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Persistent High-Risk HPV Infection and Molecular Changes Related to the Development of Cervical Cancer
This article is a preliminary investigational study that is aimed at giving hints about the interesting biomarkers involved in the transition process from low-grade cervix lesion to invasive cervical cancer. Our study focuses on the risk factors and tumour molecular changes in one patient. First in...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7845664/ https://www.ncbi.nlm.nih.gov/pubmed/33552605 http://dx.doi.org/10.1155/2020/6806857 |
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author | Moreno-Acosta, Pablo Romero-Rojas, Alfredo Vial, Nicolas Huertas, Antonio Acosta, Jinneth Mayorga, Diana Carrillo, Schyrly Molano, Monica Gamboa, Oscar Cotes, Martha Casadiego, Camila Vallard, Alexis Magne, Nicolas |
author_facet | Moreno-Acosta, Pablo Romero-Rojas, Alfredo Vial, Nicolas Huertas, Antonio Acosta, Jinneth Mayorga, Diana Carrillo, Schyrly Molano, Monica Gamboa, Oscar Cotes, Martha Casadiego, Camila Vallard, Alexis Magne, Nicolas |
author_sort | Moreno-Acosta, Pablo |
collection | PubMed |
description | This article is a preliminary investigational study that is aimed at giving hints about the interesting biomarkers involved in the transition process from low-grade cervix lesion to invasive cervical cancer. Our study focuses on the risk factors and tumour molecular changes in one patient. First in 1986, she was diagnosed a preinvasive cervix lesion. Then, 16 years later, she was diagnosed an invasive cervical cancer. The 2002 diagnosis was a squamous cell carcinoma of the cervix, stage IIIB (FIGO), whereas in 1986, she had been diagnosed a high-grade squamous intraepithelial cervical lesion. Retrospectively, the analysis of samples of preneoplastic lesions and invasive cervical cancer confirmed the histopathological diagnoses and detected the presence of HPV type and HPV-16 variants, as well as the overexpression of proteins such as hTERT, IGF1Rα, IGF1Rβ, CAIX, and GLUT1. Finally, the Arg72Pro polymorphism was detected in TP53. The role of high-risk HPV and HPV-16 variants and of hTERT, IGF1Rα, IGF1Rβ, CAIX, and GLUT1 variations seemed confirmed in the development and progression of cervical cancer. As a result, analyzing the molecular changes in one and same tumour that progresses from a low-grade cervix lesion to invasive cervical cancer could provide valuable information in order to improve detection, diagnosis, and treatment in the future. |
format | Online Article Text |
id | pubmed-7845664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-78456642021-02-04 Persistent High-Risk HPV Infection and Molecular Changes Related to the Development of Cervical Cancer Moreno-Acosta, Pablo Romero-Rojas, Alfredo Vial, Nicolas Huertas, Antonio Acosta, Jinneth Mayorga, Diana Carrillo, Schyrly Molano, Monica Gamboa, Oscar Cotes, Martha Casadiego, Camila Vallard, Alexis Magne, Nicolas Case Rep Obstet Gynecol Case Report This article is a preliminary investigational study that is aimed at giving hints about the interesting biomarkers involved in the transition process from low-grade cervix lesion to invasive cervical cancer. Our study focuses on the risk factors and tumour molecular changes in one patient. First in 1986, she was diagnosed a preinvasive cervix lesion. Then, 16 years later, she was diagnosed an invasive cervical cancer. The 2002 diagnosis was a squamous cell carcinoma of the cervix, stage IIIB (FIGO), whereas in 1986, she had been diagnosed a high-grade squamous intraepithelial cervical lesion. Retrospectively, the analysis of samples of preneoplastic lesions and invasive cervical cancer confirmed the histopathological diagnoses and detected the presence of HPV type and HPV-16 variants, as well as the overexpression of proteins such as hTERT, IGF1Rα, IGF1Rβ, CAIX, and GLUT1. Finally, the Arg72Pro polymorphism was detected in TP53. The role of high-risk HPV and HPV-16 variants and of hTERT, IGF1Rα, IGF1Rβ, CAIX, and GLUT1 variations seemed confirmed in the development and progression of cervical cancer. As a result, analyzing the molecular changes in one and same tumour that progresses from a low-grade cervix lesion to invasive cervical cancer could provide valuable information in order to improve detection, diagnosis, and treatment in the future. Hindawi 2020-07-23 /pmc/articles/PMC7845664/ /pubmed/33552605 http://dx.doi.org/10.1155/2020/6806857 Text en Copyright © 2020 Pablo Moreno-Acosta et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Moreno-Acosta, Pablo Romero-Rojas, Alfredo Vial, Nicolas Huertas, Antonio Acosta, Jinneth Mayorga, Diana Carrillo, Schyrly Molano, Monica Gamboa, Oscar Cotes, Martha Casadiego, Camila Vallard, Alexis Magne, Nicolas Persistent High-Risk HPV Infection and Molecular Changes Related to the Development of Cervical Cancer |
title | Persistent High-Risk HPV Infection and Molecular Changes Related to the Development of Cervical Cancer |
title_full | Persistent High-Risk HPV Infection and Molecular Changes Related to the Development of Cervical Cancer |
title_fullStr | Persistent High-Risk HPV Infection and Molecular Changes Related to the Development of Cervical Cancer |
title_full_unstemmed | Persistent High-Risk HPV Infection and Molecular Changes Related to the Development of Cervical Cancer |
title_short | Persistent High-Risk HPV Infection and Molecular Changes Related to the Development of Cervical Cancer |
title_sort | persistent high-risk hpv infection and molecular changes related to the development of cervical cancer |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7845664/ https://www.ncbi.nlm.nih.gov/pubmed/33552605 http://dx.doi.org/10.1155/2020/6806857 |
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