Absence of an association of human polyomavirus and papillomavirus infection with lung cancer in China: a nested case–control study
Creators
- 1. Institute for Health Metrics and Evaluation, University of Washington, 2301 5th Avenue, Suite 600, Seattle, WA 98121 (United States)
- 2. Fred Hutchinson Cancer Research Center, Seattle, WA (United States)
- 3. Department of Epidemiology, School of Public Health, University of Washington, Seattle, WA (United States)
- 4. Department of Biostatistics, School of Public Health, University of Washington, Seattle, WA (United States)
- 5. Department of Cancer Epidemiology, Cancer Institute, Chinese Academy of Medical Sciences, Beijing (China)
- 6. Genetic Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda (United States)
- 7. Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC (United States)
Description
Studies of human polyomavirus (HPyV) infection and lung cancer are limited and those regarding the association of human papillomavirus (HPV) infection and lung cancer have produced inconsistent results. We conducted a nested case–control study to assess the association between incident lung cancer of various histologies and evidence of prior infection with HPyVs and HPVs. We selected serum from 183 cases and 217 frequency matched controls from the Yunnan Tin Miner's Cohort study, which was designed to identify biomarkers for early detection of lung cancer. Using multiplex liquid bead microarray (LBMA) antibody assays, we tested for antibodies to the VP1 structural protein and small T antigen (ST-Ag) of Merkel cell, KI, and WU HPyVs. We also tested for antibodies against HPV L1 structural proteins (high-risk types 16, 18, 31, 33, 52, and 58 and low-risk types 6 and 11) and E6 and E7 oncoproteins (high risk types 16 and 18). Measures of antibody reactivity were log transformed and analyzed using logistic regression. We found no association between KIV, WUV, and MCV antibody levels and incident lung cancer (P-corrected for multiple comparisons >0.10 for all trend tests). We also found no association with HPV-16, 18, 31, 33, 52, and 58 seropositivity (P-corrected for multiple comparisons >0.05 for all). Future studies of infectious etiologies of lung cancer should look beyond HPyVs and HPVs as candidate infectious agents. The online version of this article (doi:10.1186/s12885-016-2381-3) contains supplementary material, which is available to authorized users
Availability note (English)
Available from http://dx.doi.org/10.1186/s12885-016-2381-3; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4888628Additional details
Identifiers
Publishing Information
- Journal Title
- BMC cancer (Online)
- Journal Volume
- 16
- Journal Page Range
- vp.
- ISSN
- 1471-2407
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47088091
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- ANTIBODIES; BIOLOGICAL MARKERS; LUNGS; NEOPLASMS
- Descriptors DEC
- BODY; DISEASES; ORGANS; RESPIRATORY SYSTEM
Optional Information
- Copyright
- Copyright (c) The Author(s). 2016
- Notes
- PMCID: PMC4888628; PMID: 27246610; PUBLISHER-ID: 2381; OAI: oai:pubmedcentral.nih.gov:4888628