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Identification of key pseudogenes in nasopharyngeal carcinoma based on RNA-Seq analysis

BACKGROUND: Nasopharyngeal carcinoma (NPC) is a malignant head and neck tumor, and more than 70% of new cases are in East and Southeast Asia. However, association between NPC and pseudogenes playing important roles in genesis of multiple tumor types is still not clear and needs to be investigated. M...

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Autores principales: Zhang, Xiujuan, Song, Xiaole, Lai, Yuting, Zhu, Bijun, Luo, Jiqin, Yu, Hongmeng, Yu, Yiqun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088053/
https://www.ncbi.nlm.nih.gov/pubmed/33931030
http://dx.doi.org/10.1186/s12885-021-08211-x
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author Zhang, Xiujuan
Song, Xiaole
Lai, Yuting
Zhu, Bijun
Luo, Jiqin
Yu, Hongmeng
Yu, Yiqun
author_facet Zhang, Xiujuan
Song, Xiaole
Lai, Yuting
Zhu, Bijun
Luo, Jiqin
Yu, Hongmeng
Yu, Yiqun
author_sort Zhang, Xiujuan
collection PubMed
description BACKGROUND: Nasopharyngeal carcinoma (NPC) is a malignant head and neck tumor, and more than 70% of new cases are in East and Southeast Asia. However, association between NPC and pseudogenes playing important roles in genesis of multiple tumor types is still not clear and needs to be investigated. METHODS: Using RNA-Sequencing (RNA-seq) technology, we analyzed pseudogene expression in 13 primary NPC and 6 recurrent NPC samples as well as their paracancerous counterparts. Quantitative PCR was used to validate the differentially expressed pseudogenes. RESULTS: We found 251 differentially expressed pseudogenes including 73 up-regulated and 178 down-regulated ones between primary NPC and paracancerous tissues. Enrichment analysis of gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway were conducted to filter out the key pseudogenes. We reported that pseudogenes from cytochrome P450 (CYP) family, such as CYP2F2P, CYP2G1P, CYP4F24P, CYP2B7P and CYP2G2P were significantly down-regulated in NPC compared to paracancerous tissues, while IGHV1OR15–2, IGHV3–11, FCGR1CP and IGHV3–69-1 belonging to Fc gamma receptors were significantly up-regulated. CYP2B7P, CYP2F2P and CYP4F26P were enriched in arachidonic acid metabolism pathway. The qRT-PCR analysis validated the lower expression of pseudogenes CYP2F2P and CYP2B7P in NPC tissues and cell lines compared to paracancerous tissues and normal human nasopharyngeal epithelial cell line. CYP2B7P overexpression weakened migratory and invasive capacity of NPC cell line. Moreover, the expression pattern of those pseudogenes in recurrent NPC tissues was different from the primary NPC. CONCLUSION: This study suggested the role of pseudogenes in tumorigenesis and progression, potentially functioning as therapeutic targets to NPC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-021-08211-x.
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spelling pubmed-80880532021-05-03 Identification of key pseudogenes in nasopharyngeal carcinoma based on RNA-Seq analysis Zhang, Xiujuan Song, Xiaole Lai, Yuting Zhu, Bijun Luo, Jiqin Yu, Hongmeng Yu, Yiqun BMC Cancer Research BACKGROUND: Nasopharyngeal carcinoma (NPC) is a malignant head and neck tumor, and more than 70% of new cases are in East and Southeast Asia. However, association between NPC and pseudogenes playing important roles in genesis of multiple tumor types is still not clear and needs to be investigated. METHODS: Using RNA-Sequencing (RNA-seq) technology, we analyzed pseudogene expression in 13 primary NPC and 6 recurrent NPC samples as well as their paracancerous counterparts. Quantitative PCR was used to validate the differentially expressed pseudogenes. RESULTS: We found 251 differentially expressed pseudogenes including 73 up-regulated and 178 down-regulated ones between primary NPC and paracancerous tissues. Enrichment analysis of gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway were conducted to filter out the key pseudogenes. We reported that pseudogenes from cytochrome P450 (CYP) family, such as CYP2F2P, CYP2G1P, CYP4F24P, CYP2B7P and CYP2G2P were significantly down-regulated in NPC compared to paracancerous tissues, while IGHV1OR15–2, IGHV3–11, FCGR1CP and IGHV3–69-1 belonging to Fc gamma receptors were significantly up-regulated. CYP2B7P, CYP2F2P and CYP4F26P were enriched in arachidonic acid metabolism pathway. The qRT-PCR analysis validated the lower expression of pseudogenes CYP2F2P and CYP2B7P in NPC tissues and cell lines compared to paracancerous tissues and normal human nasopharyngeal epithelial cell line. CYP2B7P overexpression weakened migratory and invasive capacity of NPC cell line. Moreover, the expression pattern of those pseudogenes in recurrent NPC tissues was different from the primary NPC. CONCLUSION: This study suggested the role of pseudogenes in tumorigenesis and progression, potentially functioning as therapeutic targets to NPC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-021-08211-x. BioMed Central 2021-04-30 /pmc/articles/PMC8088053/ /pubmed/33931030 http://dx.doi.org/10.1186/s12885-021-08211-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhang, Xiujuan
Song, Xiaole
Lai, Yuting
Zhu, Bijun
Luo, Jiqin
Yu, Hongmeng
Yu, Yiqun
Identification of key pseudogenes in nasopharyngeal carcinoma based on RNA-Seq analysis
title Identification of key pseudogenes in nasopharyngeal carcinoma based on RNA-Seq analysis
title_full Identification of key pseudogenes in nasopharyngeal carcinoma based on RNA-Seq analysis
title_fullStr Identification of key pseudogenes in nasopharyngeal carcinoma based on RNA-Seq analysis
title_full_unstemmed Identification of key pseudogenes in nasopharyngeal carcinoma based on RNA-Seq analysis
title_short Identification of key pseudogenes in nasopharyngeal carcinoma based on RNA-Seq analysis
title_sort identification of key pseudogenes in nasopharyngeal carcinoma based on rna-seq analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088053/
https://www.ncbi.nlm.nih.gov/pubmed/33931030
http://dx.doi.org/10.1186/s12885-021-08211-x
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