New developments about the association of SV40 with human mesothelioma

被引:69
作者
Carbone, M
Pass, HI
Miele, L
Bocchetta, M
机构
[1] Loyola Univ, Dept Pathol, Cardinal Bernardin Canc Ctr, Canc Immunol Program, Maywood, IL 60153 USA
[2] Wayne State Univ, Sch Med, Karmanos Canc Ctr, Detroit, MI USA
[3] Univ Illinois, Coll Pharm, Dept Biopharmaceut Sci, Chicago, IL USA
关键词
SV40; mesothelioma; human cancer;
D O I
10.1038/sj.onc.1206552
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Simian virus 40 (SV40) has been detected in human tumors in over 40 different laboratories. Many of these reports linked SV40 to human mesotheliomas. The Vaccine Safety Committee of the Institute of Medicine (IOM), National Academy of Sciences, USA, recently reviewed the evidence associating polio vaccines and/or SV40 with human tumors. The IOM conclusions about polio vaccines and human cancer were: (1) 'the evidence is inadequate to accept or reject a causal relation between SV40-containing polio vaccines and cancer' because the 'epidemiological studies are sufficiently flawed'; (2) 'the biological evidence is of moderate strength that SV40 exposure from the polio vaccines is related to SV40 infection in humans'. The epidemiological studies were considered flawed because it was not possible to distinguish reliably among exposed and nonexposed cohorts. Concerning SV40, the IOM concluded that (1) 'the evidence is strong that SV40 is a transforming virus; (2) the evidence is of moderate strength that SV40 exposure could lead to cancer in humans under natural conditions' (IOM, 2002). Similar conclusions were reached at an International consensus meeting on SV40 and human tumors held at the University of Chicago in 2001. G Klein and C Croce, who chaired the final panel that reviewed all the published evidence linking SV40 to human tumors, stated that 'the presence of SV40 in human tumors has been convincingly demonstrated' (Klein et al, 2002). In addition, a workshop organized by the Biological Carcinogenesis Branch of the National Cancer Institute, Bethesda, MD, chaired by J Pagano, has reached similar conclusions (Wong et aL, 2002). Therefore, three independent scientific panels have all agreed that there is compelling evidence that SV40 is present in some human cancers and that SV40 could contribute to the pathogenesis of some of them. It should be noted that the presence of SV40 in mesothelioma and other human tumor types has been challenged by a research team that has consistently reported negative findings (Strickler et aL, 2001). However, a member of this research team has recently acknowledged - in sworn testimony -sensitivity problems and possible irregularities that raise concerns about these negative reports (MacLachlan, 2002). These revelations, together with the conclusions of the three independent panels mentioned above, appear to bring to an end the apparent controversy about the presence of SV40 in human mesotheliomas and brain tumors.
引用
收藏
页码:5173 / 5180
页数:8
相关论文
共 60 条
[1]   DNA-SEQUENCES SIMILAR TO THOSE OF SIMIAN VIRUS-40 IN EPENDYMOMAS AND CHOROID-PLEXUS TUMORS OF CHILDHOOD [J].
BERGSAGEL, DJ ;
FINEGOLD, MJ ;
BUTEL, JS ;
KUPSKY, WJ ;
GARCEA, RL .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (15) :988-993
[2]   Human mesothelial cells are unusually susceptible to simian virus 40-mediated transformation and asbestos cocarcinogenicity [J].
Bocchetta, M ;
Di Resta, I ;
Powers, A ;
Fresco, R ;
Tosolini, A ;
Testa, JR ;
Pass, HI ;
Rizzo, P ;
Carbone, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (18) :10214-10219
[3]   Notch-1 induction, a novel activity of SV40 required for growth of SV40-transformed human mesothelial cells [J].
Bocchetta, M ;
Miele, L ;
Pass, HI ;
Carbone, M .
ONCOGENE, 2003, 22 (01) :81-89
[4]   Cell and molecular biology of simian virus 40: Implications for human infections and disease [J].
Butel, JS ;
Lednicky, JA .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (02) :119-134
[5]   Viral carcinogenesis: revelation of molecular mechanisms and etiology of human disease [J].
Butel, JS .
CARCINOGENESIS, 2000, 21 (03) :405-426
[6]   SV40 replication in human mesothelial cells induces HGF/Met receptor activation: A model for viral-related carcinogenesis of human malignant mesothelioma [J].
Cacciotti, P ;
Libener, R ;
Betta, P ;
Martini, F ;
Porta, C ;
Procopio, A ;
Strizzi, L ;
Penengo, L ;
Tognon, M ;
Mutti, L ;
Gaudino, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (21) :12032-12037
[7]  
CARBONE M, 1994, ONCOGENE, V9, P1781
[8]   The pathogenesis of mesothelioma [J].
Carbone, M ;
Kratzke, RA ;
Testa, JR .
SEMINARS IN ONCOLOGY, 2002, 29 (01) :2-17
[9]   Simian virus 40, poliovaccines and human tumors: a review of recent developments [J].
Carbone, M ;
Rizzo, P ;
Pass, HI .
ONCOGENE, 1997, 15 (16) :1877-1888
[10]   Simian virus-40 large-T antigen binds p53 in human mesotheliomas [J].
Carbone, M ;
Rizzo, P ;
Grimley, PM ;
Procopio, A ;
Mew, DJY ;
Shridhar, V ;
DeBartolomeis, A ;
Esposito, V ;
Giuliano, MT ;
Steinberg, SM ;
Levine, AS ;
Giordano, A ;
Pass, HI .
NATURE MEDICINE, 1997, 3 (08) :908-912