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Human cytomegalovirus in high grade serous ovarian cancer possible implications for patients survival

Patients diagnosed with high grade serous ovarian adenocarcinoma have a poor prognosis. Recently human cytomegalovirus (HCMV) has been detected in several tumors. Here, we evaluated HCMV in ovarian cancer tissue specimens obtained at pre- and postchemotherapy tumor resection. Available paraffin embe...

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Autores principales: Carlson, Joseph W., Rådestad, Angelique Flöter, Söderberg-Naucler, Cecilia, Rahbar, Afsar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5794372/
https://www.ncbi.nlm.nih.gov/pubmed/29369188
http://dx.doi.org/10.1097/MD.0000000000009685
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author Carlson, Joseph W.
Rådestad, Angelique Flöter
Söderberg-Naucler, Cecilia
Rahbar, Afsar
author_facet Carlson, Joseph W.
Rådestad, Angelique Flöter
Söderberg-Naucler, Cecilia
Rahbar, Afsar
author_sort Carlson, Joseph W.
collection PubMed
description Patients diagnosed with high grade serous ovarian adenocarcinoma have a poor prognosis. Recently human cytomegalovirus (HCMV) has been detected in several tumors. Here, we evaluated HCMV in ovarian cancer tissue specimens obtained at pre- and postchemotherapy tumor resection. Available paraffin embedded ovarian cancer tissues from matched pre- and postchemotherapy tumor resection specimens (i.e., diagnostic excisional biopsy prechemotherapy; DEBPC) and neoadjuvant chemotherapy followed by interval debulking surgery (NACT + IDS) from 10 patients with stage IIIC-IV high grade serous ovarian carcinoma (HGS) diagnosed between years 2007 and 2008 at Karolinska University Hospital were examined for HCMV immediate-early protein (HCMV-IE), tegument protein pp65, and nucleic acid (β2.7) by immunohistochemistry and in situ hybridization. HCMV-IE and pp65 were detected in 8/10 (80%), 4/9 (44%) and in 4/10 (40%), 5/8 in ovarian cancer tissue specimens from DEBPC and NACT + IDS, respectively. HCMV-β2.7 was detected in all available tissue sections obtained from DEBPC and NACT + IDS. Patients with HCMV-IE or pp65 positive cells in their ovarian tumors at IDS after NACT had a median overall survival of 23.4 and 18.2 months, respectively, compared to 29.6 and 54 months, respectively, in those who did not express HCMV proteins in their tumors. In conclusion, HCMV proteins and nucleic acids are frequently detected at different levels in HGS ovarian carcinoma. Despite the limitation of our study, shorter median overall survival of patients with HCMV-IE and pp65 in their tumor highlights the need to further investigate the role of HCMV in ovarian cancer patients.
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spelling pubmed-57943722018-02-07 Human cytomegalovirus in high grade serous ovarian cancer possible implications for patients survival Carlson, Joseph W. Rådestad, Angelique Flöter Söderberg-Naucler, Cecilia Rahbar, Afsar Medicine (Baltimore) 4900 Patients diagnosed with high grade serous ovarian adenocarcinoma have a poor prognosis. Recently human cytomegalovirus (HCMV) has been detected in several tumors. Here, we evaluated HCMV in ovarian cancer tissue specimens obtained at pre- and postchemotherapy tumor resection. Available paraffin embedded ovarian cancer tissues from matched pre- and postchemotherapy tumor resection specimens (i.e., diagnostic excisional biopsy prechemotherapy; DEBPC) and neoadjuvant chemotherapy followed by interval debulking surgery (NACT + IDS) from 10 patients with stage IIIC-IV high grade serous ovarian carcinoma (HGS) diagnosed between years 2007 and 2008 at Karolinska University Hospital were examined for HCMV immediate-early protein (HCMV-IE), tegument protein pp65, and nucleic acid (β2.7) by immunohistochemistry and in situ hybridization. HCMV-IE and pp65 were detected in 8/10 (80%), 4/9 (44%) and in 4/10 (40%), 5/8 in ovarian cancer tissue specimens from DEBPC and NACT + IDS, respectively. HCMV-β2.7 was detected in all available tissue sections obtained from DEBPC and NACT + IDS. Patients with HCMV-IE or pp65 positive cells in their ovarian tumors at IDS after NACT had a median overall survival of 23.4 and 18.2 months, respectively, compared to 29.6 and 54 months, respectively, in those who did not express HCMV proteins in their tumors. In conclusion, HCMV proteins and nucleic acids are frequently detected at different levels in HGS ovarian carcinoma. Despite the limitation of our study, shorter median overall survival of patients with HCMV-IE and pp65 in their tumor highlights the need to further investigate the role of HCMV in ovarian cancer patients. Wolters Kluwer Health 2018-01-26 /pmc/articles/PMC5794372/ /pubmed/29369188 http://dx.doi.org/10.1097/MD.0000000000009685 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle 4900
Carlson, Joseph W.
Rådestad, Angelique Flöter
Söderberg-Naucler, Cecilia
Rahbar, Afsar
Human cytomegalovirus in high grade serous ovarian cancer possible implications for patients survival
title Human cytomegalovirus in high grade serous ovarian cancer possible implications for patients survival
title_full Human cytomegalovirus in high grade serous ovarian cancer possible implications for patients survival
title_fullStr Human cytomegalovirus in high grade serous ovarian cancer possible implications for patients survival
title_full_unstemmed Human cytomegalovirus in high grade serous ovarian cancer possible implications for patients survival
title_short Human cytomegalovirus in high grade serous ovarian cancer possible implications for patients survival
title_sort human cytomegalovirus in high grade serous ovarian cancer possible implications for patients survival
topic 4900
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5794372/
https://www.ncbi.nlm.nih.gov/pubmed/29369188
http://dx.doi.org/10.1097/MD.0000000000009685
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