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新型合成化合物 TBrC 对高转移性肺癌细胞增殖和迁移的抑制作用及其作用机制。

Suppression of proliferation and migration in highly-metastatic lung cancer cells as well as tumor growth by a new synthesized compound TBrC and its molecular mechanisms of action.

机构信息

Laboratory of Molecular Pharmacology, School of Pharmacy, Yantai University, No. 30, Qing Quan Lu, Lai Shan Qu, Yantai, 264005, Shandong Province, China.

出版信息

Cytotechnology. 2014 Dec;66(6):899-911. doi: 10.1007/s10616-013-9641-8. Epub 2013 Oct 17.

Abstract

To develop new anticancer agents has been considered as a useful and necessary strategy to suppress highly-metastatic lung cancer, the leading cause of cancer-related deaths in the world. In this study, we synthesized a new compound ethyl 6-bromocoumarin-3-carboxylyl L-theanine (TBrC) and studied the anticancer activity of TBrC and its molecular mechanisms of action. Our results show that TBrC remarkably inhibits the proliferation and migration in highly-metastatic lung cancer cells by inducing apoptosis and cell cycle arrest as well as regulating related protein expressions. Further study indicated that TBrC not only enhances the protein levels of Bax, cytosolic cytochrome c, caspase-3 and PARP-1 but also reduces the protein expressions of Bcl-2, cyclin D1, VEGFR1 and NF-κB as well as inhibits the phosphorylation and expressions of VEGFR2 and Akt in the cancer cells. More importantly, TBrC displays strong suppression of highly-metastatic tumor growth and reduces the tumor weight by 61.6 % in tumor-bearing mice without toxicity to the mice. Our results suggest that TBrC suppresses the proliferation and migration of lung cancer cells via VEGFR-Akt-NF-κB signaling pathways; TBrC may have a wide therapeutic and/or adjuvant therapeutic application in the treatment of lung cancer.

摘要

为了抑制高度转移性肺癌,这种全球癌症相关死亡的主要原因,开发新的抗癌药物被认为是一种有用且必要的策略。在这项研究中,我们合成了一种新的化合物乙基 6-溴香豆素-3-羧酸-L-茶氨酸(TBrC),并研究了 TBrC 的抗癌活性及其作用机制。我们的结果表明,TBrC 通过诱导细胞凋亡和细胞周期停滞以及调节相关蛋白表达,显著抑制高度转移性肺癌细胞的增殖和迁移。进一步的研究表明,TBrC 不仅增强了 Bax、细胞质细胞色素 c、caspase-3 和 PARP-1 的蛋白水平,还降低了 Bcl-2、cyclin D1、VEGFR1 和 NF-κB 的蛋白表达,并抑制了 VEGFR2 和 Akt 的磷酸化和表达在癌细胞中。更重要的是,TBrC 对荷瘤小鼠没有毒性,却能强烈抑制高度转移性肿瘤的生长,并使肿瘤重量减轻 61.6%。我们的结果表明,TBrC 通过 VEGFR-Akt-NF-κB 信号通路抑制肺癌细胞的增殖和迁移;TBrC 可能在肺癌的治疗或辅助治疗中有广泛的应用前景。

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