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首页> 外文期刊>Cancers >Molecular Mechanisms Underlying Yatein-Induced Cell-Cycle Arrest and Microtubule Destabilization in Human Lung Adenocarcinoma Cells
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Molecular Mechanisms Underlying Yatein-Induced Cell-Cycle Arrest and Microtubule Destabilization in Human Lung Adenocarcinoma Cells

机译:亚森诱导的细胞周期停滞和人肺腺癌细胞中微管稳定化的分子机制

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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 G 2 /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:Yatein是从Calocedrus Formosana Florin提取物中分离的抗肿瘤剂。在我们以前的研究中,我们发现Yatein通过诱导内在和外在凋亡途径来抑制人肺腺癌A549和Cl1-5细胞的生长。为了进一步揭示亚丹素诱导抑制对A549和Cl1-5细胞生长的影响和机制,我们评估了亚丹林介导的体内抗肿瘤活性和亚丹林对细胞周期进展和微管动力学的调节作用。流式细胞术和Western印迹显示Yatein在A549和Cl1-5细胞中诱导G 2 / M停滞。 Yatein也破坏了微管和干扰两条细胞系中的微管动态。此外,我们评估了使用异种移植小鼠模型在体内体内的抗肿瘤活性,发现Yatein治疗改变了细胞周期蛋白B / CDC2复杂表达,并显着抑制肿瘤生长。我们的结果表明,亚丹林有效地抑制了A549和Cl1-5细胞的生长,可能是扰乱细胞周期进展和微管动态。

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