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The clinicopathological significance and prognostic value of EMMPRIN overexpression in cancers: evidence from 39 cohort studies

机译:EMMPRIN过表达在癌症中的临床病理意义和预后价值:来自39个队列研究的证据

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摘要

Extracellular matrix metalloproteinase inducer (EMMPRIN) has been reported to be associated with tumor formation and invasion in many studies. However, the clinicopathological significance and prognosis of EMMPRIN in cancer patients remains inconclusive. Therefore, we conducted a meta-analysis to assess the predictive potential of EMMPRIN in various cancers. By searching Pubmed, Cochrane library database and web of science comprehensively, 39studies with 5739 cases were included in our meta-analysis. The results indicated that EMMPRIN overexpression was significantly associated with poor outcome of cancers (HR=2.46, 95% CI: 2.21-2.75, P<0.0001). In addition, a significant relation was found between EMMPRIN overexpression and clinicopathological features, such as tumor stage (T3+T4/ T1+T2, OR=1.87, 95% CI:1.64-2.12, P<0.0001), tumor differentiation (poor/ well+ moderate, OR=1.09, 95% CI:1.60-2.23, P<0.0001), clinical stage (III+IV /I +II, OR=1.96, 95% CI:1.69-2.27, P<0.0001) and nodal metastasis (positiveegative, OR=2.37, 95% CI:1.93-2.90, P<0.0001). However, the expression of EMMRIN was not significantly associated with tumor stage in cervical cancer (OR=1.35, 95%CI: 0.73-2.48, P=0.33). In conclusion, EMMPRIN overxepression is significantly associated with clinicopathological characteristics and prognosis of cancers. Thus, EMMPRIN may be regarded as a promising bio-marker in predicting the clinical outcome of patients in cancers and could be used as the therapeutic target during clinical practices.
机译:在许多研究中,据报道细胞外基质金属蛋白酶诱导剂(EMMPRIN)与肿瘤的形成和侵袭有关。然而,EMMPRIN在癌症患者中的临床病理学意义和预后仍未定论。因此,我们进行了荟萃分析,以评估EMMPRIN在各种癌症中的预测潜力。通过全面搜索Pubmed,Cochrane图书馆数据库和科学网络,我们的荟萃分析包括39项研究,涉及5739例病例。结果表明,EMMPRIN过表达与癌症的不良预后显着相关(HR = 2.46,95%CI:2.21-2.75,P <0.0001)。此外,发现EMMPRIN过表达与临床病理特征之间存在显着相关性,例如肿瘤分期(T3 + T4 / T1 + T2,OR = 1.87,95%CI:1.64-2.12,P <0.0001),肿瘤分化(差/良好+中度,OR = 1.09,95%CI:1.60-2.23,P <0.0001),临床分期(III + IV / I + II,OR = 1.96,95%CI:1.69-2.27,P <0.0001)和淋巴结转移(正/负,OR = 2.37,95%CI:1.93-2.90,P <0.0001)。然而,EMMRIN的表达与宫颈癌的肿瘤分期没有显着相关性(OR = 1.35,95%CI:0.73-2.48,P = 0.33)。总之,EMMPRIN过表达与临床病理特征和癌症预后显着相关。因此,EMMPRIN可以被认为是预测癌症患者临床结果的有前途的生物标志物,并且可以在临床实践中用作治疗靶标。

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