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The prognostic value of abnormally expressed lncRNAs in prostatic carcinoma: A systematic review and meta-analysis
Several long noncoding RNAs (lncRNAs) are abnormally expressed in prostate cancer (PCa), suggesting that they could serve as novel prognostic markers. The current meta-analysis was undertaken to better define the prognostic value of various lncRNAs in PCa. The PubMed, Embase, Medline, and Cochrane L...
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Published in: | Medicine (Baltimore) 2017-12, Vol.96 (51), p.e9279-e9279 |
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description | Several long noncoding RNAs (lncRNAs) are abnormally expressed in prostate cancer (PCa), suggesting that they could serve as novel prognostic markers. The current meta-analysis was undertaken to better define the prognostic value of various lncRNAs in PCa.
The PubMed, Embase, Medline, and Cochrane Library databases were systematically searched up to February 19, 2017, to retrieve eligible articles. Outcomes analyzed were biochemical recurrence-free survival (BRFS), overall survival (OS), metastasis-free survival (MFS), and prostate cancer-specific survival (PCSS). Pooled hazard ratios (HRs) and 95% confidence intervals (95%CIs) were calculated using fixed-effects or random-effects models.
A total of 10 studies, evaluating 11 PCa-related lncRNAs, were included in the meta-analysis. Pooled results indicate that the abnormal expression of candidate lncRNAs in PCa samples predicted poor BRFS (HR: 1.67, 95%CI: 1.37-2.04, P |
doi_str_mv | 10.1097/MD.0000000000009279 |
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The PubMed, Embase, Medline, and Cochrane Library databases were systematically searched up to February 19, 2017, to retrieve eligible articles. Outcomes analyzed were biochemical recurrence-free survival (BRFS), overall survival (OS), metastasis-free survival (MFS), and prostate cancer-specific survival (PCSS). Pooled hazard ratios (HRs) and 95% confidence intervals (95%CIs) were calculated using fixed-effects or random-effects models.
A total of 10 studies, evaluating 11 PCa-related lncRNAs, were included in the meta-analysis. Pooled results indicate that the abnormal expression of candidate lncRNAs in PCa samples predicted poor BRFS (HR: 1.67, 95%CI: 1.37-2.04, P < .05), without significant heterogeneity among studies (I = 44%, P = .06). Low PCAT14 expression was negatively associated with OS (HR: 0.66, 95%CI: 0.54-0.79, P < .05), MFS (HR: 0.59, 95%CI: 0.48-0.72, P < .05), and PCSS (HR: 0.50, 95%CI: 0.38-0.66, P < .05). Again, there was no significant heterogeneity among studies. The robustness of our results was confirmed by sensitivity and publication bias analyses.
We conclude that expression analysis of selected lncRNAs may be of prognostic value in PCa patients.</description><identifier>ISSN: 0025-7974</identifier><identifier>EISSN: 1536-5964</identifier><identifier>DOI: 10.1097/MD.0000000000009279</identifier><identifier>PMID: 29390487</identifier><language>eng</language><publisher>United States: The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved</publisher><subject>Aged ; Disease-Free Survival ; Gene Expression Regulation, Neoplastic ; Humans ; Male ; Middle Aged ; Neoplasm Invasiveness - pathology ; Neoplasm Staging ; Prognosis ; Prostatic Neoplasms - genetics ; Prostatic Neoplasms - mortality ; Prostatic Neoplasms - pathology ; Prostatic Neoplasms - therapy ; Risk Assessment ; RNA, Long Noncoding - genetics ; Survival Analysis ; Systematic Review and Meta-Analysis</subject><ispartof>Medicine (Baltimore), 2017-12, Vol.96 (51), p.e9279-e9279</ispartof><rights>The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved.</rights><rights>Copyright © 2017 The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved.</rights><rights>Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2854-48610ff757bf95b97ecc8bf673ec694f0ca3ed6a64c4f80e3de0c29d1a8c1c6d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758189/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758189/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29390487$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Xian-Lan</creatorcontrib><creatorcontrib>Zhang, Ji-Wang</creatorcontrib><creatorcontrib>Li, Bai-Song</creatorcontrib><creatorcontrib>Peng, Shu-Sheng</creatorcontrib><creatorcontrib>Yuan, Yong-Qiang</creatorcontrib><title>The prognostic value of abnormally expressed lncRNAs in prostatic carcinoma: A systematic review and meta-analysis</title><title>Medicine (Baltimore)</title><addtitle>Medicine (Baltimore)</addtitle><description>Several long noncoding RNAs (lncRNAs) are abnormally expressed in prostate cancer (PCa), suggesting that they could serve as novel prognostic markers. The current meta-analysis was undertaken to better define the prognostic value of various lncRNAs in PCa.
The PubMed, Embase, Medline, and Cochrane Library databases were systematically searched up to February 19, 2017, to retrieve eligible articles. Outcomes analyzed were biochemical recurrence-free survival (BRFS), overall survival (OS), metastasis-free survival (MFS), and prostate cancer-specific survival (PCSS). Pooled hazard ratios (HRs) and 95% confidence intervals (95%CIs) were calculated using fixed-effects or random-effects models.
A total of 10 studies, evaluating 11 PCa-related lncRNAs, were included in the meta-analysis. Pooled results indicate that the abnormal expression of candidate lncRNAs in PCa samples predicted poor BRFS (HR: 1.67, 95%CI: 1.37-2.04, P < .05), without significant heterogeneity among studies (I = 44%, P = .06). Low PCAT14 expression was negatively associated with OS (HR: 0.66, 95%CI: 0.54-0.79, P < .05), MFS (HR: 0.59, 95%CI: 0.48-0.72, P < .05), and PCSS (HR: 0.50, 95%CI: 0.38-0.66, P < .05). Again, there was no significant heterogeneity among studies. The robustness of our results was confirmed by sensitivity and publication bias analyses.
We conclude that expression analysis of selected lncRNAs may be of prognostic value in PCa patients.</description><subject>Aged</subject><subject>Disease-Free Survival</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Invasiveness - pathology</subject><subject>Neoplasm Staging</subject><subject>Prognosis</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Prostatic Neoplasms - mortality</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Prostatic Neoplasms - therapy</subject><subject>Risk Assessment</subject><subject>RNA, Long Noncoding - genetics</subject><subject>Survival Analysis</subject><subject>Systematic Review and Meta-Analysis</subject><issn>0025-7974</issn><issn>1536-5964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpdUcFu1DAQtRCIbgtfgIR85JJiO3Ycc0BatRSQ2iKhcrYmzqQbcOzFTnbZvyfbLVXpXEaaee_N6D1C3nB2ypnR76_OT9mjMkKbZ2TBVVkVylTyOVkwJlShjZZH5Djnn4zxUgv5khwJUxoma70g6WaFdJ3ibYh57B3dgJ-Qxo5CE2IawPsdxT_rhDljS31w36-XmfZhz8kj7CkOkutDHOADXdK8yyMOd_OEmx63FEJLBxyhgAB-l_v8irzowGd8fd9PyI-LTzdnX4rLb5-_ni0vCydqJQtZV5x1nVa66YxqjEbn6qardImuMrJjDkpsK6ikk13NsGyROWFaDrXjrmrLE_LxoLuemgFbh2FM4O069QOknY3Q2_83oV_Z27ixSqua12YWeHcvkOLvCfNohz479B4CxilbbmYbjVZKztDyAHWzLTlh93CGM7tPy16d26dpzay3jz984PyLZwbIA2Ab_Ygp__LTFpNdIfhxdaentBGFYFxzIQQr5omW5V_H2KNB</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>Wu, Xian-Lan</creator><creator>Zhang, Ji-Wang</creator><creator>Li, Bai-Song</creator><creator>Peng, Shu-Sheng</creator><creator>Yuan, Yong-Qiang</creator><general>The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved</general><general>Wolters Kluwer Health</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20171201</creationdate><title>The prognostic value of abnormally expressed lncRNAs in prostatic carcinoma: A systematic review and meta-analysis</title><author>Wu, Xian-Lan ; Zhang, Ji-Wang ; Li, Bai-Song ; Peng, Shu-Sheng ; Yuan, Yong-Qiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2854-48610ff757bf95b97ecc8bf673ec694f0ca3ed6a64c4f80e3de0c29d1a8c1c6d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aged</topic><topic>Disease-Free Survival</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasm Invasiveness - pathology</topic><topic>Neoplasm Staging</topic><topic>Prognosis</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Prostatic Neoplasms - mortality</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Prostatic Neoplasms - therapy</topic><topic>Risk Assessment</topic><topic>RNA, Long Noncoding - genetics</topic><topic>Survival Analysis</topic><topic>Systematic Review and Meta-Analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Xian-Lan</creatorcontrib><creatorcontrib>Zhang, Ji-Wang</creatorcontrib><creatorcontrib>Li, Bai-Song</creatorcontrib><creatorcontrib>Peng, Shu-Sheng</creatorcontrib><creatorcontrib>Yuan, Yong-Qiang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Medicine (Baltimore)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Xian-Lan</au><au>Zhang, Ji-Wang</au><au>Li, Bai-Song</au><au>Peng, Shu-Sheng</au><au>Yuan, Yong-Qiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The prognostic value of abnormally expressed lncRNAs in prostatic carcinoma: A systematic review and meta-analysis</atitle><jtitle>Medicine (Baltimore)</jtitle><addtitle>Medicine (Baltimore)</addtitle><date>2017-12-01</date><risdate>2017</risdate><volume>96</volume><issue>51</issue><spage>e9279</spage><epage>e9279</epage><pages>e9279-e9279</pages><issn>0025-7974</issn><eissn>1536-5964</eissn><abstract>Several long noncoding RNAs (lncRNAs) are abnormally expressed in prostate cancer (PCa), suggesting that they could serve as novel prognostic markers. The current meta-analysis was undertaken to better define the prognostic value of various lncRNAs in PCa.
The PubMed, Embase, Medline, and Cochrane Library databases were systematically searched up to February 19, 2017, to retrieve eligible articles. Outcomes analyzed were biochemical recurrence-free survival (BRFS), overall survival (OS), metastasis-free survival (MFS), and prostate cancer-specific survival (PCSS). Pooled hazard ratios (HRs) and 95% confidence intervals (95%CIs) were calculated using fixed-effects or random-effects models.
A total of 10 studies, evaluating 11 PCa-related lncRNAs, were included in the meta-analysis. Pooled results indicate that the abnormal expression of candidate lncRNAs in PCa samples predicted poor BRFS (HR: 1.67, 95%CI: 1.37-2.04, P < .05), without significant heterogeneity among studies (I = 44%, P = .06). Low PCAT14 expression was negatively associated with OS (HR: 0.66, 95%CI: 0.54-0.79, P < .05), MFS (HR: 0.59, 95%CI: 0.48-0.72, P < .05), and PCSS (HR: 0.50, 95%CI: 0.38-0.66, P < .05). Again, there was no significant heterogeneity among studies. The robustness of our results was confirmed by sensitivity and publication bias analyses.
We conclude that expression analysis of selected lncRNAs may be of prognostic value in PCa patients.</abstract><cop>United States</cop><pub>The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved</pub><pmid>29390487</pmid><doi>10.1097/MD.0000000000009279</doi><oa>free_for_read</oa></addata></record> |
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subjects | Aged Disease-Free Survival Gene Expression Regulation, Neoplastic Humans Male Middle Aged Neoplasm Invasiveness - pathology Neoplasm Staging Prognosis Prostatic Neoplasms - genetics Prostatic Neoplasms - mortality Prostatic Neoplasms - pathology Prostatic Neoplasms - therapy Risk Assessment RNA, Long Noncoding - genetics Survival Analysis Systematic Review and Meta-Analysis |
title | The prognostic value of abnormally expressed lncRNAs in prostatic carcinoma: A systematic review and meta-analysis |
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