Department of Biochemistry, Molecular Biology & Biophysics, University of Minnesota, Minneapolis, MN, 55455, USA.
Invest New Drugs. 2013 Oct;31(5):1142-50. doi: 10.1007/s10637-013-9932-0. Epub 2013 Feb 8.
Previously, we reported on the anti-tumor activities of two designed calix[4]arene-based topomimetics (PTX008 and PTX009) of the amphipathic, angiostatic peptide Anginex. Here, we chemically modified the hydrophobic and hydrophilic faces of PTX008 and PTX009, and discovered new calixarene compounds that are more potent, cytotoxic anti-tumor agents. One of them, PTX013, is particularly effective at inhibiting the growth of several human cancer cell lines, as well as drug resistant cancer cells. Mechanistically, PTX013 induces cell cycle arrest in sub-G1 and G0/G1 phases of e.g. SQ20B cells, a radio-resistant human head and neck carcinoma model. In the syngeneic B16F10 melanoma tumor mouse model, PTX013 (0.5 mg/Kg) inhibits tumor growth by about 50-fold better than parent PTX008. A preliminary pharmacodynamics study strongly suggests that PTX013 exhibits good in vivo exposure and a relatively long half-life. Overall, this research contributes to the discovery of novel therapeutics as potentially useful agents against cancer in the clinic.
此前,我们曾报道过两种基于杯[4]芳烃的拟 Topo 结构的抗肿瘤活性(PTX008 和 PTX009),它们是两亲性血管生成抑制肽 Anginex 的类似物。在此,我们对 PTX008 和 PTX009 的疏水面和亲水面进行了化学修饰,发现了新的杯芳烃化合物,它们具有更强的细胞毒性抗肿瘤活性。其中一种化合物 PTX013 特别有效地抑制了几种人癌细胞系以及耐药癌细胞的生长。从机制上讲,PTX013 诱导例如 SQ20B 细胞的细胞周期停滞在亚 G1 和 G0/G1 期。在同种 B16F10 黑素瘤肿瘤小鼠模型中,PTX013(0.5mg/Kg)的肿瘤生长抑制作用比亲本化合物 PTX008 强约 50 倍。初步的药效学研究强烈表明,PTX013 具有良好的体内暴露和相对较长的半衰期。总的来说,这项研究有助于发现新的治疗方法,为临床癌症治疗提供潜在有用的药物。