EccDNA-oriented ITGB7 expression in breast cancer

Extrachromosomal circular DNA (eccDNA) is omnipresent in cancers and related to the progression of tumors and oncogene amplification. However, its function in breast cancer (BC) is unclear. After constructing the DNA library, CLeavage Effects by Circularization for Reporting of sequencing was perfor...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Annals of translational medicine 2022-12, Vol.10 (24), p.1344-1344
Hauptverfasser: Yang, Lin, Wang, Meixue, Hu, Xi'e, Yuan, Lijuan, Chen, Songhao, Peng, Shujia, Yang, Ping, Yang, Zhenyu, Bao, Guoqiang, He, Xianli
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1344
container_issue 24
container_start_page 1344
container_title Annals of translational medicine
container_volume 10
creator Yang, Lin
Wang, Meixue
Hu, Xi'e
Yuan, Lijuan
Chen, Songhao
Peng, Shujia
Yang, Ping
Yang, Zhenyu
Bao, Guoqiang
He, Xianli
description Extrachromosomal circular DNA (eccDNA) is omnipresent in cancers and related to the progression of tumors and oncogene amplification. However, its function in breast cancer (BC) is unclear. After constructing the DNA library, CLeavage Effects by Circularization for Reporting of sequencing was performed for eccDNA detection using 1 BC tissue sample. Fastqc was used to evaluate the quality of the original data. Burrows-Wheeler-Alignment Tool was used to compare the original data to the reference genome. A Circle-MAP was subsequently performed to detect eccDNA, and Bedtools was used to annotate the eccDNA genes. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses were conducted by ClusterProfiler. The Genotype-Tissue Expression and the Cancer Genome Atlas databases were used to collect the ribonucleic acid-sequencing data of the BC and normal samples. A Gene Expression Profiling Interactive Analysis, the University of Alabama at Birmingham CANcer data analysis Portal, and Kaplan-Meier survival curves were used to analyze the Cancer Genome Atlas data. A total of 200 eccDNA genes, including , were obtained. About the biological processes (BPs), these 200 genes were mainly enriched in actin cytoskeleton reorganization and axon guidance. Concerning the molecular functions (MFs), these 200 genes were mainly enriched in sodium ion transmembrane transporter activity and metal ion transmembrane transporter activity. As for cellular components (CCs), these 200 genes were mainly enriched in the transcription regulator complex and focal adhesion. was significantly enriched in cell-matrix adhesion and localization within the membrane in the BPs, integrin binding in the MFs, and cell-substrate junction and focal adhesion in the CCs. The 200 eccDNA genes were mainly enriched in the PI3K-Akt signaling pathway and focal adhesion. Notably, was enriched in focal adhesion, ECM-receptor interaction, the PI3K-Akt signaling pathway, and human papillomavirus infection. Besides, was significantly upregulated in BC patients and was associated with the menopause status of the BC patients. might serve as a prognostic marker for BC patients. has important implications for the individualized clinical treatment of BC patients.
doi_str_mv 10.21037/atm-22-5716
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9843317</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2768232342</sourcerecordid><originalsourceid>FETCH-LOGICAL-c314t-9e1d91ef779aff5e395380b0e477cccf2099f3b4a81d08c847c3c4887d7001103</originalsourceid><addsrcrecordid>eNpVkD1PwzAQhi0Eoqh0Y0YZGTDYviS2F6RSSqlUwVJmy3EuEJSPYqcI_j2BlqpMPsmP3nvvIeSMsyvBGchr29VUCJpInh6QEwEsoYkCfbg3D8gohDfGGBdcA2PHZABpmrJUJSeET527exzT1pfYdJhH8-XsVkb4ufIYQtk2UdlEmUcbusjZxqE_JUeFrQKOtu-QPN9Pl5MHuniazSfjBXXA445q5LnmWEipbVEkCDoBxTKGsZTOuUIwrQvIYqt4zpRTsXTgYqVkLvum_W1DcrPJXa2zGnPX1_O2Mitf1tZ_mdaW5v9PU76al_bDaBUDcNkHXGwDfPu-xtCZugwOq8o22K6DETJVAgTEokcvN6jzbQgei90azsyvaNOLNkKYH9E9fr5fbQf_aYVvJJN33A</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2768232342</pqid></control><display><type>article</type><title>EccDNA-oriented ITGB7 expression in breast cancer</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Yang, Lin ; Wang, Meixue ; Hu, Xi'e ; Yuan, Lijuan ; Chen, Songhao ; Peng, Shujia ; Yang, Ping ; Yang, Zhenyu ; Bao, Guoqiang ; He, Xianli</creator><creatorcontrib>Yang, Lin ; Wang, Meixue ; Hu, Xi'e ; Yuan, Lijuan ; Chen, Songhao ; Peng, Shujia ; Yang, Ping ; Yang, Zhenyu ; Bao, Guoqiang ; He, Xianli</creatorcontrib><description>Extrachromosomal circular DNA (eccDNA) is omnipresent in cancers and related to the progression of tumors and oncogene amplification. However, its function in breast cancer (BC) is unclear. After constructing the DNA library, CLeavage Effects by Circularization for Reporting of sequencing was performed for eccDNA detection using 1 BC tissue sample. Fastqc was used to evaluate the quality of the original data. Burrows-Wheeler-Alignment Tool was used to compare the original data to the reference genome. A Circle-MAP was subsequently performed to detect eccDNA, and Bedtools was used to annotate the eccDNA genes. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses were conducted by ClusterProfiler. The Genotype-Tissue Expression and the Cancer Genome Atlas databases were used to collect the ribonucleic acid-sequencing data of the BC and normal samples. A Gene Expression Profiling Interactive Analysis, the University of Alabama at Birmingham CANcer data analysis Portal, and Kaplan-Meier survival curves were used to analyze the Cancer Genome Atlas data. A total of 200 eccDNA genes, including , were obtained. About the biological processes (BPs), these 200 genes were mainly enriched in actin cytoskeleton reorganization and axon guidance. Concerning the molecular functions (MFs), these 200 genes were mainly enriched in sodium ion transmembrane transporter activity and metal ion transmembrane transporter activity. As for cellular components (CCs), these 200 genes were mainly enriched in the transcription regulator complex and focal adhesion. was significantly enriched in cell-matrix adhesion and localization within the membrane in the BPs, integrin binding in the MFs, and cell-substrate junction and focal adhesion in the CCs. The 200 eccDNA genes were mainly enriched in the PI3K-Akt signaling pathway and focal adhesion. Notably, was enriched in focal adhesion, ECM-receptor interaction, the PI3K-Akt signaling pathway, and human papillomavirus infection. Besides, was significantly upregulated in BC patients and was associated with the menopause status of the BC patients. might serve as a prognostic marker for BC patients. has important implications for the individualized clinical treatment of BC patients.</description><identifier>ISSN: 2305-5839</identifier><identifier>EISSN: 2305-5839</identifier><identifier>DOI: 10.21037/atm-22-5716</identifier><identifier>PMID: 36660685</identifier><language>eng</language><publisher>China: AME Publishing Company</publisher><subject>Original</subject><ispartof>Annals of translational medicine, 2022-12, Vol.10 (24), p.1344-1344</ispartof><rights>2022 Annals of Translational Medicine. All rights reserved.</rights><rights>2022 Annals of Translational Medicine. All rights reserved. 2022 Annals of Translational Medicine.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c314t-9e1d91ef779aff5e395380b0e477cccf2099f3b4a81d08c847c3c4887d7001103</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/PMC9843317/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9843317/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36660685$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Lin</creatorcontrib><creatorcontrib>Wang, Meixue</creatorcontrib><creatorcontrib>Hu, Xi'e</creatorcontrib><creatorcontrib>Yuan, Lijuan</creatorcontrib><creatorcontrib>Chen, Songhao</creatorcontrib><creatorcontrib>Peng, Shujia</creatorcontrib><creatorcontrib>Yang, Ping</creatorcontrib><creatorcontrib>Yang, Zhenyu</creatorcontrib><creatorcontrib>Bao, Guoqiang</creatorcontrib><creatorcontrib>He, Xianli</creatorcontrib><title>EccDNA-oriented ITGB7 expression in breast cancer</title><title>Annals of translational medicine</title><addtitle>Ann Transl Med</addtitle><description>Extrachromosomal circular DNA (eccDNA) is omnipresent in cancers and related to the progression of tumors and oncogene amplification. However, its function in breast cancer (BC) is unclear. After constructing the DNA library, CLeavage Effects by Circularization for Reporting of sequencing was performed for eccDNA detection using 1 BC tissue sample. Fastqc was used to evaluate the quality of the original data. Burrows-Wheeler-Alignment Tool was used to compare the original data to the reference genome. A Circle-MAP was subsequently performed to detect eccDNA, and Bedtools was used to annotate the eccDNA genes. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses were conducted by ClusterProfiler. The Genotype-Tissue Expression and the Cancer Genome Atlas databases were used to collect the ribonucleic acid-sequencing data of the BC and normal samples. A Gene Expression Profiling Interactive Analysis, the University of Alabama at Birmingham CANcer data analysis Portal, and Kaplan-Meier survival curves were used to analyze the Cancer Genome Atlas data. A total of 200 eccDNA genes, including , were obtained. About the biological processes (BPs), these 200 genes were mainly enriched in actin cytoskeleton reorganization and axon guidance. Concerning the molecular functions (MFs), these 200 genes were mainly enriched in sodium ion transmembrane transporter activity and metal ion transmembrane transporter activity. As for cellular components (CCs), these 200 genes were mainly enriched in the transcription regulator complex and focal adhesion. was significantly enriched in cell-matrix adhesion and localization within the membrane in the BPs, integrin binding in the MFs, and cell-substrate junction and focal adhesion in the CCs. The 200 eccDNA genes were mainly enriched in the PI3K-Akt signaling pathway and focal adhesion. Notably, was enriched in focal adhesion, ECM-receptor interaction, the PI3K-Akt signaling pathway, and human papillomavirus infection. Besides, was significantly upregulated in BC patients and was associated with the menopause status of the BC patients. might serve as a prognostic marker for BC patients. has important implications for the individualized clinical treatment of BC patients.</description><subject>Original</subject><issn>2305-5839</issn><issn>2305-5839</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpVkD1PwzAQhi0Eoqh0Y0YZGTDYviS2F6RSSqlUwVJmy3EuEJSPYqcI_j2BlqpMPsmP3nvvIeSMsyvBGchr29VUCJpInh6QEwEsoYkCfbg3D8gohDfGGBdcA2PHZABpmrJUJSeET527exzT1pfYdJhH8-XsVkb4ufIYQtk2UdlEmUcbusjZxqE_JUeFrQKOtu-QPN9Pl5MHuniazSfjBXXA445q5LnmWEipbVEkCDoBxTKGsZTOuUIwrQvIYqt4zpRTsXTgYqVkLvum_W1DcrPJXa2zGnPX1_O2Mitf1tZ_mdaW5v9PU76al_bDaBUDcNkHXGwDfPu-xtCZugwOq8o22K6DETJVAgTEokcvN6jzbQgei90azsyvaNOLNkKYH9E9fr5fbQf_aYVvJJN33A</recordid><startdate>20221201</startdate><enddate>20221201</enddate><creator>Yang, Lin</creator><creator>Wang, Meixue</creator><creator>Hu, Xi'e</creator><creator>Yuan, Lijuan</creator><creator>Chen, Songhao</creator><creator>Peng, Shujia</creator><creator>Yang, Ping</creator><creator>Yang, Zhenyu</creator><creator>Bao, Guoqiang</creator><creator>He, Xianli</creator><general>AME Publishing Company</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20221201</creationdate><title>EccDNA-oriented ITGB7 expression in breast cancer</title><author>Yang, Lin ; Wang, Meixue ; Hu, Xi'e ; Yuan, Lijuan ; Chen, Songhao ; Peng, Shujia ; Yang, Ping ; Yang, Zhenyu ; Bao, Guoqiang ; He, Xianli</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c314t-9e1d91ef779aff5e395380b0e477cccf2099f3b4a81d08c847c3c4887d7001103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Original</topic><toplevel>online_resources</toplevel><creatorcontrib>Yang, Lin</creatorcontrib><creatorcontrib>Wang, Meixue</creatorcontrib><creatorcontrib>Hu, Xi'e</creatorcontrib><creatorcontrib>Yuan, Lijuan</creatorcontrib><creatorcontrib>Chen, Songhao</creatorcontrib><creatorcontrib>Peng, Shujia</creatorcontrib><creatorcontrib>Yang, Ping</creatorcontrib><creatorcontrib>Yang, Zhenyu</creatorcontrib><creatorcontrib>Bao, Guoqiang</creatorcontrib><creatorcontrib>He, Xianli</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Annals of translational medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Lin</au><au>Wang, Meixue</au><au>Hu, Xi'e</au><au>Yuan, Lijuan</au><au>Chen, Songhao</au><au>Peng, Shujia</au><au>Yang, Ping</au><au>Yang, Zhenyu</au><au>Bao, Guoqiang</au><au>He, Xianli</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>EccDNA-oriented ITGB7 expression in breast cancer</atitle><jtitle>Annals of translational medicine</jtitle><addtitle>Ann Transl Med</addtitle><date>2022-12-01</date><risdate>2022</risdate><volume>10</volume><issue>24</issue><spage>1344</spage><epage>1344</epage><pages>1344-1344</pages><issn>2305-5839</issn><eissn>2305-5839</eissn><abstract>Extrachromosomal circular DNA (eccDNA) is omnipresent in cancers and related to the progression of tumors and oncogene amplification. However, its function in breast cancer (BC) is unclear. After constructing the DNA library, CLeavage Effects by Circularization for Reporting of sequencing was performed for eccDNA detection using 1 BC tissue sample. Fastqc was used to evaluate the quality of the original data. Burrows-Wheeler-Alignment Tool was used to compare the original data to the reference genome. A Circle-MAP was subsequently performed to detect eccDNA, and Bedtools was used to annotate the eccDNA genes. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses were conducted by ClusterProfiler. The Genotype-Tissue Expression and the Cancer Genome Atlas databases were used to collect the ribonucleic acid-sequencing data of the BC and normal samples. A Gene Expression Profiling Interactive Analysis, the University of Alabama at Birmingham CANcer data analysis Portal, and Kaplan-Meier survival curves were used to analyze the Cancer Genome Atlas data. A total of 200 eccDNA genes, including , were obtained. About the biological processes (BPs), these 200 genes were mainly enriched in actin cytoskeleton reorganization and axon guidance. Concerning the molecular functions (MFs), these 200 genes were mainly enriched in sodium ion transmembrane transporter activity and metal ion transmembrane transporter activity. As for cellular components (CCs), these 200 genes were mainly enriched in the transcription regulator complex and focal adhesion. was significantly enriched in cell-matrix adhesion and localization within the membrane in the BPs, integrin binding in the MFs, and cell-substrate junction and focal adhesion in the CCs. The 200 eccDNA genes were mainly enriched in the PI3K-Akt signaling pathway and focal adhesion. Notably, was enriched in focal adhesion, ECM-receptor interaction, the PI3K-Akt signaling pathway, and human papillomavirus infection. Besides, was significantly upregulated in BC patients and was associated with the menopause status of the BC patients. might serve as a prognostic marker for BC patients. has important implications for the individualized clinical treatment of BC patients.</abstract><cop>China</cop><pub>AME Publishing Company</pub><pmid>36660685</pmid><doi>10.21037/atm-22-5716</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2305-5839
ispartof Annals of translational medicine, 2022-12, Vol.10 (24), p.1344-1344
issn 2305-5839
2305-5839
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9843317
source Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Original
title EccDNA-oriented ITGB7 expression in breast cancer
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T22%3A58%3A58IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=EccDNA-oriented%20ITGB7%20expression%20in%20breast%20cancer&rft.jtitle=Annals%20of%20translational%20medicine&rft.au=Yang,%20Lin&rft.date=2022-12-01&rft.volume=10&rft.issue=24&rft.spage=1344&rft.epage=1344&rft.pages=1344-1344&rft.issn=2305-5839&rft.eissn=2305-5839&rft_id=info:doi/10.21037/atm-22-5716&rft_dat=%3Cproquest_pubme%3E2768232342%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2768232342&rft_id=info:pmid/36660685&rfr_iscdi=true