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Cellular localization of nucleolin determines the prognosis in cancers: a meta-analysis
Nucleolin (NCL) is a multifunctional protein expressed in the nucleus, cytoplasm, and cell membrane. Overexpression of NCL has a controversial role as a poor prognostic marker in cancers. In this study, a meta-analysis was performed to evaluate the prognostic value of NCL in different subcellular lo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9329415/ https://www.ncbi.nlm.nih.gov/pubmed/35861882 http://dx.doi.org/10.1007/s00109-022-02228-w |
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author | Yangngam, Supaporn Prasopsiri, Jaturawitt Hatthakarnkul, Phimmada Thongchot, Suyanee Thuwajit, Peti Yenchitsomanus, Pa-thai Edwards, Joanne Thuwajit, Chanitra |
author_facet | Yangngam, Supaporn Prasopsiri, Jaturawitt Hatthakarnkul, Phimmada Thongchot, Suyanee Thuwajit, Peti Yenchitsomanus, Pa-thai Edwards, Joanne Thuwajit, Chanitra |
author_sort | Yangngam, Supaporn |
collection | PubMed |
description | Nucleolin (NCL) is a multifunctional protein expressed in the nucleus, cytoplasm, and cell membrane. Overexpression of NCL has a controversial role as a poor prognostic marker in cancers. In this study, a meta-analysis was performed to evaluate the prognostic value of NCL in different subcellular localizations (cytoplasmic (CyNCL) and nuclear (NuNCL)) across a range of cancers. PubMed was searched for relevant publications. Data were extracted and analyzed from 12 studies involving 1221 patients with eight cancer types. The results revealed high total NCL was significantly associated with poor overall survival (OS) (HR = 2.85 (1.94, 4.91), p < 0.00001, I(2) = 59%) and short disease-free survival (DFS) (HR = 3.57 (2.76, 4.62), p < 0.00001, I(2) = 2%). High CyNCL was significantly associated with poor OS (HR = 4.32 (3.01, 6.19), p < 0.00001, I(2) = 0%) and short DFS (HR = 3.00 (2.17, 4.15), p < 0.00001, I(2) = 0%). In contrast, high NuNCL correlated with increased patient OS (HR = 0.42 (0.20, 0.86), p = 0.02, I(2) = 66%), with no significant correlation to DFS observed (HR = 0.46 (0.19, 1.14), p = 0.09, I(2) = 57%). This study supports the role of subcellular NCL as a poor prognostic cancer biomarker. |
format | Online Article Text |
id | pubmed-9329415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-93294152022-07-29 Cellular localization of nucleolin determines the prognosis in cancers: a meta-analysis Yangngam, Supaporn Prasopsiri, Jaturawitt Hatthakarnkul, Phimmada Thongchot, Suyanee Thuwajit, Peti Yenchitsomanus, Pa-thai Edwards, Joanne Thuwajit, Chanitra J Mol Med (Berl) Review Nucleolin (NCL) is a multifunctional protein expressed in the nucleus, cytoplasm, and cell membrane. Overexpression of NCL has a controversial role as a poor prognostic marker in cancers. In this study, a meta-analysis was performed to evaluate the prognostic value of NCL in different subcellular localizations (cytoplasmic (CyNCL) and nuclear (NuNCL)) across a range of cancers. PubMed was searched for relevant publications. Data were extracted and analyzed from 12 studies involving 1221 patients with eight cancer types. The results revealed high total NCL was significantly associated with poor overall survival (OS) (HR = 2.85 (1.94, 4.91), p < 0.00001, I(2) = 59%) and short disease-free survival (DFS) (HR = 3.57 (2.76, 4.62), p < 0.00001, I(2) = 2%). High CyNCL was significantly associated with poor OS (HR = 4.32 (3.01, 6.19), p < 0.00001, I(2) = 0%) and short DFS (HR = 3.00 (2.17, 4.15), p < 0.00001, I(2) = 0%). In contrast, high NuNCL correlated with increased patient OS (HR = 0.42 (0.20, 0.86), p = 0.02, I(2) = 66%), with no significant correlation to DFS observed (HR = 0.46 (0.19, 1.14), p = 0.09, I(2) = 57%). This study supports the role of subcellular NCL as a poor prognostic cancer biomarker. Springer Berlin Heidelberg 2022-07-21 2022 /pmc/articles/PMC9329415/ /pubmed/35861882 http://dx.doi.org/10.1007/s00109-022-02228-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Yangngam, Supaporn Prasopsiri, Jaturawitt Hatthakarnkul, Phimmada Thongchot, Suyanee Thuwajit, Peti Yenchitsomanus, Pa-thai Edwards, Joanne Thuwajit, Chanitra Cellular localization of nucleolin determines the prognosis in cancers: a meta-analysis |
title | Cellular localization of nucleolin determines the prognosis in cancers: a meta-analysis |
title_full | Cellular localization of nucleolin determines the prognosis in cancers: a meta-analysis |
title_fullStr | Cellular localization of nucleolin determines the prognosis in cancers: a meta-analysis |
title_full_unstemmed | Cellular localization of nucleolin determines the prognosis in cancers: a meta-analysis |
title_short | Cellular localization of nucleolin determines the prognosis in cancers: a meta-analysis |
title_sort | cellular localization of nucleolin determines the prognosis in cancers: a meta-analysis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9329415/ https://www.ncbi.nlm.nih.gov/pubmed/35861882 http://dx.doi.org/10.1007/s00109-022-02228-w |
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