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LAMP-based electrochemical platform for monitoring HPV genome integration at the mRNA level associated with higher risk of cervical cancer progression
N. Izadi, J. Strmiskova, M. Anton, J. Hausnerova, M. Bartosik
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
Grantová podpora
Ministerstvo Zdravotnictví Ceské Republiky
Ministerstvo Školství, Mládeže a Telovýchovy
Agentura Pro Zdravotnický Výzkum Ceské Republiky
NU21-08-00057
the Czech Health Research Council
LX22NPO5102
National Institute for Cancer Research
LM2023033
the European Union-Next Generation EU
LM2023033
Large research infrastructure BBMRI.cz
00209805
MH CZ-DRO
PubMed
39420658
DOI
10.1002/jmv.70008
Knihovny.cz E-zdroje
- MeSH
- biosenzitivní techniky metody MeSH
- DNA vazebné proteiny genetika MeSH
- DNA virů genetika MeSH
- elektrochemické techniky * metody MeSH
- genom virový MeSH
- infekce papilomavirem * virologie MeSH
- integrace viru * genetika MeSH
- lidé MeSH
- lidský papilomavirus 16 * genetika MeSH
- messenger RNA * genetika MeSH
- nádory děložního čípku * virologie MeSH
- onkogenní proteiny virové * genetika MeSH
- Papillomavirus E7 - proteiny * genetika MeSH
- progrese nemoci MeSH
- RNA virová genetika MeSH
- techniky amplifikace nukleových kyselin metody MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
Human papillomaviruses (HPVs) represent a diverse group of double-stranded DNA viruses associated with various types of cancers, notably cervical cancer. High-risk types of HPVs exhibit their oncogenic potential through the integration of their DNA into the host genome. This integration event contributes significantly to genomic instability and the progression of malignancy. However, traditional detection methods, such as immunohistochemistry or PCR-based assays, face inherent challenges, and thus alternative tools are being developed to fasten and simplify the analysis. Our study introduces an innovative biosensing platform that combines loop-mediated amplification with electrochemical (EC) analysis for the specific detection of HPV16 integration. By targeting key elements like the E7 mRNA, a central player in HPV integration, and the E2 viral gene transcript lost upon integration, we show clear distinction between episomal and integrated forms of HPV16. Our EC data confirmed higher E7 expression in HPV16-positive cell lines having integrated forms of viral genome, while E2 expression was diminished in cells with fully integrated genomes. Moreover, we revealed distinct expression patterns in cervical tissue of patients, correlating well with digital droplet PCR, qRT-PCR, or immunohistochemical staining. Our platform thus offers insights into HPV integration in clinical samples and facilitates further advancements in cervical cancer research and diagnostics.
National Centre for Biomolecular Research Faculty of Science Masaryk University Brno Czech Republic
Research Centre for Applied Molecular Oncology Masaryk Memorial Cancer Institute Brno Czech Republic
Citace poskytuje Crossref.org
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