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Prognostic Significance of Cyclin E1 Expression in Patients With Chordoma: A Clinicopathological and Immunohistochemical Study

PURPOSE: Chordomas are rare, slow-growing sarcomas without any accepted prognostic biomarkers. Owing to their proximity to critical neurovascular structures, discovering predictive biomarkers in chordoma has been a significant research effort because it may potentially reduce risky therapies in pati...

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Autores principales: Wei, Ran, Dean, Dylan C., Thanindratarn, Pichaya, Hornicek, Francis J., Guo, Wei, Duan, Zhenfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705258/
https://www.ncbi.nlm.nih.gov/pubmed/33282745
http://dx.doi.org/10.3389/fonc.2020.596330
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author Wei, Ran
Dean, Dylan C.
Thanindratarn, Pichaya
Hornicek, Francis J.
Guo, Wei
Duan, Zhenfeng
author_facet Wei, Ran
Dean, Dylan C.
Thanindratarn, Pichaya
Hornicek, Francis J.
Guo, Wei
Duan, Zhenfeng
author_sort Wei, Ran
collection PubMed
description PURPOSE: Chordomas are rare, slow-growing sarcomas without any accepted prognostic biomarkers. Owing to their proximity to critical neurovascular structures, discovering predictive biomarkers in chordoma has been a significant research effort because it may potentially reduce risky therapies in patients with less aggressive tumors. In response, because cyclin E1 overexpression correlates with patient prognosis in several malignancies, we investigated its expression in chordoma and whether it informs patient prognosis. METHODS: Seventy-five chordoma patient specimens were enrolled in a tissue microarray (TMA) to evaluate cyclin E1 expression via immunohistochemical staining. Western blot was used to assess cyclin E1 expression in chordoma cell lines and fresh tissues. We then correlated cyclin E1 staining intensity in the TMA to clinicopathological features and chordoma patient outcomes. RESULTS: Sixty-three percent of the chordoma patient specimens in the TMA, fifty-six percent of the fresh chordoma tissues, and all chordoma cell lines showed high cyclin E1 expression. In TMA analysis, cyclin E1 expression positively correlated to chordoma patient disease status. By survival analysis, high cyclin E1 expression was an independent prognostic risk factor for chordoma patients along with advanced disease status and positive surgical margin. CONCLUSION: Cyclin E1 is a promising biomarker predicting chordoma patient prognosis.
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spelling pubmed-77052582020-12-03 Prognostic Significance of Cyclin E1 Expression in Patients With Chordoma: A Clinicopathological and Immunohistochemical Study Wei, Ran Dean, Dylan C. Thanindratarn, Pichaya Hornicek, Francis J. Guo, Wei Duan, Zhenfeng Front Oncol Oncology PURPOSE: Chordomas are rare, slow-growing sarcomas without any accepted prognostic biomarkers. Owing to their proximity to critical neurovascular structures, discovering predictive biomarkers in chordoma has been a significant research effort because it may potentially reduce risky therapies in patients with less aggressive tumors. In response, because cyclin E1 overexpression correlates with patient prognosis in several malignancies, we investigated its expression in chordoma and whether it informs patient prognosis. METHODS: Seventy-five chordoma patient specimens were enrolled in a tissue microarray (TMA) to evaluate cyclin E1 expression via immunohistochemical staining. Western blot was used to assess cyclin E1 expression in chordoma cell lines and fresh tissues. We then correlated cyclin E1 staining intensity in the TMA to clinicopathological features and chordoma patient outcomes. RESULTS: Sixty-three percent of the chordoma patient specimens in the TMA, fifty-six percent of the fresh chordoma tissues, and all chordoma cell lines showed high cyclin E1 expression. In TMA analysis, cyclin E1 expression positively correlated to chordoma patient disease status. By survival analysis, high cyclin E1 expression was an independent prognostic risk factor for chordoma patients along with advanced disease status and positive surgical margin. CONCLUSION: Cyclin E1 is a promising biomarker predicting chordoma patient prognosis. Frontiers Media S.A. 2020-11-17 /pmc/articles/PMC7705258/ /pubmed/33282745 http://dx.doi.org/10.3389/fonc.2020.596330 Text en Copyright © 2020 Wei, Dean, Thanindratarn, Hornicek, Guo and Duan 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(s) 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
Wei, Ran
Dean, Dylan C.
Thanindratarn, Pichaya
Hornicek, Francis J.
Guo, Wei
Duan, Zhenfeng
Prognostic Significance of Cyclin E1 Expression in Patients With Chordoma: A Clinicopathological and Immunohistochemical Study
title Prognostic Significance of Cyclin E1 Expression in Patients With Chordoma: A Clinicopathological and Immunohistochemical Study
title_full Prognostic Significance of Cyclin E1 Expression in Patients With Chordoma: A Clinicopathological and Immunohistochemical Study
title_fullStr Prognostic Significance of Cyclin E1 Expression in Patients With Chordoma: A Clinicopathological and Immunohistochemical Study
title_full_unstemmed Prognostic Significance of Cyclin E1 Expression in Patients With Chordoma: A Clinicopathological and Immunohistochemical Study
title_short Prognostic Significance of Cyclin E1 Expression in Patients With Chordoma: A Clinicopathological and Immunohistochemical Study
title_sort prognostic significance of cyclin e1 expression in patients with chordoma: a clinicopathological and immunohistochemical study
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705258/
https://www.ncbi.nlm.nih.gov/pubmed/33282745
http://dx.doi.org/10.3389/fonc.2020.596330
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