Tang Ke, Luo Can, Li Yan, Lu Chenshu, Zhou Wanqi, Huang Haihong, Chen Xiaoguang
State Key Laboratory of Bioactive Substances and Functions of Nature Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
PLoS One. 2014 Jul 8;9(7):e101889. doi: 10.1371/journal.pone.0101889. eCollection 2014.
In this study, our objective is to evaluate the potential of a novel Sorafenib derivative, named HLC-080, as a new anticancer agent for colon cancer. We firstly carried out MTT assay, colony formation assay, flow cytometry analysis and transwell invasion assay to determine effect of our compound HLC-080 on cell viability, anti-proliferation activity, cell cycle arrest and the intervention on cell invasion, respectively. On the other hand, in vivo antitumor activity of HLC-080 was also tested using H22 xenograft model and the angiogenesis effect of HLC-080 was measured by EA.hy926 tube formation assay. The expression levels of various proteins in HLC-080 treated with HT-29 cell lines were examined using Western blot and ELISA experiments. The results showed that HLC-080 could dramatically inhibit the growth and colony formation of various tumor cells, therefore exhibited remarkable antitumor activity. HLC-080 can induce cell cycle arrest at G1 phase in HT-29 cells and subsequently inhibit the invasive potential of colon cancer cells. HLC-080 also exhibits anti-angiogenesis effect in EA.hy926 model. Additionally, the in vivo study showed that HLC-080 was able to reduced the tumor weight with the rate of 35.81%. And at the concentration of 0.352±0.034 µM, HLC-080 is able to reduce half of the regular protein level of p-c-Raf (Ser259), consequently block Raf/MEK/ERK signaling in HT-29 cell lines. In conclusion, our study suggests that Sorafenib derivative HLC-080 has the potential to inhibit cell proliferation and angiogenesis, Since, HLC-080 is particularly active against human colon cancer cells, our study highlights that HLC-080 and its related analogues may serve as a new anti-cancer drug, particularly against colon cancer.
在本研究中,我们的目标是评估一种名为HLC-080的新型索拉非尼衍生物作为结肠癌新抗癌药物的潜力。我们首先进行了MTT试验、集落形成试验、流式细胞术分析和Transwell侵袭试验,以分别确定我们的化合物HLC-080对细胞活力、抗增殖活性、细胞周期阻滞和细胞侵袭干预的影响。另一方面,还使用H22异种移植模型测试了HLC-080的体内抗肿瘤活性,并通过EA.hy926管形成试验测量了HLC-080的血管生成作用。使用蛋白质印迹和ELISA实验检测了用HT-29细胞系处理的HLC-080中各种蛋白质的表达水平。结果表明,HLC-080可显著抑制各种肿瘤细胞的生长和集落形成,因此表现出显著的抗肿瘤活性。HLC-080可诱导HT-29细胞的细胞周期阻滞在G1期,随后抑制结肠癌细胞的侵袭潜能。HLC-080在EA.hy926模型中也表现出抗血管生成作用。此外,体内研究表明,HLC-080能够使肿瘤重量降低35.81%。在浓度为0.352±0.034µM时,HLC-080能够将p-c-Raf(Ser259)的正常蛋白水平降低一半,从而阻断HT-29细胞系中的Raf/MEK/ERK信号传导。总之,我们的研究表明索拉非尼衍生物HLC-080具有抑制细胞增殖和血管生成的潜力,由于HLC-080对人结肠癌细胞特别有效,我们的研究强调HLC-080及其相关类似物可能作为一种新的抗癌药物,特别是针对结肠癌。