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Olfactory Receptors as Biomarkers in Human Breast Carcinoma Tissues

Olfactory receptors (ORs) are known to be expressed in a variety of human tissues and act on different physiological processes, such as cell migration, proliferation, or secretion and have been found to function as biomarkers for carcinoma tissues of prostate, lung, and small intestine. In this stud...

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Autores principales: Weber, Lea, Maßberg, Désirée, Becker, Christian, Altmüller, Janine, Ubrig, Burkhard, Bonatz, Gabriele, Wölk, Gerhard, Philippou, Stathis, Tannapfel, Andrea, Hatt, Hanns, Gisselmann, Günter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818398/
https://www.ncbi.nlm.nih.gov/pubmed/29497600
http://dx.doi.org/10.3389/fonc.2018.00033
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author Weber, Lea
Maßberg, Désirée
Becker, Christian
Altmüller, Janine
Ubrig, Burkhard
Bonatz, Gabriele
Wölk, Gerhard
Philippou, Stathis
Tannapfel, Andrea
Hatt, Hanns
Gisselmann, Günter
author_facet Weber, Lea
Maßberg, Désirée
Becker, Christian
Altmüller, Janine
Ubrig, Burkhard
Bonatz, Gabriele
Wölk, Gerhard
Philippou, Stathis
Tannapfel, Andrea
Hatt, Hanns
Gisselmann, Günter
author_sort Weber, Lea
collection PubMed
description Olfactory receptors (ORs) are known to be expressed in a variety of human tissues and act on different physiological processes, such as cell migration, proliferation, or secretion and have been found to function as biomarkers for carcinoma tissues of prostate, lung, and small intestine. In this study, we analyzed the OR expression profiles of several different carcinoma tissues, with a focus on breast cancer. The expression of OR2B6 was detectable in breast carcinoma tissues; here, transcripts of OR2B6 were detected in 73% of all breast carcinoma cell lines and in over 80% of all of the breast carcinoma tissues analyzed. Interestingly, there was no expression of OR2B6 observed in healthy tissues. Immunohistochemical staining of OR2B6 in breast carcinoma tissues revealed a distinct staining pattern of carcinoma cells. Furthermore, we detected a fusion transcript containing part of the coding exon of OR2B6 as a part of a splice variant of the histone HIST1H2BO transcript. In addition, in cancer tissues and cell lines derived from lung, pancreas, and brain, OR expression patterns were compared to that of corresponding healthy tissues. The number of ORs detected in lung carcinoma tissues was significantly reduced in comparison to the surrounding healthy tissues. In pancreatic carcinoma tissues, OR4C6 was considerably more highly expressed in comparison to the respective healthy tissues. We detected OR2B6 as a potential biomarker for breast carcinoma tissues.
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spelling pubmed-58183982018-03-01 Olfactory Receptors as Biomarkers in Human Breast Carcinoma Tissues Weber, Lea Maßberg, Désirée Becker, Christian Altmüller, Janine Ubrig, Burkhard Bonatz, Gabriele Wölk, Gerhard Philippou, Stathis Tannapfel, Andrea Hatt, Hanns Gisselmann, Günter Front Oncol Oncology Olfactory receptors (ORs) are known to be expressed in a variety of human tissues and act on different physiological processes, such as cell migration, proliferation, or secretion and have been found to function as biomarkers for carcinoma tissues of prostate, lung, and small intestine. In this study, we analyzed the OR expression profiles of several different carcinoma tissues, with a focus on breast cancer. The expression of OR2B6 was detectable in breast carcinoma tissues; here, transcripts of OR2B6 were detected in 73% of all breast carcinoma cell lines and in over 80% of all of the breast carcinoma tissues analyzed. Interestingly, there was no expression of OR2B6 observed in healthy tissues. Immunohistochemical staining of OR2B6 in breast carcinoma tissues revealed a distinct staining pattern of carcinoma cells. Furthermore, we detected a fusion transcript containing part of the coding exon of OR2B6 as a part of a splice variant of the histone HIST1H2BO transcript. In addition, in cancer tissues and cell lines derived from lung, pancreas, and brain, OR expression patterns were compared to that of corresponding healthy tissues. The number of ORs detected in lung carcinoma tissues was significantly reduced in comparison to the surrounding healthy tissues. In pancreatic carcinoma tissues, OR4C6 was considerably more highly expressed in comparison to the respective healthy tissues. We detected OR2B6 as a potential biomarker for breast carcinoma tissues. Frontiers Media S.A. 2018-02-15 /pmc/articles/PMC5818398/ /pubmed/29497600 http://dx.doi.org/10.3389/fonc.2018.00033 Text en Copyright © 2018 Weber, Maßberg, Becker, Altmüller, Ubrig, Bonatz, Wölk, Philippou, Tannapfel, Hatt and Gisselmann. 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) and the copyright owner 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
Weber, Lea
Maßberg, Désirée
Becker, Christian
Altmüller, Janine
Ubrig, Burkhard
Bonatz, Gabriele
Wölk, Gerhard
Philippou, Stathis
Tannapfel, Andrea
Hatt, Hanns
Gisselmann, Günter
Olfactory Receptors as Biomarkers in Human Breast Carcinoma Tissues
title Olfactory Receptors as Biomarkers in Human Breast Carcinoma Tissues
title_full Olfactory Receptors as Biomarkers in Human Breast Carcinoma Tissues
title_fullStr Olfactory Receptors as Biomarkers in Human Breast Carcinoma Tissues
title_full_unstemmed Olfactory Receptors as Biomarkers in Human Breast Carcinoma Tissues
title_short Olfactory Receptors as Biomarkers in Human Breast Carcinoma Tissues
title_sort olfactory receptors as biomarkers in human breast carcinoma tissues
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818398/
https://www.ncbi.nlm.nih.gov/pubmed/29497600
http://dx.doi.org/10.3389/fonc.2018.00033
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