Sun Min-Hua, Han Xi-Chun, Jia Ming-Ku, Jiang Wei-Dong, Wang Min, Zhang Hong, Han Gang, Jiang Yi
Department of General Surgery, Second Hospital, Jilin University, Changchun 130041, Jilin Province, China.
World J Gastroenterol. 2005 Oct 14;11(38):5931-7. doi: 10.3748/wjg.v11.i38.5931.
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.
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.
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).
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.
检测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HCC血管生成和进展的影响。
本研究采用免疫组织化学染色法检测32例HCC患者手术切除标本及7例正常肝组织中iNOS、MMP-9和CD34的表达。同时,通过计数CD34阳性细胞来测定微血管密度(MVD)作为血管生成的标志物。
HCC中iNOS和MMP-9表达的阳性率分别为71.88%(23/32)和78.13%(25/32)。MMP-9表达与肿瘤大小、包膜状态、TNM分期及HCC复发风险显著相关(分别为P = 0.032、P = 0.033、P = 0.007和P = 0.001)。iNOS表达与包膜状态及HCC复发风险之间也存在显著关系(分别为P = 0.049和P = 0.004),但iNOS表达与肿瘤大小和TNM分期之间无相关性。MVD与TNM分期及HCC复发风险呈正相关(分别为P = 0.037和P = 0.000)。不同iNOS和MMP-9免疫反应性组的MVD计数有显著差异(F = 17.713和17.097,P = 0.000和P = 0.000)。Spearman等级相关系数检验显示,MVD与iNOS、MMP-9免疫反应性之间存在显著正相关(r = 0.754和0.751,P = 0.000和P = 0.000)。HCC中MMP-9和iNOS表达之间也存在显著关联(P = 0.010)。
iNOS产生的一氧化氮(NO)可调节MMP-9的产生,从而促进HCC中的肿瘤细胞血管生成、侵袭和转移。HCC中iNOS和MMP-9的强表达可能有助于评估HCC的复发,预测预后不良。对于MMP-9和iNOS强表达的患者,需要选择最佳治疗方案。