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Molecular Mechanisms Underlying Yatein-Induced Cell-Cycle Arrest and Microtubule Destabilization in Human Lung Adenocarcinoma Cells

机译:叶酸诱导人肺腺癌细胞的细胞周期阻滞和微管失稳的分子机制。

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摘要

Yatein is an antitumor agent isolated from Calocedrus formosana Florin leaves extract. In our previous study, we found that yatein inhibited the growth of human lung adenocarcinoma A549 and CL1-5 cells by inducing intrinsic and extrinsic apoptotic pathways. To further uncover the effects and mechanisms of yatein-induced inhibition on A549 and CL1-5 cell growth, we evaluated yatein-mediated antitumor activity in vivo and the regulatory effects of yatein on cell-cycle progression and microtubule dynamics. Flow cytometry and western blotting revealed that yatein induces G2/M arrest in A549 and CL1-5 cells. Yatein also destabilized microtubules and interfered with microtubule dynamics in the two cell lines. Furthermore, we evaluated the antitumor activity of yatein in vivo using a xenograft mouse model and found that yatein treatment altered cyclin B/Cdc2 complex expression and significantly inhibited tumor growth. Taken together, our results suggested that yatein effectively inhibited the growth of A549 and CL1-5 cells possibly by disrupting cell-cycle progression and microtubule dynamics.
机译:叶黄素是一种从中华绒螯蟹弗洛林叶提取物中分离出来的抗肿瘤剂。在我们以前的研究中,我们发现叶黄素通过诱导内在和外在的凋亡途径来抑制人肺腺癌A549和CL1​​-5细胞的生长。为了进一步揭示叶黄素诱导的抑制作用对A549和CL1​​-5细胞生长的影响和机制,我们评估了叶黄素介导的体内抗肿瘤活性以及叶黄素对细胞周期进程和微管动力学的调节作用。流式细胞仪和western blotting显示叶黄素诱导A549和CL1​​-5细胞中的G2 / M阻滞。叶黄素还破坏了微管的稳定性,并干扰了两种细胞系中的微管动力学。此外,我们使用异种移植小鼠模型评估叶黄素在体内的抗肿瘤活性,并发现叶黄素治疗改变了细胞周期蛋白B / Cdc2复合物的表达并显着抑制了肿瘤的生长。综上所述,我们的结果表明叶黄素可能通过破坏细胞周期进程和微管动力学来有效抑制A549和CL1​​-5细胞的生长。

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