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Increased expression of HPV-E7 oncoprotein correlates with a reduced level of pRb proteins via high viral load in cervical cancer

Human Papillomavirus (HPV) is the most common cause of sexually transmitted diseases and causes a wide range of pathologies including cervical carcinoma. Integration of the HR-HPV DNA into the host genome plays a crucial role in cervical carcinoma. An alteration of the pRb pathways by the E7 protein...

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Autores principales: Mir, Bilal Ahmad, Ahmad, Arif, Farooq, Nighat, Priya, M. Vishnu, Siddiqui, A. H., Asif, M., Manzoor, Rouquia, Ishqi, Hassan Mubarak, Alomar, Suliman Y., Rahaman, P. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497568/
https://www.ncbi.nlm.nih.gov/pubmed/37699974
http://dx.doi.org/10.1038/s41598-023-42022-3
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author Mir, Bilal Ahmad
Ahmad, Arif
Farooq, Nighat
Priya, M. Vishnu
Siddiqui, A. H.
Asif, M.
Manzoor, Rouquia
Ishqi, Hassan Mubarak
Alomar, Suliman Y.
Rahaman, P. F.
author_facet Mir, Bilal Ahmad
Ahmad, Arif
Farooq, Nighat
Priya, M. Vishnu
Siddiqui, A. H.
Asif, M.
Manzoor, Rouquia
Ishqi, Hassan Mubarak
Alomar, Suliman Y.
Rahaman, P. F.
author_sort Mir, Bilal Ahmad
collection PubMed
description Human Papillomavirus (HPV) is the most common cause of sexually transmitted diseases and causes a wide range of pathologies including cervical carcinoma. Integration of the HR-HPV DNA into the host genome plays a crucial role in cervical carcinoma. An alteration of the pRb pathways by the E7 proteins is one of the mechanisms that’s account for the transforming capacity of high-risk papillomavirus. For the proper understanding of the underline mechanism of the progression of the disease, the present study investigate the correlation of concentration of host pRb protein, viral E7 oncoprotein and viral load in early and advanced stages of cervical carcinoma. It was found that the viral load in early stages (stage I and II) was less (log(10) transformed mean value 2.6 and 3.0) compared to advanced stages (stage III and IV) (Log(10) transformed value 5.0 and 5.8) having high expression of HPV E7 onco-protein and reduced level of pRb protein, signifying the role of viral load and expression level of E7 oncoprotein in the progression of cervical cancer.
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spelling pubmed-104975682023-09-14 Increased expression of HPV-E7 oncoprotein correlates with a reduced level of pRb proteins via high viral load in cervical cancer Mir, Bilal Ahmad Ahmad, Arif Farooq, Nighat Priya, M. Vishnu Siddiqui, A. H. Asif, M. Manzoor, Rouquia Ishqi, Hassan Mubarak Alomar, Suliman Y. Rahaman, P. F. Sci Rep Article Human Papillomavirus (HPV) is the most common cause of sexually transmitted diseases and causes a wide range of pathologies including cervical carcinoma. Integration of the HR-HPV DNA into the host genome plays a crucial role in cervical carcinoma. An alteration of the pRb pathways by the E7 proteins is one of the mechanisms that’s account for the transforming capacity of high-risk papillomavirus. For the proper understanding of the underline mechanism of the progression of the disease, the present study investigate the correlation of concentration of host pRb protein, viral E7 oncoprotein and viral load in early and advanced stages of cervical carcinoma. It was found that the viral load in early stages (stage I and II) was less (log(10) transformed mean value 2.6 and 3.0) compared to advanced stages (stage III and IV) (Log(10) transformed value 5.0 and 5.8) having high expression of HPV E7 onco-protein and reduced level of pRb protein, signifying the role of viral load and expression level of E7 oncoprotein in the progression of cervical cancer. Nature Publishing Group UK 2023-09-12 /pmc/articles/PMC10497568/ /pubmed/37699974 http://dx.doi.org/10.1038/s41598-023-42022-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Mir, Bilal Ahmad
Ahmad, Arif
Farooq, Nighat
Priya, M. Vishnu
Siddiqui, A. H.
Asif, M.
Manzoor, Rouquia
Ishqi, Hassan Mubarak
Alomar, Suliman Y.
Rahaman, P. F.
Increased expression of HPV-E7 oncoprotein correlates with a reduced level of pRb proteins via high viral load in cervical cancer
title Increased expression of HPV-E7 oncoprotein correlates with a reduced level of pRb proteins via high viral load in cervical cancer
title_full Increased expression of HPV-E7 oncoprotein correlates with a reduced level of pRb proteins via high viral load in cervical cancer
title_fullStr Increased expression of HPV-E7 oncoprotein correlates with a reduced level of pRb proteins via high viral load in cervical cancer
title_full_unstemmed Increased expression of HPV-E7 oncoprotein correlates with a reduced level of pRb proteins via high viral load in cervical cancer
title_short Increased expression of HPV-E7 oncoprotein correlates with a reduced level of pRb proteins via high viral load in cervical cancer
title_sort increased expression of hpv-e7 oncoprotein correlates with a reduced level of prb proteins via high viral load in cervical cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497568/
https://www.ncbi.nlm.nih.gov/pubmed/37699974
http://dx.doi.org/10.1038/s41598-023-42022-3
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