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选择性环氧化酶-2抑制剂与氟嘧啶联合治疗结肠癌肝转移

Combined treatment with selective cyclooxygenase-2 inhibitor and fluorinated pyrimidines for liver metastasis of colon cancer.

作者信息

Matsunaga Nobuo, Yamada Nobuya, Ohira Masaichi, Tachimori Akiko, Nishiguchi Yukio, Nishino Hiroji, Seki Syuichi, Hirakawa Kosei

机构信息

Department of Surgical Oncology, Osaka City University, Graduate School of Medicine, 1-4-3 Asahimachi, Abeno-ku, Osaka 545-8585, Japan.

出版信息

Oncol Rep. 2004 Jan;11(1):167-71.

Abstract

Liver metastasis is a major contributor to mortality in patients with colorectal cancer. Hence, it is essential to establish preventive therapy to control liver metastasis. Recently, it has become widely accepted that cyclooxygenase (COX)-2 inhibitors possess anti-cancer activity for various types of tumor, especially colorectal. The clinical application of COX-2 inhibitors may therefore be beneficial. In this study, we have developed a combined treatment with a selective COX-2 inhibitor and fluorinated pyrimidines for liver metastasis of colorectal cancer, and examined the effect of these agents on proliferation and invasion of a highly metastatic human colon cancer cell line, LM-H3. The COX-2 inhibitor etodolac was found to inhibit cell invasion of LM-H3. 5-Fluorouracil (5-FU) inhibited proliferation of this line in vitro. Etodolac did not increase the inhibitory effect of 5-FU on cell proliferation. We also examined the inhibitory effect of etodolac and UFT, belonging to the fluorinated pyrimidines, on liver metastasis by using a liver metastatic model in the nude mouse. Combined treatment with etodolac and UFT markedly reduced liver metastasis. Serious side effects were not observed. In conclusion, combined treatment with etodolac and UFT might be a promising preventive therapy for liver metastasis of colon cancer.

摘要

肝转移是导致结直肠癌患者死亡的主要因素。因此,建立预防肝转移的治疗方法至关重要。近来,环氧化酶(COX)-2抑制剂对多种类型肿瘤尤其是结直肠癌具有抗癌活性这一观点已被广泛接受。因此,COX-2抑制剂的临床应用可能有益。在本研究中,我们开发了一种选择性COX-2抑制剂与氟嘧啶联合治疗结直肠癌肝转移的方法,并研究了这些药物对高转移性人结肠癌细胞系LM-H3增殖和侵袭的影响。发现COX-2抑制剂依托度酸可抑制LM-H3细胞的侵袭。5-氟尿嘧啶(5-FU)在体外可抑制该细胞系的增殖。依托度酸并未增强5-FU对细胞增殖的抑制作用。我们还通过裸鼠肝转移模型研究了依托度酸和属于氟嘧啶类的优福定对肝转移的抑制作用。依托度酸与优福定联合治疗可显著减少肝转移。未观察到严重的副作用。总之,依托度酸与优福定联合治疗可能是一种有前景的结肠癌肝转移预防疗法。

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