唐克, 杨瀚泽, 李燕, 田康, 李超, 周琬琪, 牛非, 冯志强, 陈晓光. 小分子靶向化合物T03的抗肿瘤作用及机制研究J. 药学学报, 2014,49(6): 861-868.
引用本文: 唐克, 杨瀚泽, 李燕, 田康, 李超, 周琬琪, 牛非, 冯志强, 陈晓光. 小分子靶向化合物T03的抗肿瘤作用及机制研究J. 药学学报, 2014,49(6): 861-868.
TANG Ke, YANG Han-ze, LI Yan, TIAN Kang, LI Chao, ZHOU Wan-qi, NIU Fei, FENG Zhi-qiang, CHEN Xiao-guang. Anti-tumor activity and mechanism of T03 in vitro and in vivoJ. Acta Pharmaceutica Sinica, 2014,49(6): 861-868.
Citation: TANG Ke, YANG Han-ze, LI Yan, TIAN Kang, LI Chao, ZHOU Wan-qi, NIU Fei, FENG Zhi-qiang, CHEN Xiao-guang. Anti-tumor activity and mechanism of T03 in vitro and in vivoJ. Acta Pharmaceutica Sinica, 2014,49(6): 861-868.

小分子靶向化合物T03的抗肿瘤作用及机制研究

Anti-tumor activity and mechanism of T03 in vitro and in vivo

  • 摘要: 研究T03在体内、外的抗肿瘤作用,并对其作用机制进行初步探讨。采用MTT和集落形成实验检测T03体外抗肿瘤活性,小鼠移植瘤模型观察T03的体内抗肿瘤作用。FCM实验观察其对肿瘤细胞凋亡及细胞周期的影响,Western blotting检测初步探讨该化合物的作用机制。结果显示,T03对肝癌及肾癌细胞具有较好的抑 制增殖活性,可明显抑制肝癌细胞的集落形成,促进肝癌细胞凋亡,改变细胞周期。T03(0.16 mmol·kg-1)可抑 制小鼠肾癌移植瘤Renca的生长,抑瘤率可达42.30%。Western blotting结果显示,T03的抗肿瘤作用与抑制AKT/mTOR、Raf/MEK/ERK信号通路以及促进细胞凋亡蛋白表达有关。T03在体内外均具有一定的抗肿瘤作用。

     

    Abstract: The purpose of this study is to investigate the activity and mechanism of a new anti-tumor agent T03.MTT and colony formation assay were performed to determine anti-proliferation activity of T03 in vitro.Antitumor activity was observed by Renca xenograft model in vivo.The effect of T03 on cell cycle and apoptosis were measured by FCM analysis.Western blotting was performed to investigate the expression level of proteins in HepG2 cell lines treated with T03.T03 had anti-tumor activity by inhibiting tumor cell growth and colony formation in vitro, especially on hepatocellular carcinoma cells (HCC).At the concentration of 10 μmol·L-1, T03 induced cell apoptosis and cell cycle arrest in HCC.Moreover, it proved that T03 reducedthe tumor weight with the rate of 42.30% without any obviously side effect in Renca xenograft model.At the concentration of 2.0 μmol·L-1, T03 was able to reduce the level of p-c-Raf (Ser259), and thus blocked Raf/MEK/ERK and AKT signaling in HepG2 cell lines.The result suggested that T03 has the potential to inhibit cell proliferation and induce cell apoptosis both in vitro and in vivo, particularly active against HCC, indicating T03 and its analogues may serve as a new anti-cancer drug against hepatocellular carcinoma.

     

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