Background: Lung cancer in never smokers is a significant contributor of cancer mortality worldwide. In this analysis, we explored the role of nine human polyomaviruses, including JC virus (JCV), BK virus (BKV) and Merkel cell virus (MCV), in lung cancer development in never smokers as there are data to support that polyomaviruses are potentially carcinogenic in the human lung. Methods: We used multiplex serology to detect serum antibodies to polyomaviruses in a nested case-control design combining lung cancer cases and controls from four cohort studies - NYU Women's Health Study (NYU-WHS), Janus Serum Bank, Shanghai Women's Health Study and Singapore Chinese Health Study (SCHS). Results: The final analyses included 511 cases and 508 controls. Seroprevalence for each polyomavirus showed significant heterogeneity by study, but overall there were no statistically significant differences between cases and controls. In total, 69.1% of the cases and 68.7% of the controls were seropositive for JCV VP1 antibody. Seropositivity for BKV was higher at 89.0% in cases and 89.8% in controls and lower for MCV at 59.3% in cases and 61.6% in controls. Similar results were obtained after adding an additional retrospective case-control study (Xuanwei study) to the analysis. Conclusions: Our results do not support the hypothesis that seropositivity for polyomaviruses is associated with increased lung cancer risk in never smokers. Future research to evaluate relationship between polyomavirus infection and lung carcinogenesis should focus more on evaluating the presence of virus or viral nucleic acids (DNA or RNA) in lung tumour samples. © 2016 Cancer Research UK. All rights reserved.

Serum biomarkers of polyomavirus infection and risk of lung cancer in never smokers / Malhotra, J.; Waterboer, T.; Pawlita, M.; Michel, A.; Cai, Q.; Zheng, W.; Gao, Y.-T.; Lan, Q.; Rothman, N.; Langseth, H.; Grimsrud, T.K.; Yuan, J.-M.; Koh, W.-P.; Wang, R.; Arslan, A.A.; Zeleniuch-Jacquotte, A.; Boffetta, P.. - In: BRITISH JOURNAL OF CANCER. - ISSN 0007-0920. - ELETTRONICO. - 115:9(2016), pp. 1131-1139. [10.1038/bjc.2016.285]

Serum biomarkers of polyomavirus infection and risk of lung cancer in never smokers

Boffetta, P.
2016

Abstract

Background: Lung cancer in never smokers is a significant contributor of cancer mortality worldwide. In this analysis, we explored the role of nine human polyomaviruses, including JC virus (JCV), BK virus (BKV) and Merkel cell virus (MCV), in lung cancer development in never smokers as there are data to support that polyomaviruses are potentially carcinogenic in the human lung. Methods: We used multiplex serology to detect serum antibodies to polyomaviruses in a nested case-control design combining lung cancer cases and controls from four cohort studies - NYU Women's Health Study (NYU-WHS), Janus Serum Bank, Shanghai Women's Health Study and Singapore Chinese Health Study (SCHS). Results: The final analyses included 511 cases and 508 controls. Seroprevalence for each polyomavirus showed significant heterogeneity by study, but overall there were no statistically significant differences between cases and controls. In total, 69.1% of the cases and 68.7% of the controls were seropositive for JCV VP1 antibody. Seropositivity for BKV was higher at 89.0% in cases and 89.8% in controls and lower for MCV at 59.3% in cases and 61.6% in controls. Similar results were obtained after adding an additional retrospective case-control study (Xuanwei study) to the analysis. Conclusions: Our results do not support the hypothesis that seropositivity for polyomaviruses is associated with increased lung cancer risk in never smokers. Future research to evaluate relationship between polyomavirus infection and lung carcinogenesis should focus more on evaluating the presence of virus or viral nucleic acids (DNA or RNA) in lung tumour samples. © 2016 Cancer Research UK. All rights reserved.
2016
Serum biomarkers of polyomavirus infection and risk of lung cancer in never smokers / Malhotra, J.; Waterboer, T.; Pawlita, M.; Michel, A.; Cai, Q.; Zheng, W.; Gao, Y.-T.; Lan, Q.; Rothman, N.; Langseth, H.; Grimsrud, T.K.; Yuan, J.-M.; Koh, W.-P.; Wang, R.; Arslan, A.A.; Zeleniuch-Jacquotte, A.; Boffetta, P.. - In: BRITISH JOURNAL OF CANCER. - ISSN 0007-0920. - ELETTRONICO. - 115:9(2016), pp. 1131-1139. [10.1038/bjc.2016.285]
Malhotra, J.; Waterboer, T.; Pawlita, M.; Michel, A.; Cai, Q.; Zheng, W.; Gao, Y.-T.; Lan, Q.; Rothman, N.; Langseth, H.; Grimsrud, T.K.; Yuan, J.-M.; Koh, W.-P.; Wang, R.; Arslan, A.A.; Zeleniuch-Jacquotte, A.; Boffetta, P.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/671767
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