首页> 外文期刊>Oral oncology >Plasma level of tissue inhibitor of matrix metalloproteinase-1 but not that of matrix metalloproteinase-8 predicts survival in head and neck squamous cell cancer.
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Plasma level of tissue inhibitor of matrix metalloproteinase-1 but not that of matrix metalloproteinase-8 predicts survival in head and neck squamous cell cancer.

机译:基质金属蛋白酶-1的组织抑制剂的血浆水平而非基质金属蛋白酶-8的组织抑制剂的血浆水平预示着头颈部鳞状细胞癌的存活。

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Expression of matrix metalloproteinase-8 (MMP-8) in tongue cancer cells has been associated with an improved prognosis. MMP-8 is inhibited by tissue inhibitor of matrix metalloproteinase-1 (TIMP-1) and elevated levels of TIMP-1 in blood have been associated with poor prognosis in many cancers. We wished to evaluate the usefulness of peripheral blood MMP-8 and TIMP-1 levels as well as the genotypes of MMP8 and TIMP1 in predicting prognosis in head and neck squamous cell carcinoma (HNSCC). Plasma concentrations of MMP-8 and TIMP-1 were analyzed in 136 HNSCC patients. MMP8 and TIMP1 genotypes were determined by analysis of single nucleotide polymorphisms (SNP) in peripheral blood DNA. The mean follow-up time was 3.3years. We found that plasma MMP-8 level did not predict survival but that TIMP-1 level was associated with survival. The adjusted hazard ratio of death scored as a continuous variable on the log(10) scale was 23.2 (95% CI 1.88-286, P=0.01) and that of MMP-8 1.24 (95% CI 0.54-2.84, P=0.61). Immunohistochemical staining showed that TIMP-1 was expressed in vascular endothelium of tumor. TIMP-1 levels were associated with TIMP1 genotype in women but not in men. MMP8 genotype did not correlate with survival or MMP-8 level. Plasma TIMP-1 levels predict survival in HNSCC. TIMP-1 expression is genetically controlled in women. As TIMP-1 inhibits the activity of MMP-8 and it also functions as a growth factor, it may directly influence HNSCC progression.
机译:舌癌细胞中基质金属蛋白酶8(MMP-8)的表达与预后改善有关。 MMP-8被基质金属蛋白酶-1(TIMP-1)的组织抑制剂抑制,血液中TIMP-1的升高与许多癌症的预后不良有关。我们希望评估外周血MMP-8和TIMP-1水平以及MMP8和TIMP1基因型在预测头颈部鳞状细胞癌(HNSCC)预后中的作用。分析了136名HNSCC患者的血浆MMP-8和TIMP-1浓度。通过分析外周血DNA中的单核苷酸多态性(SNP)确定MMP8和TIMP1基因型。平均随访时间为3。3年。我们发现血浆MMP-8水平不能预测生存,但TIMP-1水平与生存有关。在log(10)量表上作为连续变量评分的调整后死亡危险比为23.2(95%CI 1.88-286,P = 0.01)和MMP-8 1.24(95%CI 0.54-2.84,P = 0.61) )。免疫组织化学染色显示TIMP-1在肿瘤的血管内皮中表达。女性中TIMP-1水平与TIMP1基因型相关,而男性则与TIMP1基因型无关。 MMP8基因型与生存率或MMP-8水平无关。血浆TIMP-1水平可预测HNSCC的存活率。女性中TIMP-1的表达受到遗传控制。由于TIMP-1抑制MMP-8的活性,并且还起着生长因子的作用,因此它可能直接影响HNSCC的进程。

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