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The association of speckle-type POZ protein with lymph node metastasis and prognosis in cancer patients: A meta-analysis
BACKGROUND: Speckle-type POZ protein (SPOP) has recently been reported as a prognostic tumor biomarker. However, the predictive value of SPOP remains controversial in human cancers. The current meta-analysis was performed to obtain a comprehensive evaluation of the relationship between SPOP expressi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783248/ https://www.ncbi.nlm.nih.gov/pubmed/31577764 http://dx.doi.org/10.1097/MD.0000000000017439 |
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author | Cheng, Fei Zeng, Chunyan Zeng, Ling Wu, Chayan Chen, Youxiang |
author_facet | Cheng, Fei Zeng, Chunyan Zeng, Ling Wu, Chayan Chen, Youxiang |
author_sort | Cheng, Fei |
collection | PubMed |
description | BACKGROUND: Speckle-type POZ protein (SPOP) has recently been reported as a prognostic tumor biomarker. However, the predictive value of SPOP remains controversial in human cancers. The current meta-analysis was performed to obtain a comprehensive evaluation of the relationship between SPOP expression and prognosis of cancer patients. METHODS: Embase, Pubmed, Web of Science, and Chinese Biomedical Literature database were systematically searched up to January 2, 2019. The pooled hazard ratios (HRs) and/or pooled odds ratios (ORs) with 95% confidence intervals (CIs) were used to quantitatively assess the relationship of SPOP expression with prognosis and lymph node metastasis (LNM). RESULTS: A total of 9 studies with 928 patients were included in this meta-analysis. The results showed that low SPOP expression was significantly related to poor overall survival (high/low: HR = 0.55; 95% CI: 0.38–0.79, P = .001), especially for digestive system cancers (high/low: HR = 0.46; 95% CI: 0.27–0.78, P = .003). However, SPOP expression did not affect progression-free survival in cancer patients (high/low: HR = 2.07; 95% CI: 0.16–26.70, P = .578). Additionally, the association between SPOP overexpression and LNM was positive in patients with clear cell renal cell carcinoma (ccRCC) (OR = 5.26; 95% CI: 1.66–16.68, P = .005) but negative in cancer patients without ccRCC (OR = 0.36; 95% CI: 0.21–0.62, P < .001). CONCLUSION: Decreased SPOP expression could predict poor prognosis of cancer patients, suggesting that SPOP protein may be a useful prognostic biomarker in cancer patients. |
format | Online Article Text |
id | pubmed-6783248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-67832482019-11-13 The association of speckle-type POZ protein with lymph node metastasis and prognosis in cancer patients: A meta-analysis Cheng, Fei Zeng, Chunyan Zeng, Ling Wu, Chayan Chen, Youxiang Medicine (Baltimore) 5700 BACKGROUND: Speckle-type POZ protein (SPOP) has recently been reported as a prognostic tumor biomarker. However, the predictive value of SPOP remains controversial in human cancers. The current meta-analysis was performed to obtain a comprehensive evaluation of the relationship between SPOP expression and prognosis of cancer patients. METHODS: Embase, Pubmed, Web of Science, and Chinese Biomedical Literature database were systematically searched up to January 2, 2019. The pooled hazard ratios (HRs) and/or pooled odds ratios (ORs) with 95% confidence intervals (CIs) were used to quantitatively assess the relationship of SPOP expression with prognosis and lymph node metastasis (LNM). RESULTS: A total of 9 studies with 928 patients were included in this meta-analysis. The results showed that low SPOP expression was significantly related to poor overall survival (high/low: HR = 0.55; 95% CI: 0.38–0.79, P = .001), especially for digestive system cancers (high/low: HR = 0.46; 95% CI: 0.27–0.78, P = .003). However, SPOP expression did not affect progression-free survival in cancer patients (high/low: HR = 2.07; 95% CI: 0.16–26.70, P = .578). Additionally, the association between SPOP overexpression and LNM was positive in patients with clear cell renal cell carcinoma (ccRCC) (OR = 5.26; 95% CI: 1.66–16.68, P = .005) but negative in cancer patients without ccRCC (OR = 0.36; 95% CI: 0.21–0.62, P < .001). CONCLUSION: Decreased SPOP expression could predict poor prognosis of cancer patients, suggesting that SPOP protein may be a useful prognostic biomarker in cancer patients. Wolters Kluwer Health 2019-10-04 /pmc/articles/PMC6783248/ /pubmed/31577764 http://dx.doi.org/10.1097/MD.0000000000017439 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 5700 Cheng, Fei Zeng, Chunyan Zeng, Ling Wu, Chayan Chen, Youxiang The association of speckle-type POZ protein with lymph node metastasis and prognosis in cancer patients: A meta-analysis |
title | The association of speckle-type POZ protein with lymph node metastasis and prognosis in cancer patients: A meta-analysis |
title_full | The association of speckle-type POZ protein with lymph node metastasis and prognosis in cancer patients: A meta-analysis |
title_fullStr | The association of speckle-type POZ protein with lymph node metastasis and prognosis in cancer patients: A meta-analysis |
title_full_unstemmed | The association of speckle-type POZ protein with lymph node metastasis and prognosis in cancer patients: A meta-analysis |
title_short | The association of speckle-type POZ protein with lymph node metastasis and prognosis in cancer patients: A meta-analysis |
title_sort | association of speckle-type poz protein with lymph node metastasis and prognosis in cancer patients: a meta-analysis |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783248/ https://www.ncbi.nlm.nih.gov/pubmed/31577764 http://dx.doi.org/10.1097/MD.0000000000017439 |
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