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Anti-angiogenic effects of trabectedin (Yondelis; ET-743) on human breast cancer cells

机译:曲贝汀(Yondelis; ET-743)对人乳腺癌细胞的抗血管生成作用

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摘要

Trabectedin, a tetrahydroisoquinoline alkaloid derived from a Caribbean tunicate Ecteinascidia turbinata, has been shown to have antitumor effects. In this study, we assessed the possible anti-angiogenic effects of trabectedin on human umbilical vein endothelial cells (HUVECs) and breast cancer cell lines. An XTT cell viability assay was used to determine cytotoxicity. A scratch assay was used to detect the migration of cells after trabectedin treatment. Angiogenic cytokine profiles of breast cancer cell lines, before and after treatment with trabectedin, were investigated using an angiogenesis antibody array. Changes in mRNA expression levels of VEGF were evaluated using qRT-PCR. Trabectedin inhibited the viability of HUVECs and breast cancer cells in a concentration-and time-dependent manner. The migration of both HUVECs and breast cancer cells was suppressed by trabectedin treatment. Angiogenic cytokines which are known to regulate tumorigenicity and angiogenesis, such as GM-CSF, IGFBP-2, VEGF, and uPA, were inhibited, while several anti-angiogenic cytokines such as TIMP-1 and Serpin E1were induced in breast cancer cells. Furthermore, expression levels of VEGF mRNA were inhibited in all breast cancer cells tested. Although additional studies are needed to elucidate the molecular mechanisms underlying the anti-angiogenic activity of trabectedin, our results suggest that trabectedin may act as a potential anti-angiogenic agent in breast cancer cells.
机译:Trabectedin是一种四氢异喹啉类生物碱,其衍生自加勒比海被膜钩端螺旋藻(Ecteinascidia turbinata),具有抗肿瘤作用。在这项研究中,我们评估了曲贝汀对人脐静脉内皮细胞(HUVEC)和乳腺癌细胞系的可能抗血管生成作用。 XTT细胞生存力测定法用于确定细胞毒性。 trabectedin处理后,使用刮擦试验检测细胞的迁移。使用血管生成抗体阵列研究了曲贝汀治疗前后的乳腺癌细胞系的血管生成细胞因子谱。使用qRT-PCR评估VEGF的mRNA表达水平的变化。 Trabectedin以浓度和时间依赖性方式抑制HUVEC和乳腺癌细胞的活力。曲贝汀治疗可抑制HUVEC和乳腺癌细胞的迁移。已知可以调节致癌性和血管生成的血管生成细胞因子,例如GM-CSF,IGFBP-2,VEGF和uPA,而在乳腺癌细胞中可以诱导出几种抗血管生成细胞因子,例如TIMP-1和Serpin E1。此外,在所有测试的乳腺癌细胞中VEGF mRNA的表达水平均被抑制。尽管需要更多的研究来阐明trabectedin的抗血管生成活性的分子机制,但我们的结果表明trabectedin可能在乳腺癌细胞中充当潜在的抗血管生成剂。

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