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高BANCR表达与人类恶性肿瘤的较差预后相关:一项更新的系统评价和荟萃分析。

High BANCR expression is associated with worse prognosis in human malignant carcinomas: an updated systematic review and meta-analysis.

作者信息

Fang Shixu, Liu Zhou, Guo Qiang, Chen Cheng, Ke Xixian, Xu Gang

机构信息

Department of Thoracic Surgery, The Affiliated Hospital of Zunyi Medical University, 149 Dalian Road, Zunyi, 563000, Guizhou, China.

出版信息

BMC Cancer. 2020 Sep 9;20(1):870. doi: 10.1186/s12885-020-07177-6.

DOI:10.1186/s12885-020-07177-6
PMID:32907530
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7488167/
Abstract

BACKGROUND

BRAF-activated noncoding RNA (BANCR) is aberrantly expressed in various tumor tissues and has been confirmed to function as a tumor suppressor or oncogene in many types of cancers. Considering the conflicting results and insufficient sampling, a meta-analysis was performed to explore the prognostic value of BANCR in various carcinomas.

METHODS

A comprehensive literature search of PubMed, Web of Science, EMBASE, Cochrane Library and the China National Knowledge Infrastructure (CNKI) was conducted to collect relevant articles.

RESULTS

The pooled results showed a strong relationship between high BANCR expression and poor overall survival (OS) (HR (hazard ratio) =1.60, 95% confidence interval (CI): 1.19-2.15, P = 0.002) and recurrence-free survival (RFS) (HR = 1.53, 95% CI: 1.27-1.85, P < 0.00001). In addition, high BANCR expression predicted advanced tumor stage (OR (odds ratio) =2.39, 95% CI: 1.26-4.53, P = 0.008), presence of lymph node metastasis (OR = 2.03, 95% CI: 1.08-3.83, P = 0.03), positive distant metastasis (OR = 3.08, 95% CI: 1.92-4.96, P < 0.00001) and larger tumor sizes (OR = 1.63, 95% CI: 1.09-2.46, P = 0.02). However, no associations were found for smoking status (OR = 1.01, 95% CI: 0.65-1.56, P = 0.98), age (OR = 0.88, 95% CI: 0.71-1.09, P = 0.236) and sex (OR = 0.91, 95% CI: 0.72-1.16, P = 0.469). The sensitivity analysis of OS showed that the results of each publication were almost consistent with the combined results, and the merged results have high robustness and reliability.

CONCLUSIONS

The results showed that elevated BANCR expression was associated with unfavorable prognosis for most cancer patients, and BANCR could serve as a promising therapeutic target and independent prognostic predictor in most of cancer types.

摘要

背景

BRAF激活的非编码RNA(BANCR)在多种肿瘤组织中异常表达,并且在多种癌症类型中已被证实发挥肿瘤抑制因子或癌基因的作用。鉴于结果相互矛盾且样本量不足,进行了一项荟萃分析以探讨BANCR在各种癌症中的预后价值。

方法

对PubMed、Web of Science、EMBASE、Cochrane图书馆和中国知网(CNKI)进行全面的文献检索,以收集相关文章。

结果

汇总结果显示,BANCR高表达与总生存期(OS)较差(风险比(HR)=1.60,95%置信区间(CI):1.19 - 2.15,P = 0.002)和无复发生存期(RFS)较差(HR = 1.53,95% CI:1.27 - 1.85,P < 0.00001)之间存在密切关系。此外,BANCR高表达预示着肿瘤分期较晚(优势比(OR)=2.39,95% CI:1.26 - 4.53,P = 0.008)、存在淋巴结转移(OR = 2.03,95% CI:1.08 - 3.83,P = 0.03)、远处转移阳性(OR = 3.08,95% CI:1.92 - 4.96,P < 0.00001)和肿瘤体积较大(OR = 1.63,95% CI:1.09 - 2.46,P = 0.02)。然而,未发现与吸烟状况(OR = 1.01,95% CI:0.65 - 1.56,P = 0.98)、年龄(OR = 0.88,95% CI:0.71 - 1.09,P = 0.236)和性别(OR = 0.91,95% CI:0.72 - 1.16,P = 0.469)有关联。OS的敏感性分析表明,各出版物的结果与合并结果几乎一致,合并结果具有较高的稳健性和可靠性。

结论

结果表明,BANCR表达升高与大多数癌症患者的不良预后相关,并且BANCR可作为大多数癌症类型中有前景的治疗靶点和独立的预后预测指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/208a72188440/12885_2020_7177_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/2fc438b5c0f7/12885_2020_7177_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/ff31fa5927b1/12885_2020_7177_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/5f505907553b/12885_2020_7177_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/076ea4ee94da/12885_2020_7177_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/27b50aea18ba/12885_2020_7177_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/deda078a526c/12885_2020_7177_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/637f3fc3cfd2/12885_2020_7177_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/208a72188440/12885_2020_7177_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/2fc438b5c0f7/12885_2020_7177_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/ff31fa5927b1/12885_2020_7177_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/5f505907553b/12885_2020_7177_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/076ea4ee94da/12885_2020_7177_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/27b50aea18ba/12885_2020_7177_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/deda078a526c/12885_2020_7177_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/637f3fc3cfd2/12885_2020_7177_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddaf/7488167/208a72188440/12885_2020_7177_Fig8_HTML.jpg

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