Transcriptomic analysis provides insight into the mechanism of IKKβ-mediated suppression of HPV18E6-induced cellular abnormalities

AbstractHigh-risk human papillomaviruses (HPVs) 16 and 18 are responsible for more than 70% of cervical cancers and majority of other HPV-associated cancers world-wide. Current treatments for these cancers have limited efficacy, which in turn has resulted in disease recurrence and po...

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Main Authors: Quincy P Collins, Michael J Grunsted, Dahiana Arcila, Yi Xiong, Mojgan Padash Barmchi
Format: Article
Language:English
Published: Oxford University Press 2023-02-01
Series:G3: Genes, Genomes, Genetics
Online Access:https://academic.oup.com/g3journal/article-lookup/doi/10.1093/g3journal/jkad020
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author Quincy P Collins
Michael J Grunsted
Dahiana Arcila
Yi Xiong
Mojgan Padash Barmchi
author_facet Quincy P Collins
Michael J Grunsted
Dahiana Arcila
Yi Xiong
Mojgan Padash Barmchi
author_sort Quincy P Collins
collection DOAJ
description AbstractHigh-risk human papillomaviruses (HPVs) 16 and 18 are responsible for more than 70% of cervical cancers and majority of other HPV-associated cancers world-wide. Current treatments for these cancers have limited efficacy, which in turn has resulted in disease recurrence and poor survival rates in advanced disease stages. Hence, there is a significant need for development of novel molecularly-targeted therapeutics. This can only be achieved through improved understanding of disease mechanism. Recently, we developed a Drosophila
first_indexed 2024-03-13T01:43:00Z
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institution Directory Open Access Journal
issn 2160-1836
language English
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spelling doaj.art-a8006480ff5147c581fd924f5c30c6142023-07-03T11:12:58ZengOxford University PressG3: Genes, Genomes, Genetics2160-18362023-02-0113410.1093/g3journal/jkad020Transcriptomic analysis provides insight into the mechanism of IKKβ-mediated suppression of HPV18E6-induced cellular abnormalitiesQuincy P Collins0Michael J Grunsted1Dahiana Arcila2Yi Xiong3Mojgan Padash Barmchi4Department of Biology, University of Oklahoma, Norman, OK 73019, USADepartment of Biology, University of Oklahoma, Norman, OK 73019, USADepartment of Biology, University of Oklahoma, Norman, OK 73019, USADepartment of Microbiology and Plant Biology, University of Oklahoma, Norman, OK 73019, USADepartment of Biology, University of Oklahoma, Norman, OK 73019, USA AbstractHigh-risk human papillomaviruses (HPVs) 16 and 18 are responsible for more than 70% of cervical cancers and majority of other HPV-associated cancers world-wide. Current treatments for these cancers have limited efficacy, which in turn has resulted in disease recurrence and poor survival rates in advanced disease stages. Hence, there is a significant need for development of novel molecularly-targeted therapeutics. This can only be achieved through improved understanding of disease mechanism. Recently, we developed a Drosophilahttps://academic.oup.com/g3journal/article-lookup/doi/10.1093/g3journal/jkad020
spellingShingle Quincy P Collins
Michael J Grunsted
Dahiana Arcila
Yi Xiong
Mojgan Padash Barmchi
Transcriptomic analysis provides insight into the mechanism of IKKβ-mediated suppression of HPV18E6-induced cellular abnormalities
G3: Genes, Genomes, Genetics
title Transcriptomic analysis provides insight into the mechanism of IKKβ-mediated suppression of HPV18E6-induced cellular abnormalities
title_full Transcriptomic analysis provides insight into the mechanism of IKKβ-mediated suppression of HPV18E6-induced cellular abnormalities
title_fullStr Transcriptomic analysis provides insight into the mechanism of IKKβ-mediated suppression of HPV18E6-induced cellular abnormalities
title_full_unstemmed Transcriptomic analysis provides insight into the mechanism of IKKβ-mediated suppression of HPV18E6-induced cellular abnormalities
title_short Transcriptomic analysis provides insight into the mechanism of IKKβ-mediated suppression of HPV18E6-induced cellular abnormalities
title_sort transcriptomic analysis provides insight into the mechanism of ikkβ mediated suppression of hpv18e6 induced cellular abnormalities
url https://academic.oup.com/g3journal/article-lookup/doi/10.1093/g3journal/jkad020
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