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死亡相关蛋白激酶表达在肝细胞癌中的预后意义

Prognostic significance of death-associated protein-kinase expression in hepatocellular carcinomas.

作者信息

Matsumoto Hiroshi, Nagao Mitsuo, Ogawa Sanehito, Kanehiro Hiromichi, Hisanaga Michiyoshi, Ko Saiho, Ikeda Naoya, Fujii Hisao, Koyama Fumikazu, Mukogawa Tomohide, Nakajima Yoshiyuki

机构信息

First Department of Surgery, Nara Medical University, 840 Shijo-cho, Kashihara city, Nara 634-8522, Japan.

出版信息

Anticancer Res. 2003 Mar-Apr;23(2B):1333-41.

Abstract

BACKGROUND

Disorder of programmed cell death (PCD) contributes to the pathogenesis and the progression of various cancers. Death-associated protein-kinase(DAP-kinase) was isolated as a positive mediator of apoptosis induced by IFN-gamma. It has been reported that the loss or reduction of DAP-kinase expression was detected in various human tumor cell lines and resulted from methylation of the DAP-kinase gene.

MATERIALS AND METHODS

We investigated the expression of DAP-kinase protein by immunohistochemistry and Western-blotting in 43 patients with hepatocellular carcinoma (HCC). Additionally, we examined the methylation status of the DAP-kinase promoter region by methylation-specific polymerase chain reaction.

RESULTS

In DAP-kinase-positive HCC cases(n = 16), serum AFP levels were lower (p = 0.009), tumor differentiation was higher (p = 0.048), histological portal invasion and metastatic foci were less (p = 0.004 and 0.016, respectively), apoptosis of tumor cells was more (p = 0.0009), and the disease-free survival rate and the overall survival rate were higher (p = 0.0057 and 0.0246, respectively), compared with DAP-kinase-negative cases. The status of DAP-kinase protein expression closely correlated with IFN-gamma-receptor and Fas expression (p = 0.038 and p < 0.0001, respectively), but not the methylation of promoter region.

CONCLUSION

Hepatoma cells may escape from apoptosis through the loss or reduction of DAP-kinase expression, while the block of IFN-gamma signal transduction as well as the methylation of promoter region may reduce the expression of DAP-kinase protein.

摘要

背景

程序性细胞死亡(PCD)紊乱促使多种癌症的发病机制及病情进展。死亡相关蛋白激酶(DAP激酶)作为γ干扰素诱导凋亡的阳性介质被分离出来。据报道,在多种人类肿瘤细胞系中检测到DAP激酶表达缺失或降低,这是由DAP激酶基因甲基化所致。

材料与方法

我们采用免疫组织化学和蛋白质免疫印迹法,对43例肝细胞癌(HCC)患者的DAP激酶蛋白表达进行了研究。此外,我们通过甲基化特异性聚合酶链反应检测了DAP激酶启动子区域的甲基化状态。

结果

与DAP激酶阴性的肝细胞癌病例相比,在DAP激酶阳性的肝细胞癌病例(n = 16)中,血清甲胎蛋白水平较低(p = 0.009),肿瘤分化程度较高(p = 0.048),组织学门静脉侵犯及转移灶较少(分别为p = 0.004和0.016),肿瘤细胞凋亡较多(p = 0.0009),无病生存率和总生存率较高(分别为p = 0.0057和0.0246)。DAP激酶蛋白表达状态与γ干扰素受体和Fas表达密切相关(分别为p = 0.038和p < 0.0001),但与启动子区域甲基化无关。

结论

肝癌细胞可能通过DAP激酶表达缺失或降低而逃避凋亡,而γ干扰素信号转导受阻以及启动子区域甲基化可能会降低DAP激酶蛋白的表达。

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