Bae Woom-Yee, Choi Jae-Sun, Kim Ja-Eun, Park Chan, Jeong Joo-Won
Department of Biomedical Science, Graduate School, Kyung Hee University, Seoul, 02447, Republic of Korea.
Department of Anatomy and Neurobiology, School of Medicine, Kyung Hee University, Seoul, 02447, Republic of Korea.
Oncotarget. 2016 Jul 26;7(30):47232-47241. doi: 10.18632/oncotarget.10030.
Angiogenesis is an essential step for tumor survival and progression, and the inhibition of angiogenesis is a good strategy for tumor therapeutics. In this study, we investigated the therapeutic effect of zingerone in a mouse tumor model. Zingerone suppressed tumor progression and tumor angiogenesis. Moreover, we found that zingerone inhibited the angiogenic activities of endothelial cells by both direct and indirect means. A mechanistic study showed that the activities of MMP-2 and MMP-9 in tumor cells were decreased by treatment with zingerone. Interestingly, zingerone-mediated inhibition of MMP-2 and MMP-9 was involved in the JNK pathway. In conclusion, zingerone showed strong anti-angiogenic activity via the inhibition of MMP-2 and MMP-9 during tumor progression, suggesting that zingerone may be a potential therapeutic drug for human cancers.
血管生成是肿瘤存活和进展的关键步骤,抑制血管生成是肿瘤治疗的一种有效策略。在本研究中,我们在小鼠肿瘤模型中研究了姜辣素的治疗效果。姜辣素抑制肿瘤进展和肿瘤血管生成。此外,我们发现姜辣素通过直接和间接方式抑制内皮细胞的血管生成活性。一项机制研究表明,用姜辣素处理可降低肿瘤细胞中MMP-2和MMP-9的活性。有趣的是,姜辣素介导的对MMP-2和MMP-9的抑制作用涉及JNK通路。总之,姜辣素在肿瘤进展过程中通过抑制MMP-2和MMP-9表现出强大的抗血管生成活性,这表明姜辣素可能是一种潜在的人类癌症治疗药物。