Infections in skin cancer
Author: Arroyo Mühr, Laila Sara
Date: 2016-04-08
Location: Solen 4U, Alfred Nobels Allé 8, plan 4, Karolinska Institutet, Huddinge
Time: 13.00
Department: Inst för laboratoriemedicin / Dept of Laboratory Medicine
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Thesis (2.292Mb)
Abstract
The increasing prevalence of skin cancer results in that it will soon equal that of all other
cancers combined. Sun exposure is a well-known risk factor for its development, but
despite the growing public awareness of the harmful consequences of ultraviolet
radiation, the cancer incidence continues to increase, implying that other factors might
also have a role in promoting this disease.
Data from immunosuppressed patients reveals a 100-fold increased incidence of nonmelanoma skin carcinoma (NMSC), but an infectious etiology has not been established. However, certain human papillomaviruses (HPVs) have previously been detected in this type of cancer.
We applied high throughput sequencing to different skin lesions in order to assess which organisms were present. Most viral reads (>95%) belonged to human papillomavirus.
Traditionally, viral detection was performed using PCR methods. We used degenerate “general” HPV primers and multiplexed novel “specific” HPV primers in order to amplify a broad number of HPVs by PCR. This method showed a very high sensitivity, but the HPV types with low similarity to the primer sequences might have escaped amplification. Therefore, we performed an unbiased approach based on non-PCR whole genome amplification, independent of sequence information, in order to detect those “escaping” HPV types, as well as to determine if other viruses were present in the samples.
Overall, we identified almost 100 putative novel HPV types in total, and characterized 4 novel HPV types (HPV 197, 200, 201 and 202). Most of the HPV types were detected in very few patients each, and at a very low viral load (below 0.5 copies/cell), except for HPV 197, which was the most commonly found virus in skin tumors (37.4% of skin lesions). Despite the higher sensitivity of PCR methods, the unbiased approach detected HPV in 37/40 condyloma acuminata that had been reported as “HPV-negative” with specific PCR techniques. Certain HPV types, including HPV 197, were not detected by PCR and only by non-PCR based methods. Therefore, more unbiased PCR-independent methods are needed to describe which organisms are most commonly present in skin lesions.
The work in this thesis has expanded our knowledge of the wide genomic diversity of HPV on the skin, and finds that PCR-independent methods are needed to describe which organisms are most commonly present in skin lesions. Further studies are needed to assess any possible role of viral infections in skin cancer, elucidation of mechanistic effects and determine the direction of causality of any associations.
Data from immunosuppressed patients reveals a 100-fold increased incidence of nonmelanoma skin carcinoma (NMSC), but an infectious etiology has not been established. However, certain human papillomaviruses (HPVs) have previously been detected in this type of cancer.
We applied high throughput sequencing to different skin lesions in order to assess which organisms were present. Most viral reads (>95%) belonged to human papillomavirus.
Traditionally, viral detection was performed using PCR methods. We used degenerate “general” HPV primers and multiplexed novel “specific” HPV primers in order to amplify a broad number of HPVs by PCR. This method showed a very high sensitivity, but the HPV types with low similarity to the primer sequences might have escaped amplification. Therefore, we performed an unbiased approach based on non-PCR whole genome amplification, independent of sequence information, in order to detect those “escaping” HPV types, as well as to determine if other viruses were present in the samples.
Overall, we identified almost 100 putative novel HPV types in total, and characterized 4 novel HPV types (HPV 197, 200, 201 and 202). Most of the HPV types were detected in very few patients each, and at a very low viral load (below 0.5 copies/cell), except for HPV 197, which was the most commonly found virus in skin tumors (37.4% of skin lesions). Despite the higher sensitivity of PCR methods, the unbiased approach detected HPV in 37/40 condyloma acuminata that had been reported as “HPV-negative” with specific PCR techniques. Certain HPV types, including HPV 197, were not detected by PCR and only by non-PCR based methods. Therefore, more unbiased PCR-independent methods are needed to describe which organisms are most commonly present in skin lesions.
The work in this thesis has expanded our knowledge of the wide genomic diversity of HPV on the skin, and finds that PCR-independent methods are needed to describe which organisms are most commonly present in skin lesions. Further studies are needed to assess any possible role of viral infections in skin cancer, elucidation of mechanistic effects and determine the direction of causality of any associations.
List of papers:
I. Arroyo Mühr LS, Smelov V, Bzhalava D, Eklund C, Hultin E, Dillner J. Next generation sequencing for human papillomavirus genotyping. J Clin Virology 2013;58:437-42.
Fulltext (DOI)
Pubmed
View record in Web of Science®
II. Ekström J, Arroyo Mühr LS, Bzhalava D, Söderlund-Strand A, Hultin E, Nordin P, Stenquist B, Paoli J, Forslund O, Dillner J. Diversity of human papillomaviruses in skin lesions. Virology 2013;447:300-11.
Fulltext (DOI)
Pubmed
View record in Web of Science®
III. Bzhalava D, Arroyo Mühr LS, Lagheden C, Ekström J, Forslund O, Dillner J, Hultin E. Deep sequencing extends the diversity of human papillomaviruses in human skin. Scientific Reports 2014;4:5807.
Fulltext (DOI)
Pubmed
View record in Web of Science®
IV. Arroyo Mühr LS, Hultin E, Bzhalava D, Eklund C, Lagheden C, Ekström J, Johansson H, Forslund O, Dillner J. Human papillomavirus type 197 is commonly present in skin tumors. Int J Cancer 2015;136:2546-55.
Fulltext (DOI)
Pubmed
View record in Web of Science®
V. Arroyo Mühr LS, Bzhalava D, Lagheden C, Eklund C, Johansson H, Forslund O, Dillner J, Hultin E. Does human papillomavirus-negative condylomata exist? Virology 2015;485:283-8.
Fulltext (DOI)
Pubmed
View record in Web of Science®
I. Arroyo Mühr LS, Smelov V, Bzhalava D, Eklund C, Hultin E, Dillner J. Next generation sequencing for human papillomavirus genotyping. J Clin Virology 2013;58:437-42.
Fulltext (DOI)
Pubmed
View record in Web of Science®
II. Ekström J, Arroyo Mühr LS, Bzhalava D, Söderlund-Strand A, Hultin E, Nordin P, Stenquist B, Paoli J, Forslund O, Dillner J. Diversity of human papillomaviruses in skin lesions. Virology 2013;447:300-11.
Fulltext (DOI)
Pubmed
View record in Web of Science®
III. Bzhalava D, Arroyo Mühr LS, Lagheden C, Ekström J, Forslund O, Dillner J, Hultin E. Deep sequencing extends the diversity of human papillomaviruses in human skin. Scientific Reports 2014;4:5807.
Fulltext (DOI)
Pubmed
View record in Web of Science®
IV. Arroyo Mühr LS, Hultin E, Bzhalava D, Eklund C, Lagheden C, Ekström J, Johansson H, Forslund O, Dillner J. Human papillomavirus type 197 is commonly present in skin tumors. Int J Cancer 2015;136:2546-55.
Fulltext (DOI)
Pubmed
View record in Web of Science®
V. Arroyo Mühr LS, Bzhalava D, Lagheden C, Eklund C, Johansson H, Forslund O, Dillner J, Hultin E. Does human papillomavirus-negative condylomata exist? Virology 2015;485:283-8.
Fulltext (DOI)
Pubmed
View record in Web of Science®
Institution: Karolinska Institutet
Supervisor: Dillner, Joakim
Issue date: 2016-03-07
Rights:
Publication year: 2016
ISBN: 978-91-7676-215-8
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