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Expression of the luteinizing hormone receptor (LHR) in ovarian cancer
We investigated the association of LHR expression in epithelial ovarian cancer (OC) with clinical and pathologic characteristics of patients. LHR expression was examined immunohistochemically using tissue microarrays (TMAs) of specimens from 232 OC patients. Each sample was scored quantitatively eva...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857310/ https://www.ncbi.nlm.nih.gov/pubmed/31729966 http://dx.doi.org/10.1186/s12885-019-6153-8 |
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author | Xiong, Shigang Mhawech-Fauceglia, Paulette Tsao-Wei, Denice Roman, Lynda Gaur, Rajesh K. Epstein, Alan L. Pinski, Jacek |
author_facet | Xiong, Shigang Mhawech-Fauceglia, Paulette Tsao-Wei, Denice Roman, Lynda Gaur, Rajesh K. Epstein, Alan L. Pinski, Jacek |
author_sort | Xiong, Shigang |
collection | PubMed |
description | We investigated the association of LHR expression in epithelial ovarian cancer (OC) with clinical and pathologic characteristics of patients. LHR expression was examined immunohistochemically using tissue microarrays (TMAs) of specimens from 232 OC patients. Each sample was scored quantitatively evaluating LHR staining intensity (LHR-I) and percentage of LHR (LHR-P) staining cells in tumor cells examined. LHR-I was assessed as no staining (negative), weak (+ 1), moderate (+ 2), and strong positive (+ 3). LHR-P was measured as 1 to 5, 6 to 50% and > 50% of the tumor cells examined. Positive LHR staining was found in 202 (87%) patients’ tumor specimens and 66% patients had strong intensity LHR expression. In 197 (85%) of patients, LHR-P was measured in > 50% of tumor cells. LHR-I was significantly associated with pathologic stage (p = 0.007). We found that 72% of stage III or IV patients expressed strong LHR-I in tumor cells. There were 87% of Silberberg’s grade 2 or 3 patients compared to 70% of grade 1 patients with LHR expression observed in > 50% of tumor cells, p = 0.037. Tumor stage was significantly associated with overall survival and recurrence free survival, p < 0.001 for both analyses, even after adjustment for age, tumor grade and whether patient had persistent disease after therapy or not. Our study demonstrates that LHR is highly expressed in the majority of OC patients. Both LHR-I and LHR-P are significantly associated with either the pathologic stage or tumor grade. |
format | Online Article Text |
id | pubmed-6857310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68573102019-12-05 Expression of the luteinizing hormone receptor (LHR) in ovarian cancer Xiong, Shigang Mhawech-Fauceglia, Paulette Tsao-Wei, Denice Roman, Lynda Gaur, Rajesh K. Epstein, Alan L. Pinski, Jacek BMC Cancer Research Article We investigated the association of LHR expression in epithelial ovarian cancer (OC) with clinical and pathologic characteristics of patients. LHR expression was examined immunohistochemically using tissue microarrays (TMAs) of specimens from 232 OC patients. Each sample was scored quantitatively evaluating LHR staining intensity (LHR-I) and percentage of LHR (LHR-P) staining cells in tumor cells examined. LHR-I was assessed as no staining (negative), weak (+ 1), moderate (+ 2), and strong positive (+ 3). LHR-P was measured as 1 to 5, 6 to 50% and > 50% of the tumor cells examined. Positive LHR staining was found in 202 (87%) patients’ tumor specimens and 66% patients had strong intensity LHR expression. In 197 (85%) of patients, LHR-P was measured in > 50% of tumor cells. LHR-I was significantly associated with pathologic stage (p = 0.007). We found that 72% of stage III or IV patients expressed strong LHR-I in tumor cells. There were 87% of Silberberg’s grade 2 or 3 patients compared to 70% of grade 1 patients with LHR expression observed in > 50% of tumor cells, p = 0.037. Tumor stage was significantly associated with overall survival and recurrence free survival, p < 0.001 for both analyses, even after adjustment for age, tumor grade and whether patient had persistent disease after therapy or not. Our study demonstrates that LHR is highly expressed in the majority of OC patients. Both LHR-I and LHR-P are significantly associated with either the pathologic stage or tumor grade. BioMed Central 2019-11-15 /pmc/articles/PMC6857310/ /pubmed/31729966 http://dx.doi.org/10.1186/s12885-019-6153-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Xiong, Shigang Mhawech-Fauceglia, Paulette Tsao-Wei, Denice Roman, Lynda Gaur, Rajesh K. Epstein, Alan L. Pinski, Jacek Expression of the luteinizing hormone receptor (LHR) in ovarian cancer |
title | Expression of the luteinizing hormone receptor (LHR) in ovarian cancer |
title_full | Expression of the luteinizing hormone receptor (LHR) in ovarian cancer |
title_fullStr | Expression of the luteinizing hormone receptor (LHR) in ovarian cancer |
title_full_unstemmed | Expression of the luteinizing hormone receptor (LHR) in ovarian cancer |
title_short | Expression of the luteinizing hormone receptor (LHR) in ovarian cancer |
title_sort | expression of the luteinizing hormone receptor (lhr) in ovarian cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857310/ https://www.ncbi.nlm.nih.gov/pubmed/31729966 http://dx.doi.org/10.1186/s12885-019-6153-8 |
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