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Tumoral and stromal expression of MMP-2, MMP-9, MMP-14, TIMP-1, TIMP-2, and VEGF-A in cervical cancer patient survival: a competing risk analysis

机译:MMP-2,MMP-9,MMP-14,TIMP-1,TIMP-2和VEGF-A的肿瘤和基质表达在宫颈癌患者存活中:竞争风险分析

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摘要

Abstract Background Expression of matrix metalloproteases 2, 9 and 14 (MMP-2, MMP-9, MMP-14), tissue inhibitors of metalloprotease 1 and 2 (TIMP-1, TIMP-2) and vascular endothelial growth factor A (VEGF-A) is involved in tumor invasion and metastasis via extracellular matrix degradation and angiogenesis. This study aimed to assess whether the expression of MMP-2, MMP-9, MMP-14, TIMP-1, and TIMP-2 in tumors and in the adjacent stroma is associated with cervical cancer prognosis. Methods This study analyzed a retrospective cohort of 64 patients. Protein expression was previously obtained by immunohistochemistry from biopsies containing both tumor and stroma. The expression and percentage of stained cells were categorized as high or low according to the cutoff points by using ROC curves. The follow-up data was collected from diagnosis to the last clinical visit. Clinical status categorized as alive without disease, alive with disease, death due to other causes, and death from the disease. The relative risk of death from the disease was evaluated according to the proteins expression using a cause-specific Cox regression model with a 95% confidence interval (95%CI). For the significant associations (p < 0.05), survival curves of patients with low and high expression were plotted for the competing risk survival curve analyses. Results High expression levels of stromal MMP-2 (RR; 95%CI: 3.91; 1.17–13.02) and stromal TIMP-2 (RR, 95%CI: 8.67; 1.15–65.27) were associated with a greater relative risk of death from the disease and with lower survival (p = 0.03; p = 0.04) than lower expression levels. Low expression levels of stromal MMP-9 (RR, 95%CI: 0.19; 0.05–0.65) and tumoral MMP-9 (HR, 95%CI: 0.19; 0.04–0.90) were protective factors against death from the disease and were associated with poorer survival. Conclusions High expression levels of MMP-2 and TIMP-2 in the stroma were significantly associated with poor survival in cervical cancer patients. High expression of MMP-9 was associated with a favorable cervical cancer prognosis.
机译:摘要背景表达式2,9和14(MMP-2,MMP-9,MMP-14),金属蛋白酶酶组织抑制剂1和2(TIMP-1,TIMP-2)和血管内皮生长因子A(VEGF- a)通过细胞外基质降解和血管生成参与肿瘤侵袭和转移。该研究旨在评估肿瘤和相邻基质中MMP-2,MMP-9,MMP-14,TIMP-1和TIMP-2的表达是否与宫颈癌预后有关。方法本研究分析了64名患者的回顾性队列。先前通过免疫组织化学从含有肿瘤和基质的活组织检查获得的免疫组化获得蛋白质表达。通过使用ROC曲线根据截止点分类染色细胞的表达和百分比。从诊断到最后一次临床访问中收集后续数据。临床状况分类为活着,没有疾病,患有疾病,因其他原因而死亡,以及疾病的死亡。根据使用具有95%置信区间(95%CI)的原因特异性COX回归模型,根据蛋白质表达评估来自该疾病的相对风险。对于重要的关联(P <0.05),绘制了竞争风险存活曲线分析的低表达患者的存活曲线。结果基质MMP-2的高表达水平(RR; 95%CI:3.91; 1.17-13.02)和基质TIMP-2(RR,95%CI:8.67; 1.15-65.27)与来自死亡的更大的相对危险疾病和生存率较低(p = 0.03; p = 0.04)比较低的表达水平。基质MMP-9的低表达水平(RR,95%CI:0.19; 0.05-0.65)和肿瘤MMP-9(HR,95%CI:0.19; 0.04-0.90)是对疾病死亡的保护因素,并与之相关生存较差。结论基质中的MMP-2和TIMP-2的高表达水平与宫颈癌患者的存活差异显着相关。 MMP-9的高表达与有利的宫颈癌预后有关。

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