Cancer stem cell markers predict a poor prognosis in renal cell carcinoma: a meta-analysis.

Cancer stem cell markers predict a poor prognosis in renal cell carcinoma: a meta-analysis.
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DOI:
10.18632/oncotarget.11672
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发表时间:
2016-10-04
期刊:
影响因子:
--
通讯作者:
Qiu X
Qiu X
中科院分区:
其他
文献类型:
--
作者:
Cheng B;Yang G;Jiang R;Cheng Y;Yang H;Pei L;Qiu X

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肿瘤干细胞相关标志物可作为肾细胞癌预后的生物标志物。然而,它们的实际预后意义仍然没有定论。因此,进行荟萃分析以更准确地重新评估CSC相关标志物(CXCR 4、CD 133、CD 44、CD 105)表达与RCC预后的相关性。检索PubMed和Embase以寻找合格的研究。合并的风险比(HR)和95%置信区间(95%CI)用于重新评估CSC标志物表达与RCC预后(总生存期(OS)、癌症特异性生存期(CSS)、无病生存期(DFS)和无进展生存期(PFS))的相关性。共有25篇相关文章,包括2673例RCC患者,符合荟萃分析的条件。总体汇总分析表明,高CSC标志物表达预测OS(HR,2.10,95% CI:1.73-2.55)和DFS(HR,3.77,95% CI:2.30-6.19)较差。CXCR 4高表达预示OS(HR,2.57,95%CI:1.95-3.40)、CSS(HR,1.97,95%CI:1.50-2.59)和DFS(HR,5.82,95%CI:3.01-11.25)较差。在RCC患者中,CD 44过表达与OS(HR,1.58,95%CI:1.14-2.18)、CSS(HR,2.58,95%CI:1.27-5.23)和DFS(HR,4.49,95%CI:2.12-9.53)差相关。CD 133是CSS的独立预后因素(HR,0.4,95%CI:0.29-0.54)。CSC标志物的存在与RCC预后不良相关。CSC可能被潜在地用作RCC患者分层的预后标志物,也可能代表新的潜在治疗靶点。
Relevant markers of CSCs may serve as prognostic biomarkers of RCC. However, their actual prognostic significance remains inconclusive. Thus, a meta-analysis was performed to reevaluate the association of CSCs-relevant markers (CXCR4, CD133, CD44, CD105) expression with RCC prognosis more precisely. PubMed and Embase were searched to look for eligible studies. The pooled hazard ratios (HR) with 95% confidence intervals (95% CI) were used to reassess the association of CSCs markers expression and RCC prognosis of overall survival (OS), cancer-specific survival (CSS), disease-free survival (DFS), and progression-free survival (PFS). There were 25 relevant articles, encompassing 2673 RCC patients, eligible for meta-analysis. Overall pooled analysis suggested that high CSCs markers expression predicted poor OS (HR, 2.10, 95% CI: 1.73–2.55) and DFS (HR, 3.77, 95% CI: 2.30–6.19). High CXCR4 expression predicted worse OS (HR, 2.57, 95% CI: 1.95–3.40), CSS (HR,1.97, 95% CI: 1.50–2.59), and DFS (HR, 5.82, 95% CI: 3.01–11.25). CD44 over-expression correlated with a poor OS(HR,1.58, 95% CI: 1.14–2.18), CSS (HR, 2.58, 95% CI: 1.27–5.23), and DFS (HR, 4.49, 95% CI: 2.12–9.53) in RCC patients. CD133 was an independent favorable prognostic factor for CSS (HR, 0.4, 95% CI: 0.29–0.54). The presence of CSCs markers correlates with poor RCC outcome. CSCs may be potentially utilized as prognostic markers to stratify RCC patients, probably representing also a novel potential therapeutic target.