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Human Papilloma Viruses and Breast Cancer
PURPOSE: Human papillomaviruses (HPV) may have a role in some breast cancers. The purpose of this study is to fill important gaps in the evidence. These gaps are: (i) confirmation of the presence of high risk for cancer HPVs in breast cancers, (ii) evidence of HPV infections in benign breast tissues...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4679879/ https://www.ncbi.nlm.nih.gov/pubmed/26734565 http://dx.doi.org/10.3389/fonc.2015.00277 |
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author | Lawson, James S. Glenn, Wendy K. Salyakina, Daria Delprado, Warick Clay, Rosemary Antonsson, Annika Heng, Benjamin Miyauchi, Shingo Tran, Dinh D. Ngan, Christopher C. Lutze-Mann, Louise Whitaker, Noel J. |
author_facet | Lawson, James S. Glenn, Wendy K. Salyakina, Daria Delprado, Warick Clay, Rosemary Antonsson, Annika Heng, Benjamin Miyauchi, Shingo Tran, Dinh D. Ngan, Christopher C. Lutze-Mann, Louise Whitaker, Noel J. |
author_sort | Lawson, James S. |
collection | PubMed |
description | PURPOSE: Human papillomaviruses (HPV) may have a role in some breast cancers. The purpose of this study is to fill important gaps in the evidence. These gaps are: (i) confirmation of the presence of high risk for cancer HPVs in breast cancers, (ii) evidence of HPV infections in benign breast tissues prior to the development of HPV-positive breast cancer in the same patients, (iii) evidence that HPVs are biologically active and not harmless passengers in breast cancer. METHODS: RNA-seq data from The Cancer Genome Atlas (TCGA) was used to identify HPV RNA sequences in breast cancers. We also conducted a retrospective cohort study based on polymerase chain reaction (PCR) analyses to identify HPVs in archival specimens from Australian women with benign breast biopsies who later developed breast cancer. To assess whether HPVs in breast cancer were biologically active, the expression of the oncogenic protein HPV E7 was assessed by immunohistochemistry (IHC). RESULTS: Thirty (3.5%) low-risk and 20 (2.3%) high-risk HPV types were identified in 855 breast cancers from the TCGA database. The high risk types were HPV 18 (48%), HPV 113 (24%), HPV 16 (10%), HPV 52 (10%). Data from the PCR cohort study indicated that HPV type 18 was the most common type identified in breast cancer specimens (55% of 40 breast cancer specimens) followed by HPV 16 (13%). The same HPV type was identified in both the benign and subsequent breast cancer in 15 patients. HPV E7 proteins were identified in 72% of benign breast specimens and 59% of invasive breast cancer specimens. CONCLUSION: There were four observations of particular interest: (i) confirmation by both NGS and PCR of the presence of high-risk HPV gene sequences in breast cancers, (ii) a correlation between high-risk HPV in benign breast specimens and subsequent HPV-positive breast cancer in the same patient, (iii) HPVs in breast cancer are likely to be biologically active (as shown by transcription of HPV DNA to RNA plus the expression of HPV E7 proteins), (iv) HPV oncogenic influences may occur early in the development of breast cancer. |
format | Online Article Text |
id | pubmed-4679879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-46798792016-01-05 Human Papilloma Viruses and Breast Cancer Lawson, James S. Glenn, Wendy K. Salyakina, Daria Delprado, Warick Clay, Rosemary Antonsson, Annika Heng, Benjamin Miyauchi, Shingo Tran, Dinh D. Ngan, Christopher C. Lutze-Mann, Louise Whitaker, Noel J. Front Oncol Oncology PURPOSE: Human papillomaviruses (HPV) may have a role in some breast cancers. The purpose of this study is to fill important gaps in the evidence. These gaps are: (i) confirmation of the presence of high risk for cancer HPVs in breast cancers, (ii) evidence of HPV infections in benign breast tissues prior to the development of HPV-positive breast cancer in the same patients, (iii) evidence that HPVs are biologically active and not harmless passengers in breast cancer. METHODS: RNA-seq data from The Cancer Genome Atlas (TCGA) was used to identify HPV RNA sequences in breast cancers. We also conducted a retrospective cohort study based on polymerase chain reaction (PCR) analyses to identify HPVs in archival specimens from Australian women with benign breast biopsies who later developed breast cancer. To assess whether HPVs in breast cancer were biologically active, the expression of the oncogenic protein HPV E7 was assessed by immunohistochemistry (IHC). RESULTS: Thirty (3.5%) low-risk and 20 (2.3%) high-risk HPV types were identified in 855 breast cancers from the TCGA database. The high risk types were HPV 18 (48%), HPV 113 (24%), HPV 16 (10%), HPV 52 (10%). Data from the PCR cohort study indicated that HPV type 18 was the most common type identified in breast cancer specimens (55% of 40 breast cancer specimens) followed by HPV 16 (13%). The same HPV type was identified in both the benign and subsequent breast cancer in 15 patients. HPV E7 proteins were identified in 72% of benign breast specimens and 59% of invasive breast cancer specimens. CONCLUSION: There were four observations of particular interest: (i) confirmation by both NGS and PCR of the presence of high-risk HPV gene sequences in breast cancers, (ii) a correlation between high-risk HPV in benign breast specimens and subsequent HPV-positive breast cancer in the same patient, (iii) HPVs in breast cancer are likely to be biologically active (as shown by transcription of HPV DNA to RNA plus the expression of HPV E7 proteins), (iv) HPV oncogenic influences may occur early in the development of breast cancer. Frontiers Media S.A. 2015-12-16 /pmc/articles/PMC4679879/ /pubmed/26734565 http://dx.doi.org/10.3389/fonc.2015.00277 Text en Copyright © 2015 Lawson, Glenn, Salyakina, Delprado, Clay, Antonsson, Heng, Miyauchi, Tran, Ngan, Lutze-Mann and Whitaker. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Lawson, James S. Glenn, Wendy K. Salyakina, Daria Delprado, Warick Clay, Rosemary Antonsson, Annika Heng, Benjamin Miyauchi, Shingo Tran, Dinh D. Ngan, Christopher C. Lutze-Mann, Louise Whitaker, Noel J. Human Papilloma Viruses and Breast Cancer |
title | Human Papilloma Viruses and Breast Cancer |
title_full | Human Papilloma Viruses and Breast Cancer |
title_fullStr | Human Papilloma Viruses and Breast Cancer |
title_full_unstemmed | Human Papilloma Viruses and Breast Cancer |
title_short | Human Papilloma Viruses and Breast Cancer |
title_sort | human papilloma viruses and breast cancer |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4679879/ https://www.ncbi.nlm.nih.gov/pubmed/26734565 http://dx.doi.org/10.3389/fonc.2015.00277 |
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