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The prognostic significance of UCA1 for predicting clinical outcome in patients with digestive system malignancies

BACKGROUND: Urothelial Carcinoma Associated 1 (UCA1) was an originally identified lncRNA in bladder cancer. Previous studies have reported that UCA1 played a significant role in various types of cancer. This study aimed to clarify the prognostic value of UCA1 in digestive system cancers. RESULTS: Th...

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Autores principales: Liu, Fang-Teng, Dong, Qing, Gao, Hui, Zhu, Zheng-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522294/
https://www.ncbi.nlm.nih.gov/pubmed/28380443
http://dx.doi.org/10.18632/oncotarget.16534
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author Liu, Fang-Teng
Dong, Qing
Gao, Hui
Zhu, Zheng-Ming
author_facet Liu, Fang-Teng
Dong, Qing
Gao, Hui
Zhu, Zheng-Ming
author_sort Liu, Fang-Teng
collection PubMed
description BACKGROUND: Urothelial Carcinoma Associated 1 (UCA1) was an originally identified lncRNA in bladder cancer. Previous studies have reported that UCA1 played a significant role in various types of cancer. This study aimed to clarify the prognostic value of UCA1 in digestive system cancers. RESULTS: The meta-analysis of 15 studies were included, comprising 1441 patients with digestive system cancers. The pooled results of 14 studies indicated that high expression of UCA1 was significantly associated with poorer OS in patients with digestive system cancers (HR: 1.89, 95 % CI: 1.52–2.26). In addition, UCA1 could be as an independent prognostic factor for predicting OS of patients (HR: 1.85, 95 % CI: 1.45–2.25). The pooled results of 3 studies indicated a significant association between UCA1 and DFS in patients with digestive system cancers (HR = 2.50; 95 % CI = 1.30–3.69). Statistical significance was also observed in subgroup meta-analysis. Furthermore, the clinicopathological values of UCA1 were discussed in esophageal cancer, colorectal cancer and pancreatic cancer. MATERIALS AND METHODS: A comprehensive retrieval was performed to search studies evaluating the prognostic value of UCA1 in digestive system cancers. Many databases were involved, including PubMed, Web of Science, Embase and Chinese National Knowledge Infrastructure and Wanfang database. Quantitative meta-analysis was performed with standard statistical methods and the prognostic significance of UCA1 in digestive system cancers was qualified. CONCLUSIONS: Elevated level of UCA1 indicated the poor clinical outcome for patients with digestive system cancers. It may serve as a new biomarker related to prognosis in digestive system cancers.
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spelling pubmed-55222942017-08-21 The prognostic significance of UCA1 for predicting clinical outcome in patients with digestive system malignancies Liu, Fang-Teng Dong, Qing Gao, Hui Zhu, Zheng-Ming Oncotarget Research Paper BACKGROUND: Urothelial Carcinoma Associated 1 (UCA1) was an originally identified lncRNA in bladder cancer. Previous studies have reported that UCA1 played a significant role in various types of cancer. This study aimed to clarify the prognostic value of UCA1 in digestive system cancers. RESULTS: The meta-analysis of 15 studies were included, comprising 1441 patients with digestive system cancers. The pooled results of 14 studies indicated that high expression of UCA1 was significantly associated with poorer OS in patients with digestive system cancers (HR: 1.89, 95 % CI: 1.52–2.26). In addition, UCA1 could be as an independent prognostic factor for predicting OS of patients (HR: 1.85, 95 % CI: 1.45–2.25). The pooled results of 3 studies indicated a significant association between UCA1 and DFS in patients with digestive system cancers (HR = 2.50; 95 % CI = 1.30–3.69). Statistical significance was also observed in subgroup meta-analysis. Furthermore, the clinicopathological values of UCA1 were discussed in esophageal cancer, colorectal cancer and pancreatic cancer. MATERIALS AND METHODS: A comprehensive retrieval was performed to search studies evaluating the prognostic value of UCA1 in digestive system cancers. Many databases were involved, including PubMed, Web of Science, Embase and Chinese National Knowledge Infrastructure and Wanfang database. Quantitative meta-analysis was performed with standard statistical methods and the prognostic significance of UCA1 in digestive system cancers was qualified. CONCLUSIONS: Elevated level of UCA1 indicated the poor clinical outcome for patients with digestive system cancers. It may serve as a new biomarker related to prognosis in digestive system cancers. Impact Journals LLC 2017-03-23 /pmc/articles/PMC5522294/ /pubmed/28380443 http://dx.doi.org/10.18632/oncotarget.16534 Text en Copyright: © 2017 Liu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Liu, Fang-Teng
Dong, Qing
Gao, Hui
Zhu, Zheng-Ming
The prognostic significance of UCA1 for predicting clinical outcome in patients with digestive system malignancies
title The prognostic significance of UCA1 for predicting clinical outcome in patients with digestive system malignancies
title_full The prognostic significance of UCA1 for predicting clinical outcome in patients with digestive system malignancies
title_fullStr The prognostic significance of UCA1 for predicting clinical outcome in patients with digestive system malignancies
title_full_unstemmed The prognostic significance of UCA1 for predicting clinical outcome in patients with digestive system malignancies
title_short The prognostic significance of UCA1 for predicting clinical outcome in patients with digestive system malignancies
title_sort prognostic significance of uca1 for predicting clinical outcome in patients with digestive system malignancies
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522294/
https://www.ncbi.nlm.nih.gov/pubmed/28380443
http://dx.doi.org/10.18632/oncotarget.16534
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