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Clinical significance of CD133 and Nestin in astrocytic tumor: The correlation with pathological grade and survival

BACKGROUND: We aimed to investigate the interaction between CD133 and Nestin and further assessed the correlation of CD133 and Nestin with clinicopathological characteristics and survival in patients with astrocytic tumor. METHODS: Totally 127 patients with astrocytic tumor underwent surgical resect...

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Autores principales: Zhang, Qingping, Xu, Binchu, Chen, Jianliang, Chen, Furong, Chen, Zhongping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7083417/
https://www.ncbi.nlm.nih.gov/pubmed/31677196
http://dx.doi.org/10.1002/jcla.23082
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author Zhang, Qingping
Xu, Binchu
Chen, Jianliang
Chen, Furong
Chen, Zhongping
author_facet Zhang, Qingping
Xu, Binchu
Chen, Jianliang
Chen, Furong
Chen, Zhongping
author_sort Zhang, Qingping
collection PubMed
description BACKGROUND: We aimed to investigate the interaction between CD133 and Nestin and further assessed the correlation of CD133 and Nestin with clinicopathological characteristics and survival in patients with astrocytic tumor. METHODS: Totally 127 patients with astrocytic tumor underwent surgical resection were enrolled. Patients’ age, gender, and World Health Organization (WHO) grade were recorded, and the survival data were extracted from the follow‐up records. The expressions of CD133 and Nestin in astrocytic tumor tissues were analyzed by immunohistochemistry assay. The WHO grade I and II astrocytic tumors were defined as low‐grade astrocytic tumors (LGA), the WHO grade III and IV astrocytic tumors were defined as high‐grade astrocytic tumors (HGA). RESULTS: There were 79 (62.2%), 34 (26.8%), 14 (11.0%), and 0 (0.0%) patients with CD133 negative, low, moderate, and high expression, respectively; 7 (5.5%), 47 (37.0%), 20 (15.7%), 53 (41.7%) patients with Nestin negative, low, moderate, high expression, respectively. CD133 and Nestin were both correlated with advanced WHO grade but not with age or gender, and positive correlation was observed between CD133 and Nestin. For survival, both CD133 and Nestin were correlated with unfavorable overall survival (OS), and further analysis illustrated that Nestin but not CD133 independently predicted poor OS. Subgroup analysis also revealed that Nestin but not CD133 negatively associated with shorter OS in LGA patients, while both CD133 and Nestin were correlated with poor OS in HGA patients. CONCLUSION: CD133 and Nestin present as potential biomarkers for advanced pathological grade and poor survival in patients with astrocytic tumor.
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spelling pubmed-70834172020-03-24 Clinical significance of CD133 and Nestin in astrocytic tumor: The correlation with pathological grade and survival Zhang, Qingping Xu, Binchu Chen, Jianliang Chen, Furong Chen, Zhongping J Clin Lab Anal Research Articles BACKGROUND: We aimed to investigate the interaction between CD133 and Nestin and further assessed the correlation of CD133 and Nestin with clinicopathological characteristics and survival in patients with astrocytic tumor. METHODS: Totally 127 patients with astrocytic tumor underwent surgical resection were enrolled. Patients’ age, gender, and World Health Organization (WHO) grade were recorded, and the survival data were extracted from the follow‐up records. The expressions of CD133 and Nestin in astrocytic tumor tissues were analyzed by immunohistochemistry assay. The WHO grade I and II astrocytic tumors were defined as low‐grade astrocytic tumors (LGA), the WHO grade III and IV astrocytic tumors were defined as high‐grade astrocytic tumors (HGA). RESULTS: There were 79 (62.2%), 34 (26.8%), 14 (11.0%), and 0 (0.0%) patients with CD133 negative, low, moderate, and high expression, respectively; 7 (5.5%), 47 (37.0%), 20 (15.7%), 53 (41.7%) patients with Nestin negative, low, moderate, high expression, respectively. CD133 and Nestin were both correlated with advanced WHO grade but not with age or gender, and positive correlation was observed between CD133 and Nestin. For survival, both CD133 and Nestin were correlated with unfavorable overall survival (OS), and further analysis illustrated that Nestin but not CD133 independently predicted poor OS. Subgroup analysis also revealed that Nestin but not CD133 negatively associated with shorter OS in LGA patients, while both CD133 and Nestin were correlated with poor OS in HGA patients. CONCLUSION: CD133 and Nestin present as potential biomarkers for advanced pathological grade and poor survival in patients with astrocytic tumor. John Wiley and Sons Inc. 2019-11-01 /pmc/articles/PMC7083417/ /pubmed/31677196 http://dx.doi.org/10.1002/jcla.23082 Text en © 2019 The Authors. Journal of Clinical Laboratory Analysis Published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zhang, Qingping
Xu, Binchu
Chen, Jianliang
Chen, Furong
Chen, Zhongping
Clinical significance of CD133 and Nestin in astrocytic tumor: The correlation with pathological grade and survival
title Clinical significance of CD133 and Nestin in astrocytic tumor: The correlation with pathological grade and survival
title_full Clinical significance of CD133 and Nestin in astrocytic tumor: The correlation with pathological grade and survival
title_fullStr Clinical significance of CD133 and Nestin in astrocytic tumor: The correlation with pathological grade and survival
title_full_unstemmed Clinical significance of CD133 and Nestin in astrocytic tumor: The correlation with pathological grade and survival
title_short Clinical significance of CD133 and Nestin in astrocytic tumor: The correlation with pathological grade and survival
title_sort clinical significance of cd133 and nestin in astrocytic tumor: the correlation with pathological grade and survival
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7083417/
https://www.ncbi.nlm.nih.gov/pubmed/31677196
http://dx.doi.org/10.1002/jcla.23082
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