB3 expression was higher in tumor tissues than in normal tissues, especially in GC. High HMGB1, HMGB2, and HMGB3 expression may predict a poor prognosis among patients with GC (hazard ratios [HR] = 1.90; 95% confidence interval [CI]: [1.30−2.78]) and human digestive system neoplasm (HR = 1.85; 95% CI [1.64−2.10]). These findings suggest that HMGB1, HMGB2, and HMGB3 may be useful prognostic indicators for patients with GC. HMGB1, HMGB2, and HMGB3 expression was higher in tumor tissues than in normal tissues, especially in gastric cancer (GC). High HMGB1, HMGB2, and HMGB3 expression may predict a poor prognosis among patients with GC and human digestive system neoplasm. These findings suggest that HMGB1, HMGB2, and HMGB3 may be useful prognostic indicators for patients with GC.</description><subject>Bioinformatics</subject><subject>Cancer</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation</subject><subject>Computational Biology</subject><subject>Confidence intervals</subject><subject>Digestive system</subject><subject>Female</subject><subject>Gastric cancer</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Neoplastic - genetics</subject><subject>Gene regulation</subject><subject>high mobility group boxes</subject><subject>High mobility group proteins</subject><subject>HMGB1 protein</subject><subject>HMGB1 Protein - genetics</subject><subject>HMGB2 Protein - genetics</subject><subject>HMGB3 Protein - genetics</subject><subject>Humans</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Neoplasia</subject><subject>Prognosis</subject><subject>Progression-Free Survival</subject><subject>Proportional Hazards Models</subject><subject>Stomach Neoplasms - genetics</subject><subject>Stomach Neoplasms - pathology</subject><subject>Tumors</subject><issn>0021-9541</issn><issn>1097-4652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp10U1PGzEQBmCrKmpCyqF_oLLUS5FYGNu73vURIkhAoHLIfeXP1NFmHexEVf493gR6QOI0I8-jV_IMQj8IXBIAerXSm0sqKGNf0JiAqIuSV_QrGucZKURVkhE6TWkFAEIw9g2NGOGUQM3H6OXGB9-7ENdy63XCspfdPvmEg8PbvxZvYlj2YXiQvcHKhy4svZYdTn7Ze5fbXtsBz59mN-TiUOjFAQ8tw77HS5m20Wt8sPE7OnGyS_bsrU7Q4u52MZ0Xj39m99Prx0KzirFCA-UgwJEGDFWyaaBWUgnubM2NcqIylW2obkpTgpasqsu6LkEZXRmlnGET9PsYm3_wsrNp26590rbrZG_DLrWUAS8FhabM9NcHugq7mBcxKMYqznhe7gSdH5WOIaVoXbuJfi3jviXQDmdo8xnawxmy_fmWuFNra_7L971ncHUE_3xn958ntQ_T52PkK2xlj5A</recordid><startdate>202004</startdate><enddate>202004</enddate><creator>Fang, Jian</creator><creator>Ge, Xuhui</creator><creator>Xu, Wenjing</creator><creator>Xie, Jingjing</creator><creator>Qin, Zhongke</creator><creator>Shi, Liqing</creator><creator>Yin, Wenjie</creator><creator>Bian, Maohong</creator><creator>Wang, Hao</creator><general>Wiley Subscription Services, Inc</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>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7598-1091</orcidid></search><sort><creationdate>202004</creationdate><title>Bioinformatics analysis of the prognosis and biological significance of HMGB1, HMGB2, and HMGB3 in gastric cancer</title><author>Fang, Jian ; Ge, Xuhui ; Xu, Wenjing ; Xie, Jingjing ; Qin, Zhongke ; Shi, Liqing ; Yin, Wenjie ; Bian, Maohong ; Wang, Hao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3533-c026090f180d2ba8807bab96fe76dbf95d5e82c84d40ca35747740bdc5dbbfd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Bioinformatics</topic><topic>Cancer</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation</topic><topic>Computational Biology</topic><topic>Confidence intervals</topic><topic>Digestive system</topic><topic>Female</topic><topic>Gastric cancer</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Neoplastic - genetics</topic><topic>Gene regulation</topic><topic>high mobility group boxes</topic><topic>High mobility group proteins</topic><topic>HMGB1 protein</topic><topic>HMGB1 Protein - genetics</topic><topic>HMGB2 Protein - genetics</topic><topic>HMGB3 Protein - genetics</topic><topic>Humans</topic><topic>Male</topic><topic>Medical prognosis</topic><topic>Neoplasia</topic><topic>Prognosis</topic><topic>Progression-Free Survival</topic><topic>Proportional Hazards Models</topic><topic>Stomach Neoplasms - genetics</topic><topic>Stomach Neoplasms - pathology</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fang, Jian</creatorcontrib><creatorcontrib>Ge, Xuhui</creatorcontrib><creatorcontrib>Xu, Wenjing</creatorcontrib><creatorcontrib>Xie, Jingjing</creatorcontrib><creatorcontrib>Qin, Zhongke</creatorcontrib><creatorcontrib>Shi, Liqing</creatorcontrib><creatorcontrib>Yin, Wenjie</creatorcontrib><creatorcontrib>Bian, Maohong</creatorcontrib><creatorcontrib>Wang, Hao</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cellular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fang, Jian</au><au>Ge, Xuhui</au><au>Xu, Wenjing</au><au>Xie, Jingjing</au><au>Qin, Zhongke</au><au>Shi, Liqing</au><au>Yin, Wenjie</au><au>Bian, Maohong</au><au>Wang, Hao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bioinformatics analysis of the prognosis and biological significance of HMGB1, HMGB2, and HMGB3 in gastric cancer</atitle><jtitle>Journal of cellular physiology</jtitle><addtitle>J Cell Physiol</addtitle><date>2020-04</date><risdate>2020</risdate><volume>235</volume><issue>4</issue><spage>3438</spage><epage>3446</epage><pages>3438-3446</pages><issn>0021-9541</issn><eissn>1097-4652</eissn><abstract>High mobility group box (HMGB) consists primarily of HMGB1, HMGB2, and HMGB3 proteins. Although abnormal HMGB expression is associated with various tumors, the relationship with gastric cancer (GC) remains unclear. In this study, HMGB1, HMGB2, and HMGB3 expression was analyzed using the Oncomine and TCGA databases. Correlations between HMGB1, HMGB2, and HMGB3 and clinicopathological factors were analyzed. cBioPortal was used to analyze HMGB1, HMGB2, and HMGB3 genetic alterations and its gene regulation network in GC tissue. HMGB1, HMGB2, and HMGB3 expression was higher in tumor tissues than in normal tissues, especially in GC. High HMGB1, HMGB2, and HMGB3 expression may predict a poor prognosis among patients with GC (hazard ratios [HR] = 1.90; 95% confidence interval [CI]: [1.30−2.78]) and human digestive system neoplasm (HR = 1.85; 95% CI [1.64−2.10]). These findings suggest that HMGB1, HMGB2, and HMGB3 may be useful prognostic indicators for patients with GC. HMGB1, HMGB2, and HMGB3 expression was higher in tumor tissues than in normal tissues, especially in gastric cancer (GC). High HMGB1, HMGB2, and HMGB3 expression may predict a poor prognosis among patients with GC and human digestive system neoplasm. These findings suggest that HMGB1, HMGB2, and HMGB3 may be useful prognostic indicators for patients with GC.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31621076</pmid><doi>10.1002/jcp.29233</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-7598-1091</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0021-9541
ispartof Journal of cellular physiology, 2020-04, Vol.235 (4), p.3438-3446
issn 0021-9541
1097-4652
language eng
recordid cdi_proquest_miscellaneous_2306492084
source Wiley
subjects Bioinformatics
Cancer
Cell Line, Tumor
Cell Proliferation
Computational Biology
Confidence intervals
Digestive system
Female
Gastric cancer
Gene expression
Gene Expression Regulation, Neoplastic - genetics
Gene regulation
high mobility group boxes
High mobility group proteins
HMGB1 protein
HMGB1 Protein - genetics
HMGB2 Protein - genetics
HMGB3 Protein - genetics
Humans
Male
Medical prognosis
Neoplasia
Prognosis
Progression-Free Survival
Proportional Hazards Models
Stomach Neoplasms - genetics
Stomach Neoplasms - pathology
Tumors
title Bioinformatics analysis of the prognosis and biological significance of HMGB1, HMGB2, and HMGB3 in gastric cancer
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T17%3A10%3A45IST&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=Bioinformatics%20analysis%20of%20the%20prognosis%20and%20biological%20significance%20of%20HMGB1,%20HMGB2,%20and%20HMGB3%20in%20gastric%20cancer&rft.jtitle=Journal%20of%20cellular%20physiology&rft.au=Fang,%20Jian&rft.date=2020-04&rft.volume=235&rft.issue=4&rft.spage=3438&rft.epage=3446&rft.pages=3438-3446&rft.issn=0021-9541&rft.eissn=1097-4652&rft_id=info:doi/10.1002/jcp.29233&rft_dat=%3Cproquest_cross%3E2333563692%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3533-c026090f180d2ba8807bab96fe76dbf95d5e82c84d40ca35747740bdc5dbbfd3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2333563692&rft_id=info:pmid/31621076&rfr_iscdi=true