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

被引:52
作者
Gallo, G
Bibbo, M
Bagella, L
Zamparelli, A
Sanseverino, F
Giovagnoli, MR
Vecchione, A
Giordano, A
机构
[1] Temple Univ, Coll Sci & Technol, Sbarro Inst Canc Res & Mol Med, Philadelphia, PA 19122 USA
[2] Univ Roma La Sapienza, Sch Med 2, I-00100 Rome, Italy
[3] Thomas Jefferson Univ, Jefferson Med Coll, Dept Pathol Anat & Cell Biol, Philadelphia, PA 19107 USA
[4] Univ Siena, Dept Obstet & Gynecol, I-53100 Siena, Italy
[5] Univ Roma La Sapienza, Sch Med 2, I-00161 Rome, Italy
[6] Univ Roma La Sapienza, Sch Specializat Oncol, I-00161 Rome, Italy
关键词
D O I
10.1136/jcp.56.7.532
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
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(R) 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.
引用
收藏
页码:532 / 536
页数:5
相关论文
共 59 条
[1]   HUMAN PAPILLOMAVIRUS TYPE-18 ASSOCIATES WITH MORE ADVANCED CERVICAL NEOPLASIA THAN HUMAN PAPILLOMAVIRUS TYPE-16 [J].
ARENDS, MJ ;
DONALDSON, YK ;
DUVALL, E ;
WYLLIE, AH ;
BIRD, CC .
HUMAN PATHOLOGY, 1993, 24 (04) :432-437
[2]   PAPILLOMAVIRUSES AND HUMAN CANCER [J].
ARENDS, MJ ;
WYLLIE, AH ;
BIRD, CC .
HUMAN PATHOLOGY, 1990, 21 (07) :686-698
[3]   HPV IN FULL THICKNESS CERVICAL BIOPSIES - HIGH PREVALENCE IN CIN-2 AND CIN-3 DETECTED BY A SENSITIVE PCR METHOD [J].
ARENDS, MJ ;
DONALDSON, YK ;
DUVALL, E ;
WYLLIE, AH ;
BIRD, CC .
JOURNAL OF PATHOLOGY, 1991, 165 (04) :301-309
[4]   HPV16 and HPV18 in genital tumors: Significantly different levels of viral integration and correlation to tumor invasiveness [J].
Badaracco, G ;
Venuti, A ;
Sedati, A ;
Marcante, ML .
JOURNAL OF MEDICAL VIROLOGY, 2002, 67 (04) :574-582
[5]   STRUCTURAL AND TRANSCRIPTIONAL ANALYSIS OF HUMAN PAPILLOMAVIRUS TYPE-16 SEQUENCES IN CERVICAL-CARCINOMA CELL-LINES [J].
BAKER, CC ;
PHELPS, WC ;
LINDGREN, V ;
BRAUN, MJ ;
GONDA, MA ;
HOWLEY, PM .
JOURNAL OF VIROLOGY, 1987, 61 (04) :962-971
[6]   Genomic cloning and characterization of the nonoccupied allele corresponding to the integration site of human papillomavirus type 16 DNA in the cervical cancer cell line SiHa [J].
BauerHofmann, R ;
Borghouts, C ;
Auvinen, E ;
Bourda, E ;
Rosl, F ;
Alonso, A .
VIROLOGY, 1996, 217 (01) :33-41
[7]   A PROSPECTIVE-STUDY OF COLPOSCOPY IN WOMEN WITH MILD DYSKARYOSIS OR KOILOCYTOSIS [J].
BOLGER, BS ;
LEWIS, BV .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1988, 95 (11) :1117-1119
[8]   Use of the polymerase chain reaction to specifically amplify integrated HPV-16 DNA by virtue of its linkage to interspersed repetitive DNA [J].
Carmody, MW ;
Jones, M ;
Tarraza, H ;
Vary, CPH .
MOLECULAR AND CELLULAR PROBES, 1996, 10 (02) :107-116
[9]  
Choo KB, 1996, J MED VIROL, V49, P15, DOI 10.1002/(SICI)1096-9071(199605)49:1<15::AID-JMV3>3.3.CO
[10]  
2-4