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Updated: Apr 1, 2026

RNAscope for In situ Detection of Transcriptionally Active Human Papillomavirus in Head and Neck Squamous Cell Carcinoma
Published on: March 11, 2014
[Detection of microRNAs seed sequences within human papillomavirus genomes]
David Pineda-Gómez1, Efraín Garrido, Pedro Chávez
1Unidad de Investigación Médica en Enfermedades Oncológicas, Hospital de Oncología, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Distrito Federal, México. maosal89@yahoo.com.
Abstract:
In this paper we are reporting for the first time the presence of seed sequences of human and viral microRNAs embedded within both high and low risk human papillomavirus (HPV) genomes. These seed sequences have high oncogenic potential. They were found using an in silico analysis based on the microRNA sequences added to Sanger's database. Among these sequences, it was observed a potential fingerprint harbouring several repeated sequences of microRNA 297 (miR-297) within the LCR region of HPV types 16, 18, 33, 45 and 52. Further analyses were performed for low risk HPV types 6 and 11 and we observed that the probable fingerprint was absent in HPV11, even when we detected other repeated sequences of miR-363. According to these findings, besides the fact that we detected the presence of microRNA sequences within HPV genomes, we suggest a common putative viral mechanism of gene expression regulation shared among human virus.
Insights
This study discovered human and viral microRNA seed sequences within high and low-risk human papillomavirus (HPV) genomes, suggesting a shared viral gene regulation mechanism. These oncogenic sequences were identified using in silico analysis.
Area of Science:
- Virology
- Molecular Biology
- Genomics
Background:
- Human papillomavirus (HPV) is a common viral infection linked to cancer.
- MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression.
- The presence and role of viral miRNAs within HPV genomes remain incompletely understood.
Purpose of the Study:
- To investigate the presence of human and viral microRNA seed sequences within high and low-risk HPV genomes.
- To identify potential oncogenic microRNA sequences and their genomic locations.
- To explore a potential common viral mechanism for gene expression regulation.
Main Methods:
- In silico analysis of HPV genomes (high-risk types 16, 18, 33, 45, 52 and low-risk types 6, 11).
- Utilized microRNA sequences from Sanger's database for comparison.
- Focused on identifying seed sequences and specific microRNA fingerprints, particularly miR-297 and miR-363.
Main Results:
- Detected seed sequences of human and viral microRNAs in both high and low-risk HPV genomes.
- Identified a potential fingerprint with repeated miR-297 sequences in the LCR region of several high-risk HPV types.
- Observed absence of the miR-297 fingerprint in HPV11, though other sequences like miR-363 were present.
Conclusions:
- HPV genomes harbor microRNA sequences with high oncogenic potential.
- A specific miR-297 fingerprint in high-risk HPV types suggests a targeted viral mechanism.
- These findings point towards a conserved, putative viral mechanism for gene expression regulation across different human viruses.
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