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转移抑制基因KAI1在黑色素瘤血管生成中的作用。

The role of the metastasis suppressor gene KAI1 in melanoma angiogenesis.

作者信息

Tang Yun, Bhandaru Madhuri, Cheng Yabin, Lu Jing, Li Gang, Ong Christopher J

机构信息

Department of Dermatology and Skin Science, University of British Columbia, Vancouver, BC, Canada.

Department of Pathophysiology, Basic Medical College, Zhengzhou University, Zhengzhou, Henan, China.

出版信息

Pigment Cell Melanoma Res. 2015 Nov;28(6):696-706. doi: 10.1111/pcmr.12399. Epub 2015 Aug 20.

Abstract

The tetraspan protein KAI1 (CD82) has been previously shown to have important roles in cell migration, invasion, and melanoma prognosis. In this study, we investigated the role of KAI1 regarding melanoma angiogenesis. KAI1 overexpression strongly suppressed the growth of the human umbilical vein endothelial cells and their tubular structure formation in vitro. Also, KAI1 was able to inhibit both interleukin-6 (IL-6) and VEGF at mRNA and protein levels. Using nude mice in the in vivo study, we showed that KAI1, through the regulation of ING4, inhibited blood vessel formation in matrigel plugs along with the downregulation of IL-6 and VEGF, and the recruitment of CD31-positive cells. Finally, we found that KAI1 was able to suppress the activity of a serine/threonine kinase Akt by suppressing Akt phosphorylation (Ser473). Taken together, our results suggested that KAI1 was able to suppress melanoma angiogenesis by downregulating IL-6 and VEGF expression, and the restoration of KAI1 functionality offered a new approach in human melanoma treatment.

摘要

四跨膜蛋白KAI1(CD82)先前已被证明在细胞迁移、侵袭和黑色素瘤预后中发挥重要作用。在本研究中,我们调查了KAI1在黑色素瘤血管生成方面的作用。KAI1过表达在体外强烈抑制人脐静脉内皮细胞的生长及其管状结构形成。此外,KAI1能够在mRNA和蛋白质水平上抑制白细胞介素-6(IL-6)和血管内皮生长因子(VEGF)。在体内研究中使用裸鼠,我们发现KAI1通过调节ING4,抑制基质胶栓中的血管形成,同时下调IL-6和VEGF,并减少CD31阳性细胞的募集。最后,我们发现KAI1能够通过抑制Akt磷酸化(Ser473)来抑制丝氨酸/苏氨酸激酶Akt的活性。综上所述,我们的结果表明KAI1能够通过下调IL-6和VEGF表达来抑制黑色素瘤血管生成,恢复KAI1的功能为人类黑色素瘤治疗提供了一种新方法。

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