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Clinicopathological and Prognostic Significance of Cancer Stem Cell Markers in Ovarian Cancer Patients: Evidence from 52 Studies

机译:卵巢癌患者癌症干细胞标记物的临床病理和预后意义:来自52个研究的证据

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Background/Aims Relevant markers of cancer stem cells (CSCs) may serve as commonly used biomarkers of ovarian cancer (OC). However, their actual clinicopathological and prognostic significance remains inconclusive. Thus, we conducted a meta-analysis to quantitatively evaluate the association between the expression of CSC-relevant markers (ALDH1, CD117, CD133, and CD44) and OC. Methods We used an odds ratio (OR) and a hazard ratio (HR) with a 95% confidence interval (CI) to estimate the effects by analyzing 52 studies from a literature search. Heterogeneity and sensitivity were evaluated, as well. Publication bias was assessed using funnel plots and Egger tests. Results ALDH1 expression was statistically associated with FIGO stage (OR=1.872, 95%CI=1.14-3.076, P=0.013) and lymph invasion (OR=2.78, 95%CI=1.08-7.152, P=0.034). CD117 expression was significantly associated with FIGO stage (OR=2.01, 95%CI=1.35-2.98, P=0.001). CD133 expression was correlated with FIGO stage (OR=3.410, 95%CI=2.196-5.294, P< 0.001) and differentiation grade (OR=2.672, 95%CI=1.354-5.272, P=0.005). CD44s was related to chemotherapy resistance (OR=3.218, 95%CI=1.148-9.016, P=0.026). Furthermore, overexpression of ALDH1 (HR=1.494, 95%CI=1.207-1.849, P< 0.001), CD117 (HR=1.395, 95%CI=1.025-1.898, P=0.034) or CD44s (HR=1.725, 95%CI=1.135-2.623, P=0.011) was associated with poor OS. Further, overexpression of both ALDH1 (HR=1.524, 95%CI=1.158-2.007, P=0.003) and CD44s (HR=2.12, 95%CI=1.692-2.657, P< 0.001) was correlated with worse DFS. Conclusion CSC markers are useful predictive or prognostic biomarkers for OC in clinical assessments. Combined detection of CSC marker expression may be a powerful tool for prognostic predictions in clinical practice for patients with OC.
机译:背景/目的癌干细胞(CSCs)的相关标志物可以作为卵巢癌(OC)的常用生物标志物。但是,它们的实际临床病理和预后意义仍然不确定。因此,我们进行了荟萃分析,定量评估CSC相关标志物(ALDH1,CD117,CD133和CD44)的表达与OC之间的关联。方法我们使用95%置信区间(CI)的比值比(OR)和危险比(HR)通过分析来自文献检索的52项研究来估计效果。还评估了异质性和敏感性。使用漏斗图和Egger检验评估出版偏倚。结果ALDH1表达与FIGO分期(OR = 1.872,95%CI = 1.14-3.076,P = 0.013)和淋巴管浸润(OR = 2.78,95%CI = 1.08-7.152,P = 0.034)在统计学上相关。 CD117表达与FIGO阶段显着相关(OR = 2.01,95%CI = 1.35-2.98,P = 0.001)。 CD133表达与FIGO阶段(OR = 3.410,95%CI = 2.196-5.294,P< 0.001)和分化等级(OR = 2.672,95%CI = 1.354-5.272,P = 0.005)相关。 CD44s与化疗耐药有关(OR = 3.218,95%CI = 1.148-9.016,P = 0.026)。此外,ALDH1(HR = 1.494,95%CI = 1.207-1.849,P< 0.001),CD117(HR = 1.395,95%CI = 1.025-1.898,P = 0.034)或CD44s(HR = 1.725, 95%CI = 1.135-2.623,P = 0.011)与OS差有关。此外,ALDH1(HR = 1.524,95%CI = 1.158-2.007,P = 0.003)和CD44s(HR = 2.12,95%CI = 1.692-2.657,P< 0.001)的过表达都与较差的DFS相关。结论CSC标记物是临床评估OC中有用的预测或预后生物标记物。 CSC标志物表达的联合检测可能是用于OC患者临床实践中预后预测的强大工具。

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