Type-dependent E6/E7 mRNA expression of single and multiple high-risk human papillomavirus infections in cervical neoplasia

IF 3.4 3区 医学 Q2 VIROLOGY Journal of Clinical Virology Pub Date : 2012-05-01 DOI:10.1016/j.jcv.2012.01.012
Elin Andersson , Cecilia Kärrberg , Thomas Rådberg , Lennart Blomqvist , Britt-Marie Zetterqvist , Walter Ryd , Magnus Lindh , Peter Horal
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引用次数: 16

Abstract

Background

Coinfection with multiple HPV types is common in cervical lesions, but the biological significance of the individual infections is difficult to establish. Expression of oncogenic E6/E7 HPV mRNA is correlated to risk of malignant progression, commercial assays for genotyping E6/E7 mRNA of all HR-HPV are lacking.

Objectives

To characterize the tendency of 12 HR-HPV to express mRNA, correlated to the severity of the cervical lesion. Furthermore, we wanted to analyse mRNA expression in multiple infections, in order to establish which genotype may be responsible for cellular transformation.

Study design

245 samples from women with normal histology, various grades of dysplasia (cervical intraepithelial neoplasia grade 1–3), and cancer, were analysed for presence and genotyping of HPV DNA and mRNA using an in house real-time PCR test.

Results

Presence of mRNA was detected for 64% of the in total 422 HPV infections present in the samples, and more commonly in high-grade lesions. In 88% of DNA-positive samples from CIN2+ lesions, mRNA could be detected, compared to 33% of DNA-positive samples from women in screening with normal cytology. The genotype most prone to express mRNA in high-grade lesions was HPV45, followed by HPV16 and HPV31, less prone was HPV59. Expression of mRNA was significantly enhanced in CIN2+ lesions, an association also found for HPV16. In 52% of multiple infections (in which mRNA expression was generally more common), more than one genotype expressed mRNA, a phenomenon increasing with severity of lesion. Presence of mRNA could more often be detected in samples with multiple infections than in samples with single infections.

Conclusions

The frequent expression of E6/E7 by HPV45 may promote oncogenicity and could be of clinical importance. Since presence of E6/E7 mRNA was common in multiple infections regardless of histology, multiple infection could be a clinically important finding. In multiple HPV infections, mRNA testing may identify the genotype that causes transformation. However, since mRNA expression of several genotypes in one sample is common, further and larger studies using complementary techniques are required.

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宫颈肿瘤中单一和多重高危人乳头瘤病毒感染的E6/E7 mRNA表达
背景多种HPV型别合并感染在宫颈病变中很常见,但个体感染的生物学意义难以确定。致癌性E6/E7 HPV mRNA的表达与恶性进展的风险相关,缺乏所有HR-HPV的E6/E7 mRNA基因分型的商业分析。目的探讨宫颈病变严重程度与12种HR-HPV mRNA表达的关系。此外,我们希望分析多种感染中的mRNA表达,以确定哪种基因型可能负责细胞转化。研究设计:采用室内实时PCR检测,对245例组织学正常、不同级别的不典型增生(宫颈上皮内瘤变1-3级)和癌症的女性样本进行HPV DNA和mRNA的存在和基因分型分析。结果在422例HPV感染中,有64%的人检测到mRNA的存在,在高级别病变中更为常见。在来自CIN2+病变的dna阳性样本中,88%可以检测到mRNA,而在正常细胞学筛查中,来自女性的dna阳性样本中,这一比例为33%。高级别病变中最易表达mRNA的基因型为HPV45,其次为HPV16和HPV31, HPV59的表达率较低。mRNA的表达在CIN2+病变中显著增强,与HPV16也有关联。在52%的多重感染(mRNA表达普遍更为常见)中,不止一种基因型表达mRNA,这一现象随着病变严重程度的增加而增加。在多次感染的样本中,mRNA的存在比在单次感染的样本中更常被检测到。结论HPV45频繁表达E6/E7可能促进肿瘤的发生,具有重要的临床意义。由于E6/E7 mRNA的存在在多重感染中是常见的,无论组织学如何,多重感染可能是一个重要的临床发现。在多种HPV感染中,mRNA检测可以确定导致转化的基因型。然而,由于一个样本中几种基因型的mRNA表达是常见的,因此需要使用互补技术进行进一步和更大规模的研究。
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来源期刊
Journal of Clinical Virology
Journal of Clinical Virology 医学-病毒学
CiteScore
22.70
自引率
1.10%
发文量
149
审稿时长
24 days
期刊介绍: The Journal of Clinical Virology, an esteemed international publication, serves as the official journal for both the Pan American Society for Clinical Virology and The European Society for Clinical Virology. Dedicated to advancing the understanding of human virology in clinical settings, the Journal of Clinical Virology focuses on disseminating research papers and reviews pertaining to the clinical aspects of virology. Its scope encompasses articles discussing diagnostic methodologies and virus-induced clinical conditions, with an emphasis on practicality and relevance to clinical practice. The journal publishes on topics that include: • new diagnostic technologies • nucleic acid amplification and serologic testing • targeted and metagenomic next-generation sequencing • emerging pandemic viral threats • respiratory viruses • transplant viruses • chronic viral infections • cancer-associated viruses • gastrointestinal viruses • central nervous system viruses • one health (excludes animal health)
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