Entremed Inc., 101 College Street, Toronto, Ontario, Canada M5G 1L7.
Mol Cancer Ther. 2011 Jan;10(1):126-37. doi: 10.1158/1535-7163.MCT-10-0574. Epub 2010 Dec 21.
ENMD-2076 is a novel orally active, small molecule kinase inhibitor with a mechanism of action involving several pathways key to tumor growth and survival: angiogenesis, proliferation, and the cell cycle. ENMD-2076 has selective activity against the mitotic kinase Aurora A, as well as kinases involved in angiogenesis (VEGFRs, FGFRs). ENMD-2076 inhibited the growth in vitro of a wide range of human solid tumor and hematopoietic cancer cell lines with IC(50) values ranging from 0.025 to 0.7 μmol/L. ENMD-2076 was also shown to induce regression or complete inhibition of tumor growth in vivo at well-tolerated doses in tumor xenograft models derived from breast, colon, melanoma, leukemia, and multiple myeloma cell lines. Pharmacodynamic experiments in vivo showed that in addition to inhibiting Aurora A, single doses of ENMD-2076 had sustained inhibitory effects on the activation of Flt3 as well as the angiogenic tyrosine kinases, VEGFR2/KDR and FGFR1 and 2. ENMD-2076 was shown to prevent the formation of new blood vessels and regress formed vessels in vivo at doses equivalent to those that gave substantial activity in tumor xenograft models. These results indicate that ENMD-2076 is a well-tolerated, orally active multitarget kinase inhibitor with a unique antiangiogenic/antiproliferative profile and provides strong preclinical support for use as a therapeutic for human cancers. Several phase 1 studies involving ENMD-2076 have been recently completed, and the compound is currently being evaluated in a phase 2 clinical trial in patients with platinum-resistant ovarian cancer.
ENMD-2076 是一种新型的、口服活性的小分子激酶抑制剂,其作用机制涉及到肿瘤生长和存活的几个关键途径:血管生成、增殖和细胞周期。ENMD-2076 对有丝分裂激酶 Aurora A 以及参与血管生成的激酶(VEGFRs、FGFRs)具有选择性活性。ENMD-2076 抑制了广泛的人类实体瘤和造血癌细胞系的体外生长,IC50 值范围为 0.025 至 0.7 μmol/L。在源于乳腺癌、结肠癌、黑色素瘤、白血病和多发性骨髓瘤细胞系的肿瘤异种移植模型中,以耐受良好的剂量给予 ENMD-2076 也显示出诱导肿瘤消退或完全抑制肿瘤生长的作用。体内药效学实验表明,除了抑制 Aurora A 之外,ENMD-2076 的单次剂量还对 Flt3 的激活以及血管生成酪氨酸激酶 VEGFR2/KDR 和 FGFR1 和 2 具有持续的抑制作用。ENMD-2076 被证明可以预防新血管的形成并使体内已形成的血管退化,其剂量相当于在肿瘤异种移植模型中具有显著活性的剂量。这些结果表明,ENMD-2076 是一种耐受性良好的、口服活性的多靶点激酶抑制剂,具有独特的抗血管生成/抗增殖特征,并为将其用作人类癌症的治疗药物提供了强有力的临床前支持。最近完成了几项涉及 ENMD-2076 的 1 期研究,该化合物目前正在铂耐药卵巢癌患者中进行 2 期临床试验评估。