首页> 外文期刊>World Journal of Gastroenterology >Expressions of inducible nitric oxide synthase and matrix metalloproteinase-9 and their effects on angiogenesis and progression of hepatocellular carcinoma.
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Expressions of inducible nitric oxide synthase and matrix metalloproteinase-9 and their effects on angiogenesis and progression of hepatocellular carcinoma.

机译:诱导型一氧化氮合酶和基质金属蛋白酶9的表达及其对肝癌血管生成和进展的影响。

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AIM: To determine the expressions of inducible nitric oxide synthase (iNOS) and matrix metalloproteinase-9 (MMP-9) in hepatocellular carcinoma (HCC) and to investigate the relationship between iNOS and MMP-9 expression and their effects on angiogenesis and progression of HCC. METHODS: In this study, we examined iNOS, MMP-9, and CD34 expression in specimens surgically removed from 32 HCC patients and 7 normal liver tissues by immunohistochemical staining. Meanwhile, microvessel density (MVD) was determined as a marker of angiogenesis by counting CD34-positive cells. RESULTS: The positive rates of iNOS and MMP-9 expression were 71.88% (23/32) and 78.13% (25/32) in HCC. MMP-9 expression was significantly correlated with tumor size, capsule status, TNM stage, and risk of HCC recurrence (P = 0.032, P = 0.033, P = 0.007, and P = 0.001, respectively). There was also a significant relationship between iNOS expression and capsule status and risk of HCC recurrence (P = 0.049 and P = 0.004, respectively), but no correlation between iNOS expression and tumor size and TNM stage. There was a positive association between MVD and TNM stage and risk of HCC recurrence (P = 0.037 and P = 0.000, respectively). The count of MVD was significantly different in different iNOS and MMP-9 immunoreactivity groups (F = 17.713 and 17.097, P = 0.000 and P = 0.000, respectively). The examination of Spearman's rank correlation coefficient showed that there was a significant positive correlation between MVD and iNOS, MMP-9 immunoreactivity (r = 0.754 and 0.751, P = 0.000 and P=0.000, respectively). There was also a significant association between MMP-9 and iNOS expression in HCC (P = 0.010). CONCLUSION: Nitric oxide (NO) produced by iNOS could modulate MMP-9 production and therefore contribute to tumor cell angiogenesis and invasion and metastasis in HCC. The strong expression of iNOS and MMP-9 in HCC may be helpful in evaluating the recurrence of HCC, predicting poor prognosis. For patients with strong expression of MMP-9 and iNOS, the optimal treatment scheme needs to be selected.
机译:目的:确定诱导型一氧化氮合酶(iNOS)和基质金属蛋白酶9(MMP-9)在肝细胞癌(HCC)中的表达,探讨iNOS和MMP-9表达之间的关系及其对血管生成和肝癌进展的影响。肝癌方法:在这项研究中,我们通过免疫组织化学染色检查了32例HCC患者和7例正常肝组织的手术标本中iNOS,MMP-9和CD34的表达。同时,通过计数CD34阳性细胞,微血管密度(MVD)被确定为血管生成的标志。结果:肝癌组织中iNOS和MMP-9表达阳性率分别为71.88%(23/32)和78.13%(25/32)。 MMP-9表达与肿瘤大小,囊状状态,TNM分期和HCC复发风险显着相关(分别为P = 0.032,P = 0.033,P = 0.007和P = 0.001)。 iNOS表达与胶囊状态和HCC复发风险之间也存在显着相关性(分别为P = 0.049和P = 0.004),但iNOS表达与肿瘤大小和TNM分期无关。 MVD和TNM分期与HCC复发风险之间存在正相关(分别为P = 0.037和P = 0.000)。在不同的iNOS和MMP-9免疫反应性组中,MVD的计数显着不同(分别为F = 17.713和17.097,P = 0.000和P = 0.000)。 Spearman等级相关系数的检验表明,MVD与iNOS,MMP-9免疫反应性之间存在显着正相关(r分别为0.754和0.751,P = 0.000和P = 0.000)。在肝癌中,MMP-9与iNOS表达之间也存在显着关联(P = 0.010)。结论:iNOS产生的一氧化氮(NO)可以调节MMP-9的产生,从而促进肿瘤细胞的血管生成以及肝癌的侵袭和转移。 iNOS和MMP-9在肝癌中的高表达可能有助于评估肝癌的复发,预后不良。对于MMP-9和iNOS表达强的患者,需要选择最佳治疗方案。

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