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Can statins lessen the burden of virus mediated cancers?
BACKGROUND: Oncogenic viruses, including hepatitis B virus (HBV), hepatitis C virus (HCV), human papillomavirus (HPV), Epstein Barr virus (EBV), and Kaposi Sarcoma Herpes virus (KSHV) contribute to a significant proportion of the world’s cancers. Given the sizeable burden of virus mediated cancers,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441070/ https://www.ncbi.nlm.nih.gov/pubmed/36058947 http://dx.doi.org/10.1186/s13027-022-00460-0 |
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author | Clark, Eva H. Ahmed, Sarah T. Chang, Elaine Chiao, Elizabeth Y. White, Donna L. |
author_facet | Clark, Eva H. Ahmed, Sarah T. Chang, Elaine Chiao, Elizabeth Y. White, Donna L. |
author_sort | Clark, Eva H. |
collection | PubMed |
description | BACKGROUND: Oncogenic viruses, including hepatitis B virus (HBV), hepatitis C virus (HCV), human papillomavirus (HPV), Epstein Barr virus (EBV), and Kaposi Sarcoma Herpes virus (KSHV) contribute to a significant proportion of the world’s cancers. Given the sizeable burden of virus mediated cancers, development of strategies to prevent and/or treat these cancers is critical. While large population studies suggest that treatment with hydroxymethylglutaryl-CoA reductase inhibitors, commonly known as statins, may reduce the risk of many cancer types including HBV/HCV related hepatocellular carcinoma, few studies have specifically evaluated the impact of statin use in populations at risk for other types of virus mediated cancers. MAIN BODY: Studies of populations with HBV and HCV suggest a protective, dose-dependent effect of statins on hepatocellular carcinoma risk and support the theory that statins may offer clinical benefit if used as chemoprophylactic agents to reduce liver cancer incidence. However, no population level data exists describing the impact of statins on populations with other oncogenic viral infections, such as HPV, EBV, and KSHV. CONCLUSION: Further study of statin use in diverse, global populations with or at high risk for oncogenic viral infections is essential to determine the impact of statin therapy on virus mediated cancer risk. |
format | Online Article Text |
id | pubmed-9441070 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-94410702022-09-05 Can statins lessen the burden of virus mediated cancers? Clark, Eva H. Ahmed, Sarah T. Chang, Elaine Chiao, Elizabeth Y. White, Donna L. Infect Agent Cancer Comment BACKGROUND: Oncogenic viruses, including hepatitis B virus (HBV), hepatitis C virus (HCV), human papillomavirus (HPV), Epstein Barr virus (EBV), and Kaposi Sarcoma Herpes virus (KSHV) contribute to a significant proportion of the world’s cancers. Given the sizeable burden of virus mediated cancers, development of strategies to prevent and/or treat these cancers is critical. While large population studies suggest that treatment with hydroxymethylglutaryl-CoA reductase inhibitors, commonly known as statins, may reduce the risk of many cancer types including HBV/HCV related hepatocellular carcinoma, few studies have specifically evaluated the impact of statin use in populations at risk for other types of virus mediated cancers. MAIN BODY: Studies of populations with HBV and HCV suggest a protective, dose-dependent effect of statins on hepatocellular carcinoma risk and support the theory that statins may offer clinical benefit if used as chemoprophylactic agents to reduce liver cancer incidence. However, no population level data exists describing the impact of statins on populations with other oncogenic viral infections, such as HPV, EBV, and KSHV. CONCLUSION: Further study of statin use in diverse, global populations with or at high risk for oncogenic viral infections is essential to determine the impact of statin therapy on virus mediated cancer risk. BioMed Central 2022-09-04 /pmc/articles/PMC9441070/ /pubmed/36058947 http://dx.doi.org/10.1186/s13027-022-00460-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Comment Clark, Eva H. Ahmed, Sarah T. Chang, Elaine Chiao, Elizabeth Y. White, Donna L. Can statins lessen the burden of virus mediated cancers? |
title | Can statins lessen the burden of virus mediated cancers? |
title_full | Can statins lessen the burden of virus mediated cancers? |
title_fullStr | Can statins lessen the burden of virus mediated cancers? |
title_full_unstemmed | Can statins lessen the burden of virus mediated cancers? |
title_short | Can statins lessen the burden of virus mediated cancers? |
title_sort | can statins lessen the burden of virus mediated cancers? |
topic | Comment |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441070/ https://www.ncbi.nlm.nih.gov/pubmed/36058947 http://dx.doi.org/10.1186/s13027-022-00460-0 |
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