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RIPOR2 Expression Decreased by HPV-16 E6 and E7 Oncoproteins: An Opportunity in the Search for Prognostic Biomarkers in Cervical Cancer

High-risk human papillomavirus (HPV) infection is the main risk factor for cervical cancer (CC) development, where the continuous expression of E6 and E7 oncoproteins maintain the malignant phenotype. In Mexico, around 70% of CC cases are diagnosed in advanced stages, impacting the survival of patie...

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Autores principales: Olmedo-Nieva, Leslie, Muñoz-Bello, J. Omar, Martínez-Ramírez, Imelda, Martínez-Gutiérrez, Antonio Daniel, Ortiz-Pedraza, Yunuen, González-Espinosa, Claudia, Madrid-Marina, Vicente, Torres-Poveda, Kirvis, Bahena-Roman, Margarita, Lizano, Marcela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740487/
https://www.ncbi.nlm.nih.gov/pubmed/36497200
http://dx.doi.org/10.3390/cells11233942
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author Olmedo-Nieva, Leslie
Muñoz-Bello, J. Omar
Martínez-Ramírez, Imelda
Martínez-Gutiérrez, Antonio Daniel
Ortiz-Pedraza, Yunuen
González-Espinosa, Claudia
Madrid-Marina, Vicente
Torres-Poveda, Kirvis
Bahena-Roman, Margarita
Lizano, Marcela
author_facet Olmedo-Nieva, Leslie
Muñoz-Bello, J. Omar
Martínez-Ramírez, Imelda
Martínez-Gutiérrez, Antonio Daniel
Ortiz-Pedraza, Yunuen
González-Espinosa, Claudia
Madrid-Marina, Vicente
Torres-Poveda, Kirvis
Bahena-Roman, Margarita
Lizano, Marcela
author_sort Olmedo-Nieva, Leslie
collection PubMed
description High-risk human papillomavirus (HPV) infection is the main risk factor for cervical cancer (CC) development, where the continuous expression of E6 and E7 oncoproteins maintain the malignant phenotype. In Mexico, around 70% of CC cases are diagnosed in advanced stages, impacting the survival of patients. The aim of this work was to identify biomarkers affected by HPV-16 E6 and E7 oncoproteins that impact the prognosis of CC patients. Expression profiles dependent on E6 and E7 oncoproteins, as well as their relationship with biological processes and cellular signaling pathways, were analyzed in CC cells. A comparison among expression profiles of E6- and E7-expressing cells and that from a CC cohort obtained from The Cancer Genome Atlas (TCGA) demonstrated that the expression of 13 genes impacts the overall survival (OS). A multivariate analysis revealed that the downregulated expression of RIPOR2 was strongly associated with a worse OS. RIPOR2, including its transcriptional variants, were overwhelmingly depleted in E6- and E7-expressing cells. Finally, in a Mexican cohort, it was found that in premalignant cervical lesions, RIPOR2 expression decreases as the lesions progress; meanwhile, decreased RIPOR2 expression was also associated with a worse OS in CC patients.
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spelling pubmed-97404872022-12-11 RIPOR2 Expression Decreased by HPV-16 E6 and E7 Oncoproteins: An Opportunity in the Search for Prognostic Biomarkers in Cervical Cancer Olmedo-Nieva, Leslie Muñoz-Bello, J. Omar Martínez-Ramírez, Imelda Martínez-Gutiérrez, Antonio Daniel Ortiz-Pedraza, Yunuen González-Espinosa, Claudia Madrid-Marina, Vicente Torres-Poveda, Kirvis Bahena-Roman, Margarita Lizano, Marcela Cells Article High-risk human papillomavirus (HPV) infection is the main risk factor for cervical cancer (CC) development, where the continuous expression of E6 and E7 oncoproteins maintain the malignant phenotype. In Mexico, around 70% of CC cases are diagnosed in advanced stages, impacting the survival of patients. The aim of this work was to identify biomarkers affected by HPV-16 E6 and E7 oncoproteins that impact the prognosis of CC patients. Expression profiles dependent on E6 and E7 oncoproteins, as well as their relationship with biological processes and cellular signaling pathways, were analyzed in CC cells. A comparison among expression profiles of E6- and E7-expressing cells and that from a CC cohort obtained from The Cancer Genome Atlas (TCGA) demonstrated that the expression of 13 genes impacts the overall survival (OS). A multivariate analysis revealed that the downregulated expression of RIPOR2 was strongly associated with a worse OS. RIPOR2, including its transcriptional variants, were overwhelmingly depleted in E6- and E7-expressing cells. Finally, in a Mexican cohort, it was found that in premalignant cervical lesions, RIPOR2 expression decreases as the lesions progress; meanwhile, decreased RIPOR2 expression was also associated with a worse OS in CC patients. MDPI 2022-12-06 /pmc/articles/PMC9740487/ /pubmed/36497200 http://dx.doi.org/10.3390/cells11233942 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Olmedo-Nieva, Leslie
Muñoz-Bello, J. Omar
Martínez-Ramírez, Imelda
Martínez-Gutiérrez, Antonio Daniel
Ortiz-Pedraza, Yunuen
González-Espinosa, Claudia
Madrid-Marina, Vicente
Torres-Poveda, Kirvis
Bahena-Roman, Margarita
Lizano, Marcela
RIPOR2 Expression Decreased by HPV-16 E6 and E7 Oncoproteins: An Opportunity in the Search for Prognostic Biomarkers in Cervical Cancer
title RIPOR2 Expression Decreased by HPV-16 E6 and E7 Oncoproteins: An Opportunity in the Search for Prognostic Biomarkers in Cervical Cancer
title_full RIPOR2 Expression Decreased by HPV-16 E6 and E7 Oncoproteins: An Opportunity in the Search for Prognostic Biomarkers in Cervical Cancer
title_fullStr RIPOR2 Expression Decreased by HPV-16 E6 and E7 Oncoproteins: An Opportunity in the Search for Prognostic Biomarkers in Cervical Cancer
title_full_unstemmed RIPOR2 Expression Decreased by HPV-16 E6 and E7 Oncoproteins: An Opportunity in the Search for Prognostic Biomarkers in Cervical Cancer
title_short RIPOR2 Expression Decreased by HPV-16 E6 and E7 Oncoproteins: An Opportunity in the Search for Prognostic Biomarkers in Cervical Cancer
title_sort ripor2 expression decreased by hpv-16 e6 and e7 oncoproteins: an opportunity in the search for prognostic biomarkers in cervical cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740487/
https://www.ncbi.nlm.nih.gov/pubmed/36497200
http://dx.doi.org/10.3390/cells11233942
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