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Physical state & copy number of high risk human papillomavirus type 16 DNA in progression of cervical cancer

BACKGROUND & OBJECTIVES: High-risk human papilloma virus (HR-HPV) infection and its integration in host genome is a key event in malignant transformation of cervical cells. HPV16 being a dominant HR-HPV type, we undertook this study to analyze if viral load and physical state of the virus correl...

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Autores principales: Shukla, Shirish, Mahata, Sutapa, Shishodia, Gauri, Pande, Shailja, Verma, Gaurav, Hedau, Suresh, Bhambhani, Suresh, Kumari, Archana, Batra, Swaraj, Basir, Seemi F., Das, Bhudev C., Bharti, Alok C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078491/
https://www.ncbi.nlm.nih.gov/pubmed/24927339
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author Shukla, Shirish
Mahata, Sutapa
Shishodia, Gauri
Pande, Shailja
Verma, Gaurav
Hedau, Suresh
Bhambhani, Suresh
Kumari, Archana
Batra, Swaraj
Basir, Seemi F.
Das, Bhudev C.
Bharti, Alok C.
author_facet Shukla, Shirish
Mahata, Sutapa
Shishodia, Gauri
Pande, Shailja
Verma, Gaurav
Hedau, Suresh
Bhambhani, Suresh
Kumari, Archana
Batra, Swaraj
Basir, Seemi F.
Das, Bhudev C.
Bharti, Alok C.
author_sort Shukla, Shirish
collection PubMed
description BACKGROUND & OBJECTIVES: High-risk human papilloma virus (HR-HPV) infection and its integration in host genome is a key event in malignant transformation of cervical cells. HPV16 being a dominant HR-HPV type, we undertook this study to analyze if viral load and physical state of the virus correlated with each other in the absence of other confounding variables and examined their potential as predictors of progressive cervical lesions. METHODS: Both, viral load and integration status of HPV16 were determined by real time URR PCR and estimation of E2:E6 ratio in a total of 130 PGMY-RLB -confirmed, monotypic HPV16-infected cervical DNA samples from biopsies of cytology-confirmed low grade (LSIL, 30) and high grade (HSIL, 30), and invasive carcinoma, (squamous cell carcinoma SCC, 70) cases. RESULTS: Investigation of DNA samples revealed a gradual increase in HPV16 viral load over several magnitudes and increased frequency of integration from LSIL to HSIL and HSIL to invasive cancer in relation to the severity of lesions in monotypic HPV16-infected cervical tissues. In a substantial number of precancer (11/60) and cancer cases (29/70), HPV16 was detected in concomitant mixed form. The concomitant form of HPV16 genome carried significantly higher viral load. INTERPRETATION & CONCLUSIONS: Overall, viral load and integration increased with disease severity and could be useful biomarkers in disease progression, at least, in HPV16-infected cervical pre-cancer and cancer lesions.
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spelling pubmed-40784912014-07-02 Physical state & copy number of high risk human papillomavirus type 16 DNA in progression of cervical cancer Shukla, Shirish Mahata, Sutapa Shishodia, Gauri Pande, Shailja Verma, Gaurav Hedau, Suresh Bhambhani, Suresh Kumari, Archana Batra, Swaraj Basir, Seemi F. Das, Bhudev C. Bharti, Alok C. Indian J Med Res Original Article BACKGROUND & OBJECTIVES: High-risk human papilloma virus (HR-HPV) infection and its integration in host genome is a key event in malignant transformation of cervical cells. HPV16 being a dominant HR-HPV type, we undertook this study to analyze if viral load and physical state of the virus correlated with each other in the absence of other confounding variables and examined their potential as predictors of progressive cervical lesions. METHODS: Both, viral load and integration status of HPV16 were determined by real time URR PCR and estimation of E2:E6 ratio in a total of 130 PGMY-RLB -confirmed, monotypic HPV16-infected cervical DNA samples from biopsies of cytology-confirmed low grade (LSIL, 30) and high grade (HSIL, 30), and invasive carcinoma, (squamous cell carcinoma SCC, 70) cases. RESULTS: Investigation of DNA samples revealed a gradual increase in HPV16 viral load over several magnitudes and increased frequency of integration from LSIL to HSIL and HSIL to invasive cancer in relation to the severity of lesions in monotypic HPV16-infected cervical tissues. In a substantial number of precancer (11/60) and cancer cases (29/70), HPV16 was detected in concomitant mixed form. The concomitant form of HPV16 genome carried significantly higher viral load. INTERPRETATION & CONCLUSIONS: Overall, viral load and integration increased with disease severity and could be useful biomarkers in disease progression, at least, in HPV16-infected cervical pre-cancer and cancer lesions. Medknow Publications & Media Pvt Ltd 2014-04 /pmc/articles/PMC4078491/ /pubmed/24927339 Text en Copyright: © Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Shukla, Shirish
Mahata, Sutapa
Shishodia, Gauri
Pande, Shailja
Verma, Gaurav
Hedau, Suresh
Bhambhani, Suresh
Kumari, Archana
Batra, Swaraj
Basir, Seemi F.
Das, Bhudev C.
Bharti, Alok C.
Physical state & copy number of high risk human papillomavirus type 16 DNA in progression of cervical cancer
title Physical state & copy number of high risk human papillomavirus type 16 DNA in progression of cervical cancer
title_full Physical state & copy number of high risk human papillomavirus type 16 DNA in progression of cervical cancer
title_fullStr Physical state & copy number of high risk human papillomavirus type 16 DNA in progression of cervical cancer
title_full_unstemmed Physical state & copy number of high risk human papillomavirus type 16 DNA in progression of cervical cancer
title_short Physical state & copy number of high risk human papillomavirus type 16 DNA in progression of cervical cancer
title_sort physical state & copy number of high risk human papillomavirus type 16 dna in progression of cervical cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078491/
https://www.ncbi.nlm.nih.gov/pubmed/24927339
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