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Meta-analysis of associations between telomere length and colorectal cancer survival from observational studies

BACKGROUND: Telomere length (TL) has been reported to be associated with the risk and survival of several cancers. But it is unclear for the prognostic role of TL in colorectal cancer (CRC). MATERIALS AND METHODS: Relevant citations were searched and identified using several major online databases t...

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Autores principales: Wang, Wei, Zheng, Lei, Zhou, Ning, Li, Na, Bulibu, Gilisihan, Xu, Chunlei, Zhang, Yi, Tang, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617524/
https://www.ncbi.nlm.nih.gov/pubmed/28977964
http://dx.doi.org/10.18632/oncotarget.20055
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author Wang, Wei
Zheng, Lei
Zhou, Ning
Li, Na
Bulibu, Gilisihan
Xu, Chunlei
Zhang, Yi
Tang, Yong
author_facet Wang, Wei
Zheng, Lei
Zhou, Ning
Li, Na
Bulibu, Gilisihan
Xu, Chunlei
Zhang, Yi
Tang, Yong
author_sort Wang, Wei
collection PubMed
description BACKGROUND: Telomere length (TL) has been reported to be associated with the risk and survival of several cancers. But it is unclear for the prognostic role of TL in colorectal cancer (CRC). MATERIALS AND METHODS: Relevant citations were searched and identified using several major online databases through April 2017 which investigated associations between TL and CRC prognosis. We combined summary estimates using hazard ratios (HRs) with 95% confidence interval (CI), which were pooled using a random-effects model. Overall survival (OS) was set as the primary outcome of interest. RESULTS: There are 8 cohort studies encompassing 1622 patients included in the meta-analysis. Pooled estimate indicated that long TL was not significantly associated with patient OS (HR 1.26, 95% CI, 0.76 to 2.08). When we conducted subgroup analyses based on baseline charcteristics, we found that long TL (versus short TL) was significantly associated with poor OS in studies conducted in Europe (n = 4, HR 2.73, 95% CI, 1.65 to 4.52, I(2) = 0), using Southern blot to measure TL (n = 3, HR 2.93, 95% CI, 1.69 to 5.10, I(2) = 0) and patients’ age more than 60 years (n = 3, HR 2.65, 95% CI, 1.22 to 5.76, I(2) = 0). We found no significant associations between TL and patient disease-free, recurrence-free or progression-free survival (HR 1.19, 95% CI, 0.45 to 3.15). CONCLUSIONS: Current evidence did not provide solid indication that long TL is significantly associated with improved or poor survival for patients with CRC. Further large sample size prospective cohort studies are warranted to determine the true relationship for specific patients.
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spelling pubmed-56175242017-10-03 Meta-analysis of associations between telomere length and colorectal cancer survival from observational studies Wang, Wei Zheng, Lei Zhou, Ning Li, Na Bulibu, Gilisihan Xu, Chunlei Zhang, Yi Tang, Yong Oncotarget Meta-Analysis BACKGROUND: Telomere length (TL) has been reported to be associated with the risk and survival of several cancers. But it is unclear for the prognostic role of TL in colorectal cancer (CRC). MATERIALS AND METHODS: Relevant citations were searched and identified using several major online databases through April 2017 which investigated associations between TL and CRC prognosis. We combined summary estimates using hazard ratios (HRs) with 95% confidence interval (CI), which were pooled using a random-effects model. Overall survival (OS) was set as the primary outcome of interest. RESULTS: There are 8 cohort studies encompassing 1622 patients included in the meta-analysis. Pooled estimate indicated that long TL was not significantly associated with patient OS (HR 1.26, 95% CI, 0.76 to 2.08). When we conducted subgroup analyses based on baseline charcteristics, we found that long TL (versus short TL) was significantly associated with poor OS in studies conducted in Europe (n = 4, HR 2.73, 95% CI, 1.65 to 4.52, I(2) = 0), using Southern blot to measure TL (n = 3, HR 2.93, 95% CI, 1.69 to 5.10, I(2) = 0) and patients’ age more than 60 years (n = 3, HR 2.65, 95% CI, 1.22 to 5.76, I(2) = 0). We found no significant associations between TL and patient disease-free, recurrence-free or progression-free survival (HR 1.19, 95% CI, 0.45 to 3.15). CONCLUSIONS: Current evidence did not provide solid indication that long TL is significantly associated with improved or poor survival for patients with CRC. Further large sample size prospective cohort studies are warranted to determine the true relationship for specific patients. Impact Journals LLC 2017-08-07 /pmc/articles/PMC5617524/ /pubmed/28977964 http://dx.doi.org/10.18632/oncotarget.20055 Text en Copyright: © 2017 Wang 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 (http://creativecommons.org/licenses/by/3.0/) 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 Meta-Analysis
Wang, Wei
Zheng, Lei
Zhou, Ning
Li, Na
Bulibu, Gilisihan
Xu, Chunlei
Zhang, Yi
Tang, Yong
Meta-analysis of associations between telomere length and colorectal cancer survival from observational studies
title Meta-analysis of associations between telomere length and colorectal cancer survival from observational studies
title_full Meta-analysis of associations between telomere length and colorectal cancer survival from observational studies
title_fullStr Meta-analysis of associations between telomere length and colorectal cancer survival from observational studies
title_full_unstemmed Meta-analysis of associations between telomere length and colorectal cancer survival from observational studies
title_short Meta-analysis of associations between telomere length and colorectal cancer survival from observational studies
title_sort meta-analysis of associations between telomere length and colorectal cancer survival from observational studies
topic Meta-Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617524/
https://www.ncbi.nlm.nih.gov/pubmed/28977964
http://dx.doi.org/10.18632/oncotarget.20055
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