Suppr超能文献

在宫颈细胞学和组织学正常及低度病变的女性中可检测到的高拷贝HPV16的早期整合。

Early integration of high copy HPV16 detectable in women with normal and low grade cervical cytology and histology.

作者信息

Kulmala S-M A, Syrjänen S M, Gyllensten U B, Shabalova I P, Petrovichev N, Tosi P, Syrjänen K J, Johansson B C

机构信息

Department of Oral Pathology, Institute of Dentistry, University of Turku, Finland.

出版信息

J Clin Pathol. 2006 May;59(5):513-7. doi: 10.1136/jcp.2004.024570. Epub 2006 Feb 16.

Abstract

BACKGROUND

Integration of human papillomavirus (HPV) DNA has been considered a late event in cervical carcinogenesis. However, integrated forms of HPV were recently detected in cancer precursor lesions using a new real time polymerase chain reaction (PCR) to detect the deletions at the 3362-3443 region of HPV16 E2 OBJECTIVE: To study the frequency of HPV16 DNA integration in cervical lesions and compare the sensitivity of an additional upstream region of the E2 ORF (2962-3138) in detecting HPV integration.

METHODS

Using the TaqMan based PCR, HPV16 positive DNA samples were analysed in 164 cervical scrapings from women participating in a multicentre screening trial. Biopsy confirmation was available in 62 cases.

RESULTS

Primers targeting the 3362-3443 region detected the majority of E2 deletions. In only 23% of the samples was the E2 upstream region equal or better target than the 3362-3443 region. Mixed (episomal/integrated) pattern was the most prevalent physical state of HPV16, also present in PAP smears with normal morphology. Pure integrated form was most prevalent in HSIL and cancer lesions, but also detectable in low grade abnormalities (NSIL, ASC-US, LSIL). Women with only integrated HPV16 were almost 10 years older than those with episomal HPV16. Viral load of integrated HPV16 was related to cytological abnormality (p = 0.003) but not to histology.

CONCLUSIONS

Integrated HPV16 is present in low grade cervical lesions, mostly mixed with the episomal form. Women with the pure integrated form of HPV16 are older than those with the other forms.

摘要

背景

人乳头瘤病毒(HPV)DNA整合被认为是宫颈癌发生过程中的晚期事件。然而,最近使用一种新的实时聚合酶链反应(PCR)在癌前病变中检测到了HPV的整合形式,该方法用于检测HPV16 E2基因3362 - 3443区域的缺失。目的:研究宫颈病变中HPV16 DNA整合的频率,并比较E2开放阅读框(ORF)另一个上游区域(2962 - 3138)在检测HPV整合方面的敏感性。

方法

使用基于TaqMan的PCR,对参与多中心筛查试验的164名女性的宫颈刮片进行HPV16阳性DNA样本分析。62例有活检确诊结果。

结果

靶向3362 - 3443区域的引物检测到了大多数E2缺失。仅23%的样本中,E2上游区域作为靶点与3362 - 3443区域相当或更好。混合(游离/整合)模式是HPV16最普遍的物理状态,在形态正常的巴氏涂片样本中也存在。纯整合形式在高级别鳞状上皮内病变(HSIL)和癌性病变中最普遍,但在低级别异常(非典型鳞状细胞不能明确意义,ASC-US;低级别鳞状上皮内病变,LSIL)中也可检测到。仅携带整合型HPV16的女性比携带游离型HPV16的女性年龄大近10岁。整合型HPV16的病毒载量与细胞学异常相关(p = 0.003),但与组织学无关。

结论

整合型HPV16存在于低级别宫颈病变中,大多与游离形式混合存在。携带纯整合型HPV16的女性比携带其他形式的女性年龄大。

相似文献

1
Early integration of high copy HPV16 detectable in women with normal and low grade cervical cytology and histology.
J Clin Pathol. 2006 May;59(5):513-7. doi: 10.1136/jcp.2004.024570. Epub 2006 Feb 16.
2
Viral DNA load, physical status and E2/E6 ratio as markers to grade HPV16 positive women for high-grade cervical lesions.
Gynecol Oncol. 2007 Sep;106(3):549-57. doi: 10.1016/j.ygyno.2007.05.004. Epub 2007 Jun 13.
5
Viral E6 is overexpressed via high viral load in invasive cervical cancer with episomal HPV16.
BMC Cancer. 2017 Feb 15;17(1):136. doi: 10.1186/s12885-017-3124-9.
6
Physical and methylation status of human papillomavirus 16 in asymptomatic cervical infections changes with malignant transformation.
J Clin Pathol. 2015 Mar;68(3):206-11. doi: 10.1136/jclinpath-2014-202611. Epub 2015 Jan 6.
7
The physical state of HPV16 infection and its clinical significance in cancer precursor lesion and cervical carcinoma.
J Cancer Res Clin Oncol. 2008 Dec;134(12):1355-61. doi: 10.1007/s00432-008-0413-3. Epub 2008 May 14.

引用本文的文献

2
The Hallmarks of Cervical Cancer: Molecular Mechanisms Induced by Human Papillomavirus.
Biology (Basel). 2024 Jan 27;13(2):77. doi: 10.3390/biology13020077.
3
4
5
Insight into Oncogenic Viral Pathways as Drivers of Viral Cancers: Implication for Effective Therapy.
Curr Oncol. 2023 Feb 5;30(2):1924-1944. doi: 10.3390/curroncol30020150.
8
Biology of HPV Mediated Carcinogenesis and Tumor Progression.
Semin Radiat Oncol. 2021 Oct;31(4):265-273. doi: 10.1016/j.semradonc.2021.02.006.
9
HPV-16 E2/E6 and POU5F1B as Biomarkers to Determine Cervical High-Grade Squamous Lesions and More.
J Inflamm Res. 2020 Oct 29;13:813-821. doi: 10.2147/JIR.S278911. eCollection 2020.

本文引用的文献

6
HPV 16 detection in cervical lesions, physical state of viral DNA and changes in p53 gene.
Sao Paulo Med J. 2003 Mar 5;121(2):67-71. doi: 10.1590/s1516-31802003000200007. Epub 2003 Jul 14.
8
Study of viral integration of HPV-16 in young patients with LSIL.
J Clin Pathol. 2003 Jul;56(7):532-6. doi: 10.1136/jcp.56.7.532.
9
Epidemiologic classification of human papillomavirus types associated with cervical cancer.
N Engl J Med. 2003 Feb 6;348(6):518-27. doi: 10.1056/NEJMoa021641.
10
Viral load of HPV in esophageal squamous cell carcinoma.
Int J Cancer. 2003 Feb 10;103(4):496-500. doi: 10.1002/ijc.10865.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验