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Clinicopathological and prognostic significance of speckle-type POZ protein in cancers: a systematic review and meta-analysis
BACKGROUND: Controversial findings have been reported in the impact of speckle-type POZ protein (SPOP) on clinicopathological features and prognosis in diverse cancers. We conducted this meta-analysis to confirm whether SPOP was an effective biomarker to predict clinical stage, cancer differentiatio...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8627083/ https://www.ncbi.nlm.nih.gov/pubmed/34838022 http://dx.doi.org/10.1186/s12935-021-02329-5 |
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author | He, Yan Chen, Jun Peng, Xingchen Xia, Yanli Su, Yonglin |
author_facet | He, Yan Chen, Jun Peng, Xingchen Xia, Yanli Su, Yonglin |
author_sort | He, Yan |
collection | PubMed |
description | BACKGROUND: Controversial findings have been reported in the impact of speckle-type POZ protein (SPOP) on clinicopathological features and prognosis in diverse cancers. We conducted this meta-analysis to confirm whether SPOP was an effective biomarker to predict clinical stage, cancer differentiation and survival. METHODS: We searched studies published before June 2021 through Medline, Embase, the Cochrane library register of controlled trials and Wanfang databases. The corrections of SPOP expression with expression disparity, tumor differentiation, clinical stage and survival were analyzed. RESULTS: Our meta-analysis found that higher expression of SPOP was significantly associated with earlier clinical stage, well differentiation and better overall survival. Subgroup analysis showed that the SPOP expression of adjacent tissue was significantly higher than that in cancer tissues of prostate and liver. However, renal cancer presented improved expression of SPOP in cancer tissue. CONCLUSIONS: SPOP has the potential function to act as a novel and effective biomarker for cancer diagnosis and prognostic stratification. |
format | Online Article Text |
id | pubmed-8627083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86270832021-11-30 Clinicopathological and prognostic significance of speckle-type POZ protein in cancers: a systematic review and meta-analysis He, Yan Chen, Jun Peng, Xingchen Xia, Yanli Su, Yonglin Cancer Cell Int Review BACKGROUND: Controversial findings have been reported in the impact of speckle-type POZ protein (SPOP) on clinicopathological features and prognosis in diverse cancers. We conducted this meta-analysis to confirm whether SPOP was an effective biomarker to predict clinical stage, cancer differentiation and survival. METHODS: We searched studies published before June 2021 through Medline, Embase, the Cochrane library register of controlled trials and Wanfang databases. The corrections of SPOP expression with expression disparity, tumor differentiation, clinical stage and survival were analyzed. RESULTS: Our meta-analysis found that higher expression of SPOP was significantly associated with earlier clinical stage, well differentiation and better overall survival. Subgroup analysis showed that the SPOP expression of adjacent tissue was significantly higher than that in cancer tissues of prostate and liver. However, renal cancer presented improved expression of SPOP in cancer tissue. CONCLUSIONS: SPOP has the potential function to act as a novel and effective biomarker for cancer diagnosis and prognostic stratification. BioMed Central 2021-11-27 /pmc/articles/PMC8627083/ /pubmed/34838022 http://dx.doi.org/10.1186/s12935-021-02329-5 Text en © The Author(s) 2021 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review He, Yan Chen, Jun Peng, Xingchen Xia, Yanli Su, Yonglin Clinicopathological and prognostic significance of speckle-type POZ protein in cancers: a systematic review and meta-analysis |
title | Clinicopathological and prognostic significance of speckle-type POZ protein in cancers: a systematic review and meta-analysis |
title_full | Clinicopathological and prognostic significance of speckle-type POZ protein in cancers: a systematic review and meta-analysis |
title_fullStr | Clinicopathological and prognostic significance of speckle-type POZ protein in cancers: a systematic review and meta-analysis |
title_full_unstemmed | Clinicopathological and prognostic significance of speckle-type POZ protein in cancers: a systematic review and meta-analysis |
title_short | Clinicopathological and prognostic significance of speckle-type POZ protein in cancers: a systematic review and meta-analysis |
title_sort | clinicopathological and prognostic significance of speckle-type poz protein in cancers: a systematic review and meta-analysis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8627083/ https://www.ncbi.nlm.nih.gov/pubmed/34838022 http://dx.doi.org/10.1186/s12935-021-02329-5 |
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