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An Integrative Pan-Cancer Analysis of the Oncogenic Role of COPB2 in Human Tumors
Several studies have suggested that coatomer protein complex subunit beta 2 (COPB2) may act as an oncogene in various cancer types. However, no systematic pan-cancer analysis has been performed to date. Therefore, the present study analyzed the potential oncogenic role of COPB2 using TCGA (The Cance...
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Published in: | BioMed research international 2021, Vol.2021 (1), p.7405322-7405322 |
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description | Several studies have suggested that coatomer protein complex subunit beta 2 (COPB2) may act as an oncogene in various cancer types. However, no systematic pan-cancer analysis has been performed to date. Therefore, the present study analyzed the potential oncogenic role of COPB2 using TCGA (The Cancer Genome Atlas) and GEO (Gene Expression Omnibus) datasets. The majority of the cancer types overexpressed the COPB2 protein, and its expression significantly correlated with tumor prognosis. In certain tumors, such as those found in breast and ovarian tissues, phosphorylated S859 exhibited high expression. It was found that mutations of the COPB2 protein in kidney and endometrial cancers exhibited a significant impact on patient prognosis. It is interesting to note that COPB2 expression correlated with the number of cancer-associated fibroblasts in certain tumors, such as cervical and endocervical cancers and colon adenocarcinomas. In addition, COPB2 was involved in the transport of substances and correlated with chemotherapy sensitivity. This is considered the first pan-tumor study, which provided a relatively comprehensive understanding of the mechanism by which COPB2 promotes cancer growth. |
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However, no systematic pan-cancer analysis has been performed to date. Therefore, the present study analyzed the potential oncogenic role of COPB2 using TCGA (The Cancer Genome Atlas) and GEO (Gene Expression Omnibus) datasets. The majority of the cancer types overexpressed the COPB2 protein, and its expression significantly correlated with tumor prognosis. In certain tumors, such as those found in breast and ovarian tissues, phosphorylated S859 exhibited high expression. It was found that mutations of the COPB2 protein in kidney and endometrial cancers exhibited a significant impact on patient prognosis. It is interesting to note that COPB2 expression correlated with the number of cancer-associated fibroblasts in certain tumors, such as cervical and endocervical cancers and colon adenocarcinomas. In addition, COPB2 was involved in the transport of substances and correlated with chemotherapy sensitivity. This is considered the first pan-tumor study, which provided a relatively comprehensive understanding of the mechanism by which COPB2 promotes cancer growth.</description><identifier>ISSN: 2314-6133</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2021/7405322</identifier><identifier>PMID: 34676262</identifier><language>eng</language><publisher>United States: Hindawi</publisher><subject>Analysis ; Binding proteins ; Biomedical research ; Breast ; Cancer ; Carcinogenesis ; Cervix ; Chemotherapy ; Coatomer Protein - genetics ; Coatomer Protein - metabolism ; Colon ; Computational Biology ; Databases, Genetic ; Datasets ; Diagnosis ; Endometrial cancer ; Endometrium ; Fibroblasts ; Gene expression ; Genetic aspects ; Genomes ; Health aspects ; Humans ; Identification and classification ; Molecular Targeted Therapy - methods ; Mutation ; Neoplasms - genetics ; Neoplasms - metabolism ; Neoplasms - pathology ; Oncogenes ; Ovarian cancer ; Physiological aspects ; Prognosis ; Proteins ; Survival Rate ; Transforming growth factors ; Tumors</subject><ispartof>BioMed research international, 2021, Vol.2021 (1), p.7405322-7405322</ispartof><rights>Copyright © 2021 Biao Wu et al.</rights><rights>COPYRIGHT 2021 John Wiley & Sons, Inc.</rights><rights>Copyright © 2021 Biao Wu et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2021 Biao Wu et al. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c504t-3656ca073099cd1612885263ad170be1eb79ce0a0a7c5817015a7ae278c276693</citedby><cites>FETCH-LOGICAL-c504t-3656ca073099cd1612885263ad170be1eb79ce0a0a7c5817015a7ae278c276693</cites><orcidid>0000-0001-8475-4747 ; 0000-0003-0182-9454 ; 0000-0001-7648-365X ; 0000-0003-1821-9759</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2585198602/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2585198602?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,4021,25751,27921,27922,27923,37010,37011,44588,74896</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34676262$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Ma, Yong Xin</contributor><contributor>Yong Xin Ma</contributor><creatorcontrib>Wu, Biao</creatorcontrib><creatorcontrib>Wu, Yumeng</creatorcontrib><creatorcontrib>Guo, Xianlin</creatorcontrib><creatorcontrib>Yue, Yanping</creatorcontrib><creatorcontrib>Li, Yuanyuan</creatorcontrib><creatorcontrib>He, Xiao</creatorcontrib><creatorcontrib>Chen, Yuanbin</creatorcontrib><creatorcontrib>Zhao, Wenjing</creatorcontrib><creatorcontrib>Liu, Jibin</creatorcontrib><creatorcontrib>Wu, Xuming</creatorcontrib><creatorcontrib>Shen, Aiguo</creatorcontrib><creatorcontrib>Zhang, Suqing</creatorcontrib><title>An Integrative Pan-Cancer Analysis of the Oncogenic Role of COPB2 in Human Tumors</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><description>Several studies have suggested that coatomer protein complex subunit beta 2 (COPB2) may act as an oncogene in various cancer types. However, no systematic pan-cancer analysis has been performed to date. Therefore, the present study analyzed the potential oncogenic role of COPB2 using TCGA (The Cancer Genome Atlas) and GEO (Gene Expression Omnibus) datasets. The majority of the cancer types overexpressed the COPB2 protein, and its expression significantly correlated with tumor prognosis. In certain tumors, such as those found in breast and ovarian tissues, phosphorylated S859 exhibited high expression. It was found that mutations of the COPB2 protein in kidney and endometrial cancers exhibited a significant impact on patient prognosis. It is interesting to note that COPB2 expression correlated with the number of cancer-associated fibroblasts in certain tumors, such as cervical and endocervical cancers and colon adenocarcinomas. In addition, COPB2 was involved in the transport of substances and correlated with chemotherapy sensitivity. 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However, no systematic pan-cancer analysis has been performed to date. Therefore, the present study analyzed the potential oncogenic role of COPB2 using TCGA (The Cancer Genome Atlas) and GEO (Gene Expression Omnibus) datasets. The majority of the cancer types overexpressed the COPB2 protein, and its expression significantly correlated with tumor prognosis. In certain tumors, such as those found in breast and ovarian tissues, phosphorylated S859 exhibited high expression. It was found that mutations of the COPB2 protein in kidney and endometrial cancers exhibited a significant impact on patient prognosis. It is interesting to note that COPB2 expression correlated with the number of cancer-associated fibroblasts in certain tumors, such as cervical and endocervical cancers and colon adenocarcinomas. In addition, COPB2 was involved in the transport of substances and correlated with chemotherapy sensitivity. 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subjects | Analysis Binding proteins Biomedical research Breast Cancer Carcinogenesis Cervix Chemotherapy Coatomer Protein - genetics Coatomer Protein - metabolism Colon Computational Biology Databases, Genetic Datasets Diagnosis Endometrial cancer Endometrium Fibroblasts Gene expression Genetic aspects Genomes Health aspects Humans Identification and classification Molecular Targeted Therapy - methods Mutation Neoplasms - genetics Neoplasms - metabolism Neoplasms - pathology Oncogenes Ovarian cancer Physiological aspects Prognosis Proteins Survival Rate Transforming growth factors Tumors |
title | An Integrative Pan-Cancer Analysis of the Oncogenic Role of COPB2 in Human Tumors |
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