Parker Erica N, Song Jiangli, Kishore Kumar G D, Odutola Samuel O, Chavarria Gustavo E, Charlton-Sevcik Amanda K, Strecker Tracy E, Barnes Ashleigh L, Sudhan Dhivya R, Wittenborn Thomas R, Siemann Dietmar W, Horsman Michael R, Chaplin David J, Trawick Mary Lynn, Pinney Kevin G
Department of Chemistry and Biochemistry, Baylor University, One Bear Place #97348, Waco, TX 76798-7348, United States.
Institute of Biomedical Studies, Baylor University, One Bear Place #97224, Waco, TX 76798-7224, United States.
Bioorg Med Chem. 2015 Nov 1;23(21):6974-92. doi: 10.1016/j.bmc.2015.09.036. Epub 2015 Sep 25.
Upregulation of cathepsin L in a variety of tumors and its ability to promote cancer cell invasion and migration through degradation of the extracellular matrix suggest that cathepsin L is a promising biological target for the development of anti-metastatic agents. Based on encouraging results from studies on benzophenone thiosemicarbazone cathepsin inhibitors, a series of fourteen benzoylbenzophenone thiosemicarbazone analogues were designed, synthesized, and evaluated for their inhibitory activity against cathepsins L and B. Thiosemicarbazone inhibitors 3-benzoylbenzophenone thiosemicarbazone 1, 1,3-bis(4-fluorobenzoyl)benzene thiosemicarbazone 8, and 1,3-bis(2-fluorobenzoyl)-5-bromobenzene thiosemicarbazone 32 displayed the greatest potency against cathepsin L with low IC50 values of 9.9 nM, 14.4 nM, and 8.1 nM, respectively. The benzoylbenzophenone thiosemicarbazone analogues evaluated were selective in their inhibition of cathepsin L compared to cathepsin B. Thiosemicarbazone analogue 32 inhibited invasion through Matrigel of MDA-MB-231 breast cancer cells by 70% at 10 μM. Thiosemicarbazone analogue 8 significantly inhibited the invasive potential of PC-3ML prostate cancer cells by 92% at 5 μM. The most active cathepsin L inhibitors from this benzoylbenzophenone thiosemicarbazone series (1, 8, and 32) displayed low cytotoxicity toward normal primary cells [in this case human umbilical vein endothelial cells (HUVECs)]. In an initial in vivo study, 3-benzoylbenzophenone thiosemicarbazone (1) was well-tolerated in a CDF1 mouse model bearing an implanted C3H mammary carcinoma, and showed efficacy in tumor growth delay. Low cytotoxicity, inhibition of cell invasion, and in vivo tolerability are desirable characteristics for anti-metastatic agents functioning through an inhibition of cathepsin L. Active members of this structurally diverse group of benzoylbenzophenone thiosemicarbazone cathepsin L inhibitors show promise as potential anti-metastatic, pre-clinical drug candidates.
组织蛋白酶L在多种肿瘤中上调,并且其通过降解细胞外基质促进癌细胞侵袭和迁移的能力表明,组织蛋白酶L是开发抗转移药物的一个有前景的生物学靶点。基于对二苯甲酮硫代半卡巴腙类组织蛋白酶抑制剂研究的令人鼓舞的结果,设计、合成了一系列14种苯甲酰二苯甲酮硫代半卡巴腙类似物,并评估了它们对组织蛋白酶L和B的抑制活性。硫代半卡巴腙抑制剂3-苯甲酰二苯甲酮硫代半卡巴腙1、1,3-双(4-氟苯甲酰基)苯硫代半卡巴腙8和1,3-双(2-氟苯甲酰基)-5-溴苯硫代半卡巴腙32对组织蛋白酶L表现出最大的效力,IC50值分别低至9.9 nM、14.4 nM和8.1 nM。所评估的苯甲酰二苯甲酮硫代半卡巴腙类似物对组织蛋白酶L的抑制作用相对于组织蛋白酶B具有选择性。硫代半卡巴腙类似物32在10 μM时抑制MDA-MB-231乳腺癌细胞通过基质胶的侵袭达70%。硫代半卡巴腙类似物8在5 μM时显著抑制PC-3ML前列腺癌细胞的侵袭潜能达92%。该苯甲酰二苯甲酮硫代半卡巴腙系列中最具活性的组织蛋白酶L抑制剂(1、8和32)对正常原代细胞[在这种情况下为人脐静脉内皮细胞(HUVECs)]显示出低细胞毒性。在一项初步的体内研究中,3-苯甲酰二苯甲酮硫代半卡巴腙(1)在携带植入的C3H乳腺癌的CDF1小鼠模型中耐受性良好,并在肿瘤生长延迟方面显示出疗效。低细胞毒性、抑制细胞侵袭和体内耐受性是通过抑制组织蛋白酶L发挥作用的抗转移药物所需的特性。这一结构多样的苯甲酰二苯甲酮硫代半卡巴腙类组织蛋白酶L抑制剂中的活性成员有望成为潜在的抗转移临床前候选药物。