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首页> 外文期刊>Oncology letters >Expression of 15-hydroxyprostaglandin dehydrogenase and cyclooxygenase-2 in non-small cell lung cancer: Correlations with angiogenesis and prognosis.
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Expression of 15-hydroxyprostaglandin dehydrogenase and cyclooxygenase-2 in non-small cell lung cancer: Correlations with angiogenesis and prognosis.

机译:非小细胞肺癌中15-羟前列腺素脱氢酶和环氧合酶2的表达:与血管生成和预后的关系。

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摘要

The aim of the present study was to investigate the function of 15-hydroxyprostaglandin dehydrogenase (15-PGDH) and cyclooxygenase-2 (COX-2) in angiogenesis and their association with the prognosis of non-small cell lung cancer (NSCLC). Using immunohistochemical staining, the expression of 15-PGDH and COX-2, and the microvessel density (MVD) levels were evaluated in 35 NSCLC specimens. Paracancerous normal lung tissue was collected as control samples from six patients. The correlation of 15-PGDH with COX-2, clinicopathological characteristics, MVD and overall survival (OS) was studied. NSCLC tissues showed a significantly lower expression level of 15-PGDH (P=0.009) and a significantly higher expression level of COX-2 (P=0.004) compared with normal lung tissue. The expression level of 15-PGDH was negatively correlated with MVD (P<0.001) and COX-2 expression (P=0.032). A low expression level of 15-PGDH, a high expression level of COX-2 and high levels of MVD were significantly correlated with a shorter OS time (15-PGDH, P<0.0001; COX-2, P=0.038; MVD, P<0.0001). This study provided clinical evidence that a low expression level of 15-PGDH is associated with a poor prognosis in NSCLC. Furthermore, it was shown that 15-PGDH and COX-2 reciprocally regulate cancer angiogenesis, which may affect the prognosis of patients with NSCLC.
机译:本研究的目的是研究15-羟基前列腺素脱氢酶(15-PGDH)和环氧合酶2(COX-2)在血管生成中的作用及其与非小细胞肺癌(NSCLC)预后的关系。使用免疫组织化学染色,在35个NSCLC标本中评估了15-PGDH和COX-2的表达以及微血管密度(MVD)水平。从六名患者中收集癌旁正常肺组织作为对照样品。研究了15-PGDH与COX-2,临床病理特征,MVD和总生存期(OS)的相关性。与正常肺组织相比,NSCLC组织显示15-PGDH的表达水平显着较低(P = 0.009),而COX-2的表达水平显着较高(P = 0.004)。 15-PGDH的表达水平与MVD(P <0.001)和COX-2的表达呈负相关(P = 0.032)。 15-PGDH的低表达水平,COX-2的高表达水平和MVD的高水平与较短的OS时间显着相关(15-PGDH,P <0.0001; COX-2,P = 0.038; MVD,P <0.0001)。这项研究提供了临床证据,表明15-PGDH的低表达与NSCLC预后不良有关。此外,已显示15-PGDH和COX-2相互调节癌症血管生成,这可能影响NSCLC患者的预后。

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