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凝血酶是转移性骨桥蛋白阳性肝细胞癌的治疗靶点。

Thrombin is a therapeutic target for metastatic osteopontin-positive hepatocellular carcinoma.

机构信息

Liver Cancer Institute and Zhongshan Hospital, Fudan University, Shanghai, China.

出版信息

Hepatology. 2010 Dec;52(6):2012-22. doi: 10.1002/hep.23942. Epub 2010 Oct 1.

DOI:10.1002/hep.23942
PMID:20890897
Abstract

UNLABELLED

We previously identified osteopontin (OPN) as a promoter and thus a potential therapeutic target for hepatocellular carcinoma (HCC) metastasis. The serine protease thrombin interacts with OPN and can modify its biological activity. To explore the role of thrombin alone or in conjunction with OPN in HCC, we studied the correlation of thrombin levels to HCC prognosis in patients with various OPN levels, and evaluated the effects of OPN fragments generated by thrombin cleavage on proliferation and adhesion of HCC cells. We found that the thrombin level was strongly associated with the metastatic potential of HCC cell lines, and that thrombin was remarkably overexpressed in HCC tissue compared with adjacent nontumor tissue. In addition, HCC tissue from patients with recurrent disease displayed much higher thrombin levels, particularly in those with elevated OPN levels. Only HCCs with elevated OPN levels had a significant correlation between high thrombin levels and overall survival (OS; P < 0.01), or time to recurrence (TTR; P < 0.0001) of HCC. Multivariate analysis revealed that thrombin was an independent prognostic indicator. In vitro assays demonstrated that thrombin promotes the proliferation and adhesion of OPN+ HCC cells. Furthermore, thrombin activated the focal adhesion kinase (FAK) pathway of OPN+ HCC cells, which was blocked by the inhibition of integrin β1.

CONCLUSION

Thrombin plays an important role in OPN-mediated aggressive phenotype of HCC through activation of integrin β1-FAK signaling, and is an independent poor prognostic factor for HCC. Thus, thrombin may be a potential therapeutic target to inhibit HCC metastasis in OPN+ patients.

摘要

未加标签

我们之前发现骨桥蛋白(OPN)是肝癌(HCC)转移的启动子,因此也是潜在的治疗靶点。丝氨酸蛋白酶凝血酶与 OPN 相互作用,并能改变其生物学活性。为了研究凝血酶单独或与 OPN 共同作用在 HCC 中的作用,我们研究了不同 OPN 水平的 HCC 患者中凝血酶水平与 HCC 预后的相关性,并评估了凝血酶切割产生的 OPN 片段对 HCC 细胞增殖和黏附的影响。我们发现凝血酶水平与 HCC 细胞系的转移潜能密切相关,且与相邻非肿瘤组织相比,HCC 组织中凝血酶表达显著上调。此外,复发性疾病患者的 HCC 组织中凝血酶水平更高,尤其是 OPN 水平升高的患者。只有 OPN 水平升高的 HCC 才有较高的凝血酶水平与总生存(OS;P < 0.01)或 HCC 复发时间(TTR;P < 0.0001)之间的显著相关性。多变量分析显示凝血酶是独立的预后指标。体外实验表明凝血酶促进 OPN+ HCC 细胞的增殖和黏附。此外,凝血酶激活了 OPN+ HCC 细胞的粘着斑激酶(FAK)通路,该通路可被整合素 β1 抑制所阻断。

结论

凝血酶通过激活整合素 β1-FAK 信号通路在 OPN 介导的 HCC 侵袭表型中发挥重要作用,是 HCC 的独立不良预后因素。因此,凝血酶可能是抑制 OPN+患者 HCC 转移的潜在治疗靶点。

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