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Expression of CD47 in Endometrial Cancer and Its Clinicopathological Significance

PURPOSE: To study the prognostic value of CD47 in endometrial carcinoma (EC) and its correlation with clinicopathological variables. METHODS: Next-generation sequencing data from The Cancer Genome Atlas was analyzed with the Kaplan–Meier curve, Cox's regression model, and ROC curve. A cohort of...

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Autores principales: Yang, Mei, Jiang, Chunfan, Li, Lin, Xing, Hui, Hong, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8916881/
https://www.ncbi.nlm.nih.gov/pubmed/35281519
http://dx.doi.org/10.1155/2022/7188972
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author Yang, Mei
Jiang, Chunfan
Li, Lin
Xing, Hui
Hong, Li
author_facet Yang, Mei
Jiang, Chunfan
Li, Lin
Xing, Hui
Hong, Li
author_sort Yang, Mei
collection PubMed
description PURPOSE: To study the prognostic value of CD47 in endometrial carcinoma (EC) and its correlation with clinicopathological variables. METHODS: Next-generation sequencing data from The Cancer Genome Atlas was analyzed with the Kaplan–Meier curve, Cox's regression model, and ROC curve. A cohort of 544 specimens, including 344 cases of endometrial cancer, 92 cases of endometrial hyperplasia (EH), and 118 cases of normal endometrium (NE), were evaluated with immunohistochemistry and analyzed with statistical methods. RESULTS: For TCGA data, CD47 expression in EC was considerably greater than in NE tissues. CD47 expression correlated significantly with age, clinical stage, histological grade, histological type, and menopause status. Kaplan–Meier analysis and Cox's regression model revealed that elevated CD47 expression was positively correlated with a poorer prognosis. ROC curve showed that CD47 had high specificity and sensitivity as an independent prognosis factor. In our cohort, CD47 expression was significantly stronger in EC than in NE. The strongly positive expression of CD47 could be observed in EC, but none was observed in NE. The CD47 expression rate ranked in descending order: atypical endometrium hyperplasia, complex endometrium hyperplasia, and simple endometrium hyperplasia. Atypical endometrium hyperplasia CD47 expression rate was much greater than either simple endometrium hyperplasia or complex endometrium hyperplasia. A substantial connection existed amongst CD47 expression and the clinical stage. Kaplan–Meier survival analysis demonstrated that CD47 expression was connected with overall survival (OS). Univariate analysis instead of the multivariate analysis revealed that CD47 expression was associated significantly with prognosis. CONCLUSIONS: CD47 is a critical part of the progress of pathogenesis in EC. CD47 expression correlates with multiple clinicopathological variables and is a potential prognostic risk factor.
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spelling pubmed-89168812022-03-12 Expression of CD47 in Endometrial Cancer and Its Clinicopathological Significance Yang, Mei Jiang, Chunfan Li, Lin Xing, Hui Hong, Li J Oncol Research Article PURPOSE: To study the prognostic value of CD47 in endometrial carcinoma (EC) and its correlation with clinicopathological variables. METHODS: Next-generation sequencing data from The Cancer Genome Atlas was analyzed with the Kaplan–Meier curve, Cox's regression model, and ROC curve. A cohort of 544 specimens, including 344 cases of endometrial cancer, 92 cases of endometrial hyperplasia (EH), and 118 cases of normal endometrium (NE), were evaluated with immunohistochemistry and analyzed with statistical methods. RESULTS: For TCGA data, CD47 expression in EC was considerably greater than in NE tissues. CD47 expression correlated significantly with age, clinical stage, histological grade, histological type, and menopause status. Kaplan–Meier analysis and Cox's regression model revealed that elevated CD47 expression was positively correlated with a poorer prognosis. ROC curve showed that CD47 had high specificity and sensitivity as an independent prognosis factor. In our cohort, CD47 expression was significantly stronger in EC than in NE. The strongly positive expression of CD47 could be observed in EC, but none was observed in NE. The CD47 expression rate ranked in descending order: atypical endometrium hyperplasia, complex endometrium hyperplasia, and simple endometrium hyperplasia. Atypical endometrium hyperplasia CD47 expression rate was much greater than either simple endometrium hyperplasia or complex endometrium hyperplasia. A substantial connection existed amongst CD47 expression and the clinical stage. Kaplan–Meier survival analysis demonstrated that CD47 expression was connected with overall survival (OS). Univariate analysis instead of the multivariate analysis revealed that CD47 expression was associated significantly with prognosis. CONCLUSIONS: CD47 is a critical part of the progress of pathogenesis in EC. CD47 expression correlates with multiple clinicopathological variables and is a potential prognostic risk factor. Hindawi 2022-03-04 /pmc/articles/PMC8916881/ /pubmed/35281519 http://dx.doi.org/10.1155/2022/7188972 Text en Copyright © 2022 Mei Yang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yang, Mei
Jiang, Chunfan
Li, Lin
Xing, Hui
Hong, Li
Expression of CD47 in Endometrial Cancer and Its Clinicopathological Significance
title Expression of CD47 in Endometrial Cancer and Its Clinicopathological Significance
title_full Expression of CD47 in Endometrial Cancer and Its Clinicopathological Significance
title_fullStr Expression of CD47 in Endometrial Cancer and Its Clinicopathological Significance
title_full_unstemmed Expression of CD47 in Endometrial Cancer and Its Clinicopathological Significance
title_short Expression of CD47 in Endometrial Cancer and Its Clinicopathological Significance
title_sort expression of cd47 in endometrial cancer and its clinicopathological significance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8916881/
https://www.ncbi.nlm.nih.gov/pubmed/35281519
http://dx.doi.org/10.1155/2022/7188972
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