HPV DNA genotyping, HPV E6*I mRNA detection, and p16


Journal

Cancer epidemiology
ISSN: 1877-783X
Titre abrégé: Cancer Epidemiol
Pays: Netherlands
ID NLM: 101508793

Informations de publication

Date de publication:
06 2021
Historique:
received: 24 09 2020
accepted: 26 02 2021
pubmed: 12 4 2021
medline: 8 7 2021
entrez: 11 4 2021
Statut: ppublish

Résumé

The main risk factors for head and neck cancer (HNC) are tobacco and alcohol use. However, an important fraction of oropharyngeal cancer (OPC) is caused by human papillomaviruses (HPV), a subgroup with increasing incidence in several western countries. As part of the HPV-AHEAD study, we assessed the role of HPV infection in 772 archived tissue specimens of Belgian HNC patients: 455 laryngeal (LC), 106 oral cavity (OCC), 99 OPC, 76 hypopharyngeal (HC), and 36 unspecified parts of the head and neck. All specimens were tested for HPV DNA (21 genotypes); whereof all HPV DNA-positives, all HPV DNA-negative OPCs and a random subset of HPV DNA-negatives of the other HNC-sites were tested for the presence of type-specific HPV RNA and p16 The highest HPV DNA prevalence was observed in OPC (36.4 %), and was significantly lower (p < 0.001) in the other HNCs (OCC:7.5 %, LC:6.6 %). HPV16 was the most common HPV-genotype in all HNCs. Approximately 83.0 % of the HPV DNA-positive OPCs tested HPV RNA or p16-positive, compared to about 37.5 % and 44.0 % in OCC and LC, respectively. Estimation of the attributable fraction of an HPV infection in HNC was very similar for HPV RNA or p16 in addition to DNA-positivity; with 30 % for OPC, and 3 % for OCC and LC. Our study confirms the heterogeneity of HPV DNA prevalence across anatomical sites in HNC, with a predominance of HPV16 in all sites. The estimated proportion of HPV-driven HNC in Belgium, during the period 1980-2014, was 10 times higher in OPC compared to OCC and LC.

Sections du résumé

BACKGROUND
The main risk factors for head and neck cancer (HNC) are tobacco and alcohol use. However, an important fraction of oropharyngeal cancer (OPC) is caused by human papillomaviruses (HPV), a subgroup with increasing incidence in several western countries.
METHODS
As part of the HPV-AHEAD study, we assessed the role of HPV infection in 772 archived tissue specimens of Belgian HNC patients: 455 laryngeal (LC), 106 oral cavity (OCC), 99 OPC, 76 hypopharyngeal (HC), and 36 unspecified parts of the head and neck. All specimens were tested for HPV DNA (21 genotypes); whereof all HPV DNA-positives, all HPV DNA-negative OPCs and a random subset of HPV DNA-negatives of the other HNC-sites were tested for the presence of type-specific HPV RNA and p16
RESULTS
The highest HPV DNA prevalence was observed in OPC (36.4 %), and was significantly lower (p < 0.001) in the other HNCs (OCC:7.5 %, LC:6.6 %). HPV16 was the most common HPV-genotype in all HNCs. Approximately 83.0 % of the HPV DNA-positive OPCs tested HPV RNA or p16-positive, compared to about 37.5 % and 44.0 % in OCC and LC, respectively. Estimation of the attributable fraction of an HPV infection in HNC was very similar for HPV RNA or p16 in addition to DNA-positivity; with 30 % for OPC, and 3 % for OCC and LC.
CONCLUSION
Our study confirms the heterogeneity of HPV DNA prevalence across anatomical sites in HNC, with a predominance of HPV16 in all sites. The estimated proportion of HPV-driven HNC in Belgium, during the period 1980-2014, was 10 times higher in OPC compared to OCC and LC.

Identifiants

pubmed: 33839457
pii: S1877-7821(21)00042-4
doi: 10.1016/j.canep.2021.101925
pii:
doi:

Substances chimiques

Cyclin-Dependent Kinase Inhibitor p16 0
DNA, Viral 0
E6 protein, human papillomavirus type 1 0
Ki-67 Antigen 0
Oncogene Proteins, Viral 0
RNA, Messenger 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

101925

Investigateurs

Christel Herold-Mende (C)
Gerhard Dyckhoff (G)
George Mosialos (G)
Fausto Chiesa (F)
Marta Tagliabue (M)
Mohssen Ansarin (M)
Heiner Boeing (H)
Xavier Castellsagué (X)
Silvia de Sanjosé (S)
Marisa Mena (M)
Francesc Xavier Bosch (FX)
Laia Alemany (L)
Pulikottil Okkuru Esmy (PO)
Rudrapatna S Jayshree (RS)
Kortikere S Sabitha (KS)
Ashok M Shenoy (AM)
Manavalan Vijayakumar (M)
Aruna S Chiwate (AS)
Ranjit V Thorat (RV)
Girish G Hublikar (GG)
Shashikant S Lakshetti (SS)
Bhagwan M Nene (BM)
Amal Ch Kataki (AC)
Ashok Kumar Das (A)
Subha Sankaran (S)
Kunnambath Ramadas (K)
Christine Carreira (C)
Sandrine McKay-Chopin (S)
Thara Somanathan (T)
Alfredo Zito (A)

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Auteurs

Cindy Simoens (C)

Unit of Cancer Epidemiology, Cancer Centre, Sciensano, Brussels, Belgium; AMBIOR, Laboratory for Cell Biology & Histology, University of Antwerp, Antwerp, Belgium. Electronic address: cindy.simoens@sciensano.be.

Ivana Gorbaslieva (I)

AMBIOR, Laboratory for Cell Biology & Histology, University of Antwerp, Antwerp, Belgium.

Tarik Gheit (T)

Infections and Cancer Biology Group, International Agency for Research on Cancer (IARC), Lyon, France.

Dana Holzinger (D)

Infections and Cancer Epidemiology, Research Program Infection, Inflammation and Cancer, Deutsches Krebsforschungszentrum, Heidelberg, Germany.

Eric Lucas (E)

Infections and Cancer Biology Group, International Agency for Research on Cancer (IARC), Lyon, France.

Ruediger Ridder (R)

Roche Mtm Laboratories, Mannheim, Germany; Ventana Medical Systems, Inc. (Roche Tissue Diagnostics), Tucson, AZ, USA.

Susanne Rehm (S)

Roche Mtm Laboratories, Mannheim, Germany.

Peter Vermeulen (P)

Laboratory for Pathological Anatomy, Sint Augustinus Hospital, GZA, Antwerp, Belgium.

Martin Lammens (M)

Department of Pathology, Antwerp University Hospital, Edegem, Belgium; Center for Oncological Research, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.

Olivier M Vanderveken (OM)

Department of Otorhinolaryngology, Head and Neck Surgery, Antwerp University Hospital, Edegem, Belgium; Department of Translational Neurosciences, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.

Rekha Vijay Kumar (RV)

Kidwai Memorial Institute of Oncology, Bangalore, Karnataka, 560029, India.

Nitin Gangane (N)

Mahatma Gandhi Institute of Medical Sciences, Sevagram, Wardha, Maharashtra State, 442102, India.

Alessandro Caniglia (A)

IRCCS Istituto Tumori "Giovanni Paolo II", Bari, Italy.

Fausto Maffini (F)

Division of Pathology, Instituto Europeo di Oncologia (IEO), Milan, Italy.

Maria Belén Lloveras Rubio (MBL)

Hospital del Mar, Parc de Salut Mar, Pg/Marítim 25-29, Barcelona, 08003, Spain.

Devasena Anantharaman (D)

Rajiv Gandhi Centre for Biotechnology, Poojappura, Thiruvananthapuram, Kerala, 695014, India.

Susanna Chiocca (S)

Department of Experimental Oncology, IEO, European Institute of Oncology IRCCS, Milan, Italy.

Paul Brennan (P)

Section of Genetics, International Agency for Research on Cancer (IARC), Lyon, France.

Madhavan Radhakrishna Pillai (MR)

Rajiv Gandhi Centre for Biotechnology, Poojappura, Thiruvananthapuram, Kerala, 695014, India.

Rengaswamy Sankaranarayanan (R)

Research Triangle Institute (RTI) International India, New Delhi, India.

Johannes Bogers (J)

AMBIOR, Laboratory for Cell Biology & Histology, University of Antwerp, Antwerp, Belgium.

Michael Pawlita (M)

Infections and Cancer Epidemiology, Research Program Infection, Inflammation and Cancer, Deutsches Krebsforschungszentrum, Heidelberg, Germany.

Massimo Tommasino (M)

Infections and Cancer Biology Group, International Agency for Research on Cancer (IARC), Lyon, France.

Marc Arbyn (M)

Unit of Cancer Epidemiology, Cancer Centre, Sciensano, Brussels, Belgium. Electronic address: marc.arbyn@sciensano.be.

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Classifications MeSH