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肝细胞癌:使用环氧合酶-2抑制剂进行化学预防是否具有潜力?

Hepatocellular carcinoma: is there a potential for chemoprevention using cyclooxygenase-2 inhibitors?

作者信息

Koga Hironori

机构信息

Second Department of Medicine, and Kurume University Research Center for Innovative Cancer Therapy, Kurume University, Kurume, Japan.

出版信息

Cancer. 2003 Aug 15;98(4):661-7. doi: 10.1002/cncr.11576.

Abstract

Inhibitors of cyclooxygenase-2 (COX-2) have proapoptotic and antiangiogenic effects on malignant tumors and inhibit their invasion to surrounding tissues. These properties are derived from COX-dependent and/or COX-independent signaling via peroxisome proliferator-activated receptor gamma. Although the role of COX-2 involvement in human hepatocarcinogenesis has not been determined yet, selective COX-2 inhibitors with COX-independent properties may potentially suppress hepatocarcinogenesis. This hypothesis should be confirmed in in vivo studies using animal models. These studies may provide insights into any application of the COX-2 inhibitor for primary and/or secondary chemoprevention.

摘要

环氧合酶-2(COX-2)抑制剂对恶性肿瘤具有促凋亡和抗血管生成作用,并能抑制其向周围组织的侵袭。这些特性源于通过过氧化物酶体增殖物激活受体γ的COX依赖性和/或COX非依赖性信号传导。尽管COX-2参与人类肝癌发生的作用尚未确定,但具有COX非依赖性特性的选择性COX-2抑制剂可能潜在地抑制肝癌发生。这一假设应在使用动物模型的体内研究中得到证实。这些研究可能为COX-2抑制剂在原发性和/或继发性化学预防中的任何应用提供见解。

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