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Association between RCAS1 expression and clinical outcome in uterine endometrial cancer

RCAS1, which acts as a ligand for a putative receptor on immune cells such as peripheral lymphocytes and natural killer cells, is strongly expressed in human cancers. RCAS1 can induce these cells to undergo apoptotic cell death, which suggests that RCAS1 expression may prohibit the stromal reaction...

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Autores principales: Sonoda, K, Miyamoto, S, Hirakawa, T, Kaku, T, Nakashima, M, Watanabe, T, Akazawa, K, Fujita, T, Nakano, H
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394364/
https://www.ncbi.nlm.nih.gov/pubmed/12888828
http://dx.doi.org/10.1038/sj.bjc.6601126
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author Sonoda, K
Miyamoto, S
Hirakawa, T
Kaku, T
Nakashima, M
Watanabe, T
Akazawa, K
Fujita, T
Nakano, H
author_facet Sonoda, K
Miyamoto, S
Hirakawa, T
Kaku, T
Nakashima, M
Watanabe, T
Akazawa, K
Fujita, T
Nakano, H
author_sort Sonoda, K
collection PubMed
description RCAS1, which acts as a ligand for a putative receptor on immune cells such as peripheral lymphocytes and natural killer cells, is strongly expressed in human cancers. RCAS1 can induce these cells to undergo apoptotic cell death, which suggests that RCAS1 expression may prohibit the stromal reaction occurring in a tumour. To clarify the clinical significance of RCAS1 expression in uterine endometrial cancer, we analysed the association between RCAS1 expression and clinicopathologic variables by statistical methods. With the use of immunohistochemical techniques, we performed a retrospective study of RCAS1 expression in resected tumour tissue from 147 patients with uterine endometrial cancer. We evaluated the statistical correlation between RCAS1 expression and clinicopathologic variables. RCAS1 was expressed in 106 of 147 patients with uterine endometrial cancer ; 30 of these 147 patients showed RCAS1 overexpression. Overexpression of RCAS1 was significantly correlated with age at surgery, stage, extent of myometrial invasion, and positive peritoneal cytologic results. Multivariate analysis revealed that RCAS1 expression and metastasis were clinically significant prognostic factors for the overall survival. These findings indicated that analysis for RCAS1 expression can provide crucial information about the clinical behaviour of uterine endometrial cancer, which may be valuable for the management of patients with this disease.
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spelling pubmed-23943642009-09-10 Association between RCAS1 expression and clinical outcome in uterine endometrial cancer Sonoda, K Miyamoto, S Hirakawa, T Kaku, T Nakashima, M Watanabe, T Akazawa, K Fujita, T Nakano, H Br J Cancer Molecular and Cellular Pathology RCAS1, which acts as a ligand for a putative receptor on immune cells such as peripheral lymphocytes and natural killer cells, is strongly expressed in human cancers. RCAS1 can induce these cells to undergo apoptotic cell death, which suggests that RCAS1 expression may prohibit the stromal reaction occurring in a tumour. To clarify the clinical significance of RCAS1 expression in uterine endometrial cancer, we analysed the association between RCAS1 expression and clinicopathologic variables by statistical methods. With the use of immunohistochemical techniques, we performed a retrospective study of RCAS1 expression in resected tumour tissue from 147 patients with uterine endometrial cancer. We evaluated the statistical correlation between RCAS1 expression and clinicopathologic variables. RCAS1 was expressed in 106 of 147 patients with uterine endometrial cancer ; 30 of these 147 patients showed RCAS1 overexpression. Overexpression of RCAS1 was significantly correlated with age at surgery, stage, extent of myometrial invasion, and positive peritoneal cytologic results. Multivariate analysis revealed that RCAS1 expression and metastasis were clinically significant prognostic factors for the overall survival. These findings indicated that analysis for RCAS1 expression can provide crucial information about the clinical behaviour of uterine endometrial cancer, which may be valuable for the management of patients with this disease. Nature Publishing Group 2003-08-04 2003-07-29 /pmc/articles/PMC2394364/ /pubmed/12888828 http://dx.doi.org/10.1038/sj.bjc.6601126 Text en Copyright © 2003 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular and Cellular Pathology
Sonoda, K
Miyamoto, S
Hirakawa, T
Kaku, T
Nakashima, M
Watanabe, T
Akazawa, K
Fujita, T
Nakano, H
Association between RCAS1 expression and clinical outcome in uterine endometrial cancer
title Association between RCAS1 expression and clinical outcome in uterine endometrial cancer
title_full Association between RCAS1 expression and clinical outcome in uterine endometrial cancer
title_fullStr Association between RCAS1 expression and clinical outcome in uterine endometrial cancer
title_full_unstemmed Association between RCAS1 expression and clinical outcome in uterine endometrial cancer
title_short Association between RCAS1 expression and clinical outcome in uterine endometrial cancer
title_sort association between rcas1 expression and clinical outcome in uterine endometrial cancer
topic Molecular and Cellular Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394364/
https://www.ncbi.nlm.nih.gov/pubmed/12888828
http://dx.doi.org/10.1038/sj.bjc.6601126
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