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Sökning: onr:"swepub:oai:DiVA.org:oru-91909" > Optimization of dro...

Optimization of droplet digital PCR assays for the type specific detection and quantification of five HPV genotypes, also including additional data on viral load of nine different HPV genotypes in cervical carcinomas

Kaliff, Malin, 1985- (författare)
Örebro universitet,Institutionen för medicinska vetenskaper,Department of Laboratory Medicine
Louise, Bohr Mordhorst (författare)
Department of Oncology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden
Helenius, Gisela, 1973- (författare)
Örebro universitet,Institutionen för medicinska vetenskaper,Department of Laboratory Medicine
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Karlsson, Mats, 1960- (författare)
Örebro universitet,Institutionen för medicinska vetenskaper,Department of Laboratory Medicine
Lillsunde-Larsson, Gabriella, 1971- (författare)
Örebro universitet,Institutionen för medicinska vetenskaper,Department of Laboratory Medicine
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 (creator_code:org_t)
Elsevier, 2021
2021
Engelska.
Ingår i: Journal of Virological Methods. - : Elsevier. - 0166-0934 .- 1879-0984. ; 294
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The droplet digital PCR (ddPCR) system enables high-sensitivity detection of nucleic acids and direct absolute quantification of the targets. The aim of this research was to evaluate this system for viral load (VL) analysis of the human papillomavirus (HPV) genotypes HPV31, 35, 39, 51 and 56 measured in number of viral particles per cell. The sample types used for the optimization of the ddPCR assay were formalin-fixed paraffin-embedded (FFPE) tissues and cervical liquid cytology samples. The presently optimized ddPCR assays, together with assays optimized previously for HPV16, 18, 33 and 45, with the same ddPCR method, were used for the VL analysis of cervical tumor samples. Results published previously on the present study cohort showed that women with a cervical tumor containing multiple high-risk HPV genotypes had a worse prognosis compared to women with single-genotype-infected tumors. The VL was therefore analyzed in this study for the same cohort, as a possible explanatory factor to the prognostic differences. The results of the optimization part of the study, with analysis of VL using ddPCR in DNA from varying sample types (FFPE and liquid cytology samples), showed that each of the five assays demonstrated good inter- and intra-assay means with a coefficient of variation (CV) under 8% and 6% respectably. The cohort results showed no difference in VL between tumors with multiple and single HPV infections, and therefore did most likely not constitute a contributing factor for prognostic differences observed previously. However, tumors from women aged 60 years or older or containing certain HPV genotypes and genotype genera were associated with a higher VL.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Human papilloma virus
Papillomaviridae
cervical cancer
droplet digital PCR
uterine cervical neoplasms
viral load

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