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Simian virus 40 in human cancers - 28/08/11

Doi : 10.1016/S0002-9343(03)00087-1 
Regis A Vilchez, MD a, c, , Claudia A Kozinetz, PhD, MPH b, Amy S Arrington c, Charles R Madden, PhD c, Janet S Butel, PhD c
a Department of Medicine (RAV), Baylor College of Medicine, Houston, Texas, USA 
b Department of Pediatrics (CAK), Baylor College of Medicine, Houston, Texas, USA 
c Department of Molecular Virology and Microbiology (RAV, ASA, CRM, JSB), Baylor College of Medicine, Houston, Texas, USA 

*Requests for reprints should be addressed to Regis A. Vilchez, MD, Department of Medicine, Section of Infectious Diseases, Baylor College of Medicine, BCM 286, Room N1319, One Baylor Plaza, Houston, Texas 77030, USA

Abstract

Background

Many studies have reported the presence of simian virus 40 (SV40) deoxyribonucleic acid (DNA) or protein in human brain tumors and bone cancers, malignant mesothelioma, and non-Hodgkin’s lymphoma. However, the small samples and lack of control groups in some reports have made it difficult to assess their reliability.

Methods

Studies were included in this analysis if they met the following criteria: original studies of patients with primary brain tumors and bone cancers, malignant mesothelioma, or non-Hodgkin’s lymphoma; the investigation of SV40 was performed on primary cancer specimens; the analysis included a control group; and the same technique was used for cases and controls. Included reports were published from 1975 to 2002.

Results

Thirteen studies fulfilled the criteria for the investigation of primary brain cancers (661 tumors and 482 control samples). Specimens from patients with brain tumors were almost four times more likely to have evidence of SV40 infection than were those from controls (odds ratio [OR] = 3.9; 95% confidence interval [CI]: 2.6 to 5.8). The association was even stronger for mesothelioma (OR = 17; 95% CI: 10 to 28; based on 15 studies with 528 mesothelioma samples and 468 control samples) and for bone cancer (OR = 25; 95% CI: 6.8 to 88; based on four studies with 303 cancers and 121 control samples). SV40 DNA was also more frequent in samples from patients with non-Hodgkin’s lymphoma (OR = 5.4; 95% CI: 3.1 to 9.3; based on three studies with 301 cases and 578 control samples) than from controls.

Conclusion

These results establish that SV40 is associated significantly with brain tumors, bone cancers, malignant mesothelioma, and non-Hodgkin’s lymphoma. Studies are needed to assess current prevalence of SV40 infections.

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 This study was supported in part by the Baylor Center for AIDS Research Core Support Grant AI36211 from the National Institute of Allergy and Infectious Diseases, Bethesda, Maryland. Dr. Vilchez is the recipient of the 2001 Junior Faculty Development Award from GlaxoSmithKline, Philadelphia, Pennsylvania, and the 2002 Translational Research Award from the Leukemia & Lymphoma Society, White Plains, New York. The funding sources had no role in study design; the collection, analysis, or interpretation of data; and the preparation, review, or approval of the manuscript.


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Vol 114 - N° 8

P. 675-684 - juin 2003 Regresar al número
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