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Role of simian virus 40 in cancer incidence in solid organ transplant patients
Transplant recipients have an increased risk of developing cancer in comparison with the general population. We present here data on cancer development in transplanted subjects who received organs from donors whose DNA was previously examined for the genomic insertion of Simian Virus 40 (SV40). Acti...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361282/ https://www.ncbi.nlm.nih.gov/pubmed/16622449 http://dx.doi.org/10.1038/sj.bjc.6603107 |
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author | Paracchini, V Costa, A Nanni Garte, S Taioli, E |
author_facet | Paracchini, V Costa, A Nanni Garte, S Taioli, E |
author_sort | Paracchini, V |
collection | PubMed |
description | Transplant recipients have an increased risk of developing cancer in comparison with the general population. We present here data on cancer development in transplanted subjects who received organs from donors whose DNA was previously examined for the genomic insertion of Simian Virus 40 (SV40). Active follow-up of 387 recipients of solid organs donated by 134 donors, not clinically affected by cancer, was performed through the National Transplant Center (NTC). The average length of follow-up after transplant was 671±219 days (range 0–1085 days). Out of 134 proposed donors, 120 were utilised for organ donation. Of these, 12 (10%) were classified as positive for SV40 genomic insertion. None of the 41 recipients of organs from SV40 positive donors developed a tumour during the follow-up. In all, 11 recipients of organs given by SV40 negative donors developed a tumour (cancer incidence: 0.015 per year). In conclusion, cancer rates observed in our study are comparable to what reported by the literature in transplanted patients. Recipients of solid organs from SV40 positive donors do not have an increased risk of cancer after transplant. The role of SV40 in carcinogenesis in transplanted patients may be minimal. |
format | Text |
id | pubmed-2361282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23612822009-09-10 Role of simian virus 40 in cancer incidence in solid organ transplant patients Paracchini, V Costa, A Nanni Garte, S Taioli, E Br J Cancer Genetics and Genomics Transplant recipients have an increased risk of developing cancer in comparison with the general population. We present here data on cancer development in transplanted subjects who received organs from donors whose DNA was previously examined for the genomic insertion of Simian Virus 40 (SV40). Active follow-up of 387 recipients of solid organs donated by 134 donors, not clinically affected by cancer, was performed through the National Transplant Center (NTC). The average length of follow-up after transplant was 671±219 days (range 0–1085 days). Out of 134 proposed donors, 120 were utilised for organ donation. Of these, 12 (10%) were classified as positive for SV40 genomic insertion. None of the 41 recipients of organs from SV40 positive donors developed a tumour during the follow-up. In all, 11 recipients of organs given by SV40 negative donors developed a tumour (cancer incidence: 0.015 per year). In conclusion, cancer rates observed in our study are comparable to what reported by the literature in transplanted patients. Recipients of solid organs from SV40 positive donors do not have an increased risk of cancer after transplant. The role of SV40 in carcinogenesis in transplanted patients may be minimal. Nature Publishing Group 2006-05-22 2006-04-18 /pmc/articles/PMC2361282/ /pubmed/16622449 http://dx.doi.org/10.1038/sj.bjc.6603107 Text en Copyright © 2006 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Genetics and Genomics Paracchini, V Costa, A Nanni Garte, S Taioli, E Role of simian virus 40 in cancer incidence in solid organ transplant patients |
title | Role of simian virus 40 in cancer incidence in solid organ transplant patients |
title_full | Role of simian virus 40 in cancer incidence in solid organ transplant patients |
title_fullStr | Role of simian virus 40 in cancer incidence in solid organ transplant patients |
title_full_unstemmed | Role of simian virus 40 in cancer incidence in solid organ transplant patients |
title_short | Role of simian virus 40 in cancer incidence in solid organ transplant patients |
title_sort | role of simian virus 40 in cancer incidence in solid organ transplant patients |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361282/ https://www.ncbi.nlm.nih.gov/pubmed/16622449 http://dx.doi.org/10.1038/sj.bjc.6603107 |
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