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Type-Specific Viral Load and Physical State of HPV Type 16, 18, and 58 as Diagnostic Biomarkers for High-Grade Squamous Intraepithelial Lesions or Cervical Cancer.
Kim, Jongseung; Kim, Bu Kyung; Jeon, Dongsoo; Lee, Chae Hyeong; Roh, Ju-Won; Kim, Joo-Young; Park, Sang-Yoon.
Afiliação
  • Kim J; Department of Family Medicine, Seoul Metropolitan Government Seoul National University Boramae Medical Center, Seoul, Korea.
  • Kim BK; Department of Tumor Biology, Seoul National University, Seoul, Korea.
  • Jeon D; Department of Obstetrics and Gynecology, Soonchunhyang University College of Medicine, Gumi, Korea.
  • Lee CH; Department of Obstetrics and Gynecology, Dongguk University Ilsan Hospital, Goyang, Korea.
  • Roh JW; Department of Obstetrics and Gynecology, Dongguk University Ilsan Hospital, Goyang, Korea.
  • Kim JY; Proton Therapy Center, Research Institute and Hospital, National Cancer Center, Goyang, Korea.
  • Park SY; Center for Uterine Cancer, Research Institute and Hospital, National Cancer Center, Goyang, Korea.
Cancer Res Treat ; 52(2): 396-405, 2020 Apr.
Article em En | MEDLINE | ID: mdl-31476849
ABSTRACT

PURPOSE:

High rate of false-positive tests is a major obstacle to use human papillomavirus (HPV) detection as a diagnostic tool for high-grade squamous intraepithelial lesions or cervical cancer (HSIL+). We investigated whether type-specific viral load or physical state of HPV 16, 18, and 58 are useful biomarkers for HSIL+. MATERIALS AND

METHODS:

Type-specific viral loads of E6 and E2 genes in cervical cells from 240, 83, and 79 HPV 16-, 18-, and 58-infected women, respectively, were determined using real-time polymerase chain reaction. Viral loads were normalized to cellular DNA (copy/cell). Total and integrated viral loads and physical state were compared between HSIL+ and controls, and diagnostic value was determined using receiver operating characteristic analysis.

RESULTS:

Viral loads of HPV 16, 18, and 58 were significantly different in lesions in the same pathologic grade. High type-specific total viral loads were significantly associated with HSIL+ (odds ratio [OR], 14.065, 39.472, and 7.103 for HPV 16, 18, and 58, respectively). High integrated viral load was related to HSIL+ in women with HPV 16 (OR, 8.242), and integrated state was associated with HSIL+ in women with HPV 18 (OR, 9.443). Type-specific total viral load was significantly associated with HSIL+ (area under curve, 0.914, 0.937, and 0.971 for HPV 16, 18, and 58, respectively), indicating an excellent performance in detecting HSIL+.

CONCLUSION:

Type-specific total viral load may be a powerful diagnostic marker for HSIL+ in HPV 16-, 18-, and 58-infected HSIL+ lesions. If demonstrated in all other high-risk HPV types, this method can lead to a paradigm shift in the strategy of equivocal cytologic abnormalities.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Papillomaviridae / Neoplasias do Colo do Útero / Carga Viral / Lesões Intraepiteliais Escamosas Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Papillomaviridae / Neoplasias do Colo do Útero / Carga Viral / Lesões Intraepiteliais Escamosas Idioma: En Ano de publicação: 2020 Tipo de documento: Article