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Detection of human cytomegalovirus in normal and neoplastic breast epithelium

INTRODUCTION: Human cytomegalovirus (HCMV) establishes a persistent life-long infection, and can cause severe pathology in the fetus and the immunocompromised host[1]. Breast milk is the primary route of transmission in humans worldwide, and breast epithelium is thus a likely site of persistent infe...

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Autores principales: Harkins, Lualhati E, Matlaf, Lisa A, Soroceanu, Liliana, Klemm, Katrin, Britt, William J, Wang, Wenquan, Bland, Kirby I, Cobbs, Charles S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3063230/
https://www.ncbi.nlm.nih.gov/pubmed/21429243
http://dx.doi.org/10.1186/2042-4280-1-8
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author Harkins, Lualhati E
Matlaf, Lisa A
Soroceanu, Liliana
Klemm, Katrin
Britt, William J
Wang, Wenquan
Bland, Kirby I
Cobbs, Charles S
author_facet Harkins, Lualhati E
Matlaf, Lisa A
Soroceanu, Liliana
Klemm, Katrin
Britt, William J
Wang, Wenquan
Bland, Kirby I
Cobbs, Charles S
author_sort Harkins, Lualhati E
collection PubMed
description INTRODUCTION: Human cytomegalovirus (HCMV) establishes a persistent life-long infection, and can cause severe pathology in the fetus and the immunocompromised host[1]. Breast milk is the primary route of transmission in humans worldwide, and breast epithelium is thus a likely site of persistent infection and/or reactivation, though this phenomenon has not previously been demonstrated. Increasing evidence indicates HCMV infection can modulate signaling pathways associated with oncogenesis. We hypothesized that persistent HCMV infection occurs in normal adult breast epithelium and that persistent viral expression might be associated with normal and neoplastic ductal epithelium. METHODS: Surgical biopsy specimens of normal breast (n = 38) breast carcinoma (n = 39) and paired normal breast from breast cancer patients (n = 21) were obtained. Specimens were evaluated by immunohistochemistry, in situ hybridization, PCR and DNA sequencing for evidence of HCMV antigens and nucleic acids. RESULTS: We detected HCMV expression specifically in glandular epithelium in 17/27 (63%) of normal adult breast cases evaluated. In contrast, HCMV expression was evident in the neoplastic epithelium of 31/32 (97%) patients with ductal carcinoma in situ (DCIS) and infiltrating ductal carcinoma (IDC) cases evaluated (p = 0.0009). CONCLUSIONS: These findings are the first to demonstrate that persistent HCMV infection occurs in breast epithelium in a significant percentage of normal adult females. HCMV expression was also evident in neoplastic breast epithelium in a high percentage of normal and neoplastic breast tissues obtained from breast cancer patients, raising the possibility that viral infection may be involved in the neoplastic process.
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spelling pubmed-30632302011-03-24 Detection of human cytomegalovirus in normal and neoplastic breast epithelium Harkins, Lualhati E Matlaf, Lisa A Soroceanu, Liliana Klemm, Katrin Britt, William J Wang, Wenquan Bland, Kirby I Cobbs, Charles S Herpesviridae Research INTRODUCTION: Human cytomegalovirus (HCMV) establishes a persistent life-long infection, and can cause severe pathology in the fetus and the immunocompromised host[1]. Breast milk is the primary route of transmission in humans worldwide, and breast epithelium is thus a likely site of persistent infection and/or reactivation, though this phenomenon has not previously been demonstrated. Increasing evidence indicates HCMV infection can modulate signaling pathways associated with oncogenesis. We hypothesized that persistent HCMV infection occurs in normal adult breast epithelium and that persistent viral expression might be associated with normal and neoplastic ductal epithelium. METHODS: Surgical biopsy specimens of normal breast (n = 38) breast carcinoma (n = 39) and paired normal breast from breast cancer patients (n = 21) were obtained. Specimens were evaluated by immunohistochemistry, in situ hybridization, PCR and DNA sequencing for evidence of HCMV antigens and nucleic acids. RESULTS: We detected HCMV expression specifically in glandular epithelium in 17/27 (63%) of normal adult breast cases evaluated. In contrast, HCMV expression was evident in the neoplastic epithelium of 31/32 (97%) patients with ductal carcinoma in situ (DCIS) and infiltrating ductal carcinoma (IDC) cases evaluated (p = 0.0009). CONCLUSIONS: These findings are the first to demonstrate that persistent HCMV infection occurs in breast epithelium in a significant percentage of normal adult females. HCMV expression was also evident in neoplastic breast epithelium in a high percentage of normal and neoplastic breast tissues obtained from breast cancer patients, raising the possibility that viral infection may be involved in the neoplastic process. BioMed Central 2010-12-23 /pmc/articles/PMC3063230/ /pubmed/21429243 http://dx.doi.org/10.1186/2042-4280-1-8 Text en Copyright ©2010 Harkins et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Harkins, Lualhati E
Matlaf, Lisa A
Soroceanu, Liliana
Klemm, Katrin
Britt, William J
Wang, Wenquan
Bland, Kirby I
Cobbs, Charles S
Detection of human cytomegalovirus in normal and neoplastic breast epithelium
title Detection of human cytomegalovirus in normal and neoplastic breast epithelium
title_full Detection of human cytomegalovirus in normal and neoplastic breast epithelium
title_fullStr Detection of human cytomegalovirus in normal and neoplastic breast epithelium
title_full_unstemmed Detection of human cytomegalovirus in normal and neoplastic breast epithelium
title_short Detection of human cytomegalovirus in normal and neoplastic breast epithelium
title_sort detection of human cytomegalovirus in normal and neoplastic breast epithelium
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3063230/
https://www.ncbi.nlm.nih.gov/pubmed/21429243
http://dx.doi.org/10.1186/2042-4280-1-8
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