Study of viral integration of HPV-16 in young patients with LSIL

Aims: To investigate the physical status of human papillomavirus 16 (HPV-16) in low grade squamous intraepithelial lesions (LSILs) as a means of determining the percentage of viral integration. Methods: Ninety two LSIL/HPV positive Thin Prep™ samples were initially tested for the E6 gene by the poly...

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Veröffentlicht in:Journal of clinical pathology 2003-07, Vol.56 (7), p.532-536
Hauptverfasser: Gallo, G, Bibbo, M, Bagella, L, Zamparelli, A, Sanseverino, F, Giovagnoli, M R, Vecchione, A, Giordano, A
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container_end_page 536
container_issue 7
container_start_page 532
container_title Journal of clinical pathology
container_volume 56
creator Gallo, G
Bibbo, M
Bagella, L
Zamparelli, A
Sanseverino, F
Giovagnoli, M R
Vecchione, A
Giordano, A
description Aims: To investigate the physical status of human papillomavirus 16 (HPV-16) in low grade squamous intraepithelial lesions (LSILs) as a means of determining the percentage of viral integration. Methods: Ninety two LSIL/HPV positive Thin Prep™ samples were initially tested for the E6 gene by the polymerase chain reaction (PCR) to identify the HPV-16 virus. To avoid false positive results, the specificity of the bands obtained from PCR was confirmed by Southern blot hybridisation with internal oligonucleotide probes. Next, a PCR screen for the E2 gene was performed to identify those samples in which the virus was integrated. Viral integration was detected in just over half of them. Results: Twenty of the 92 samples were HPV-16 positive, as shown by PCR for the E6 gene. Southern blot analysis confirmed that 13 of these samples were positive for the viral E6 gene. Thus, viral integration was detected in just over a half of the samples positive for HPV-16. Conclusions: These data show that HPV-16 integration occurs in a subset of LSILs. The measurement of HPV-16 integration would be a helpful complementary tool for cytological evaluation in primary cervical screening to identify those patients at risk of developing high grade squamous intraepithelial lesions and cervical cancer.
doi_str_mv 10.1136/jcp.56.7.532
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Methods: Ninety two LSIL/HPV positive Thin Prep™ samples were initially tested for the E6 gene by the polymerase chain reaction (PCR) to identify the HPV-16 virus. To avoid false positive results, the specificity of the bands obtained from PCR was confirmed by Southern blot hybridisation with internal oligonucleotide probes. Next, a PCR screen for the E2 gene was performed to identify those samples in which the virus was integrated. Viral integration was detected in just over half of them. Results: Twenty of the 92 samples were HPV-16 positive, as shown by PCR for the E6 gene. Southern blot analysis confirmed that 13 of these samples were positive for the viral E6 gene. Thus, viral integration was detected in just over a half of the samples positive for HPV-16. Conclusions: These data show that HPV-16 integration occurs in a subset of LSILs. The measurement of HPV-16 integration would be a helpful complementary tool for cytological evaluation in primary cervical screening to identify those patients at risk of developing high grade squamous intraepithelial lesions and cervical cancer.</description><identifier>ISSN: 0021-9746</identifier><identifier>EISSN: 1472-4146</identifier><identifier>DOI: 10.1136/jcp.56.7.532</identifier><identifier>PMID: 12835300</identifier><identifier>CODEN: JCPAAK</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and Association of Clinical Pathologists</publisher><subject>Adult ; Biological and medical sciences ; Carcinoma, Squamous Cell - virology ; Causes of ; Cervical cancer ; Complications and side effects ; DNA, Viral - analysis ; Female ; Female genital diseases ; Genetic aspects ; Genital system. Mammary gland ; Gynecology. Andrology. Obstetrics ; high grade squamous intraepithelial lesion ; HPV ; HSIL ; human papillomavirus ; human papillomavirus 16 ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; low grade squamous intraepithelial lesion ; LSIL ; Medical sciences ; open reading frame ; ORF ; Original ; Papillomaviridae - genetics ; Papillomavirus infections ; Papillomavirus Infections - virology ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; PCR ; polymerase chain reaction ; Polymerase Chain Reaction - methods ; Risk ; Risk factors ; saline sodium citrate ; SCC ; SDS ; sodium dodecyl sulfate ; Tumor Virus Infections - virology ; Tumors ; Uterine Cervical Dysplasia - virology ; Uterine Cervical Neoplasms - virology ; viral integration ; Virus Integration</subject><ispartof>Journal of clinical pathology, 2003-07, Vol.56 (7), p.532-536</ispartof><rights>Copyright 2003 Journal of Clinical Pathology</rights><rights>2003 INIST-CNRS</rights><rights>COPYRIGHT 2003 BMJ Publishing Group Ltd.</rights><rights>Copyright: 2003 Copyright 2003 Journal of Clinical Pathology</rights><rights>Copyright © Copyright 2003 Journal of Clinical Pathology 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b613t-d5466fef3c506256562ad961eefb8f85b3682ec38a5ee0443b5910fcc86dfcee3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1770000/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1770000/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=14912617$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12835300$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gallo, G</creatorcontrib><creatorcontrib>Bibbo, M</creatorcontrib><creatorcontrib>Bagella, L</creatorcontrib><creatorcontrib>Zamparelli, A</creatorcontrib><creatorcontrib>Sanseverino, F</creatorcontrib><creatorcontrib>Giovagnoli, M R</creatorcontrib><creatorcontrib>Vecchione, A</creatorcontrib><creatorcontrib>Giordano, A</creatorcontrib><title>Study of viral integration of HPV-16 in young patients with LSIL</title><title>Journal of clinical pathology</title><addtitle>J Clin Pathol</addtitle><description>Aims: To investigate the physical status of human papillomavirus 16 (HPV-16) in low grade squamous intraepithelial lesions (LSILs) as a means of determining the percentage of viral integration. Methods: Ninety two LSIL/HPV positive Thin Prep™ samples were initially tested for the E6 gene by the polymerase chain reaction (PCR) to identify the HPV-16 virus. To avoid false positive results, the specificity of the bands obtained from PCR was confirmed by Southern blot hybridisation with internal oligonucleotide probes. Next, a PCR screen for the E2 gene was performed to identify those samples in which the virus was integrated. Viral integration was detected in just over half of them. Results: Twenty of the 92 samples were HPV-16 positive, as shown by PCR for the E6 gene. Southern blot analysis confirmed that 13 of these samples were positive for the viral E6 gene. Thus, viral integration was detected in just over a half of the samples positive for HPV-16. Conclusions: These data show that HPV-16 integration occurs in a subset of LSILs. The measurement of HPV-16 integration would be a helpful complementary tool for cytological evaluation in primary cervical screening to identify those patients at risk of developing high grade squamous intraepithelial lesions and cervical cancer.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Squamous Cell - virology</subject><subject>Causes of</subject><subject>Cervical cancer</subject><subject>Complications and side effects</subject><subject>DNA, Viral - analysis</subject><subject>Female</subject><subject>Female genital diseases</subject><subject>Genetic aspects</subject><subject>Genital system. Mammary gland</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>high grade squamous intraepithelial lesion</subject><subject>HPV</subject><subject>HSIL</subject><subject>human papillomavirus</subject><subject>human papillomavirus 16</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>low grade squamous intraepithelial lesion</subject><subject>LSIL</subject><subject>Medical sciences</subject><subject>open reading frame</subject><subject>ORF</subject><subject>Original</subject><subject>Papillomaviridae - genetics</subject><subject>Papillomavirus infections</subject><subject>Papillomavirus Infections - virology</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. 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Mammary gland</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>high grade squamous intraepithelial lesion</topic><topic>HPV</topic><topic>HSIL</topic><topic>human papillomavirus</topic><topic>human papillomavirus 16</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>low grade squamous intraepithelial lesion</topic><topic>LSIL</topic><topic>Medical sciences</topic><topic>open reading frame</topic><topic>ORF</topic><topic>Original</topic><topic>Papillomaviridae - genetics</topic><topic>Papillomavirus infections</topic><topic>Papillomavirus Infections - virology</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>PCR</topic><topic>polymerase chain reaction</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Risk</topic><topic>Risk factors</topic><topic>saline sodium citrate</topic><topic>SCC</topic><topic>SDS</topic><topic>sodium dodecyl sulfate</topic><topic>Tumor Virus Infections - virology</topic><topic>Tumors</topic><topic>Uterine Cervical Dysplasia - virology</topic><topic>Uterine Cervical Neoplasms - virology</topic><topic>viral integration</topic><topic>Virus Integration</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gallo, G</creatorcontrib><creatorcontrib>Bibbo, M</creatorcontrib><creatorcontrib>Bagella, L</creatorcontrib><creatorcontrib>Zamparelli, A</creatorcontrib><creatorcontrib>Sanseverino, F</creatorcontrib><creatorcontrib>Giovagnoli, M R</creatorcontrib><creatorcontrib>Vecchione, A</creatorcontrib><creatorcontrib>Giordano, A</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gallo, G</au><au>Bibbo, M</au><au>Bagella, L</au><au>Zamparelli, A</au><au>Sanseverino, F</au><au>Giovagnoli, M R</au><au>Vecchione, A</au><au>Giordano, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Study of viral integration of HPV-16 in young patients with LSIL</atitle><jtitle>Journal of clinical pathology</jtitle><addtitle>J Clin Pathol</addtitle><date>2003-07-01</date><risdate>2003</risdate><volume>56</volume><issue>7</issue><spage>532</spage><epage>536</epage><pages>532-536</pages><issn>0021-9746</issn><eissn>1472-4146</eissn><coden>JCPAAK</coden><abstract>Aims: To investigate the physical status of human papillomavirus 16 (HPV-16) in low grade squamous intraepithelial lesions (LSILs) as a means of determining the percentage of viral integration. Methods: Ninety two LSIL/HPV positive Thin Prep™ samples were initially tested for the E6 gene by the polymerase chain reaction (PCR) to identify the HPV-16 virus. To avoid false positive results, the specificity of the bands obtained from PCR was confirmed by Southern blot hybridisation with internal oligonucleotide probes. Next, a PCR screen for the E2 gene was performed to identify those samples in which the virus was integrated. Viral integration was detected in just over half of them. Results: Twenty of the 92 samples were HPV-16 positive, as shown by PCR for the E6 gene. Southern blot analysis confirmed that 13 of these samples were positive for the viral E6 gene. Thus, viral integration was detected in just over a half of the samples positive for HPV-16. Conclusions: These data show that HPV-16 integration occurs in a subset of LSILs. The measurement of HPV-16 integration would be a helpful complementary tool for cytological evaluation in primary cervical screening to identify those patients at risk of developing high grade squamous intraepithelial lesions and cervical cancer.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and Association of Clinical Pathologists</pub><pmid>12835300</pmid><doi>10.1136/jcp.56.7.532</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Biological and medical sciences
Carcinoma, Squamous Cell - virology
Causes of
Cervical cancer
Complications and side effects
DNA, Viral - analysis
Female
Female genital diseases
Genetic aspects
Genital system. Mammary gland
Gynecology. Andrology. Obstetrics
high grade squamous intraepithelial lesion
HPV
HSIL
human papillomavirus
human papillomavirus 16
Humans
Investigative techniques, diagnostic techniques (general aspects)
low grade squamous intraepithelial lesion
LSIL
Medical sciences
open reading frame
ORF
Original
Papillomaviridae - genetics
Papillomavirus infections
Papillomavirus Infections - virology
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
PCR
polymerase chain reaction
Polymerase Chain Reaction - methods
Risk
Risk factors
saline sodium citrate
SCC
SDS
sodium dodecyl sulfate
Tumor Virus Infections - virology
Tumors
Uterine Cervical Dysplasia - virology
Uterine Cervical Neoplasms - virology
viral integration
Virus Integration
title Study of viral integration of HPV-16 in young patients with LSIL
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