Human papillomaviruses in skin cancer and cervical cancer
Author
Summary, in English
The causal relationship between persistent genital infections with human
papillomavirus (HPV) and development of cervical cancer is well established.
In contrast, the significance of infections with cutaneous HPV for development
of non-melanoma skin cancer (NMSC) is not well understood. We have evaluated
whether seropositivity to cutaneous HPV is a marker for cutaneous HPV
infection and used high throughput HPV serology to investigate the risk for
developing NMSC in relation to seropositivity for cutaneous HPV infection and
PCR techniques to investigate the risk for NMSC in relation to presence of HPV
DNA in the skin. We have also investigated how different sexually transmitted
infections interact with HPV in the aetiology of cervical cancer.
Two of our NMSC studies were hospital-based case-control studies where
biopsies from skin tumours and healthy skin were analysed for presence of HPV
DNA and serum samples for presence of antibodies to 14 different HPV types.
The third NMSC study and the cervical cancer study were designed as prospective
biobank-based case-control studies where biobanks were linked to cancer
registries for identification of cancers that have occurred after donation of a
serum sample. For patients with cervix cancer also formalin-fixed paraffin embedded
tumour tissue was retrieved and tested for HPV DNA.
In the skin cancer studies, we found that both DNA and seropositivity to
HPV of genus beta species 2 associated with an increased risk for development of
squamous cell carcinoma (SCC) of the skin and that sun-exposure is a risk factor
for cutaneous HPV infection. In the cervical cancer study we found in addition
to the exposure to the oncogenic HPV type that is found in the cancer tissue,
that history of Chlamydia trachomatis stood out among the different sexually
transmitted infections as being associated with increased risk for cervical cancer,
suggesting that it may acts as a co-factor to HPV in cervical carcinogenesis.
papillomavirus (HPV) and development of cervical cancer is well established.
In contrast, the significance of infections with cutaneous HPV for development
of non-melanoma skin cancer (NMSC) is not well understood. We have evaluated
whether seropositivity to cutaneous HPV is a marker for cutaneous HPV
infection and used high throughput HPV serology to investigate the risk for
developing NMSC in relation to seropositivity for cutaneous HPV infection and
PCR techniques to investigate the risk for NMSC in relation to presence of HPV
DNA in the skin. We have also investigated how different sexually transmitted
infections interact with HPV in the aetiology of cervical cancer.
Two of our NMSC studies were hospital-based case-control studies where
biopsies from skin tumours and healthy skin were analysed for presence of HPV
DNA and serum samples for presence of antibodies to 14 different HPV types.
The third NMSC study and the cervical cancer study were designed as prospective
biobank-based case-control studies where biobanks were linked to cancer
registries for identification of cancers that have occurred after donation of a
serum sample. For patients with cervix cancer also formalin-fixed paraffin embedded
tumour tissue was retrieved and tested for HPV DNA.
In the skin cancer studies, we found that both DNA and seropositivity to
HPV of genus beta species 2 associated with an increased risk for development of
squamous cell carcinoma (SCC) of the skin and that sun-exposure is a risk factor
for cutaneous HPV infection. In the cervical cancer study we found in addition
to the exposure to the oncogenic HPV type that is found in the cancer tissue,
that history of Chlamydia trachomatis stood out among the different sexually
transmitted infections as being associated with increased risk for cervical cancer,
suggesting that it may acts as a co-factor to HPV in cervical carcinogenesis.
Department/s
- EpiHealth: Epidemiology for Health
- BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation
- Epidemiology
- Clinical Microbiology, Malmö
Publishing year
2010
Language
English
Publication/Series
Lund University Faculty of Medicine Doctoral Dissertation Series
Volume
2010:40
Full text
Document type
Dissertation
Publisher
Department of Medical Microbiology, Lund University
Topic
- Microbiology in the medical area
Keywords
- Human papillomavirus
- serology co-factors
- non-melanoma skin cancer
Status
Published
Research group
- Institution of Laboratory Medicine, Medical Microbiolgy, Respiratory Pathogen Group
- Epidemiology
- Clinical Microbiology, Malmö
Supervisor
- Joakim Dillner
- Ola Forslund
- Lisen Arnheim
ISBN/ISSN/Other
- ISSN: 1652-8220
- ISBN: 978-91-86443-55-9
Defence date
22 April 2010
Defence time
09:00
Defence place
lecturing hall pathology department, Malmö
Opponent
- michel favre (professor)