Lebreton Sylvain, Jaunbergs Janis, Roth Michael G, Ferguson Deborah A, De Brabander Jef K
Department of Biochemistry, University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Blvd., Dallas, TX 75390-9038, USA.
Bioorg Med Chem Lett. 2008 Nov 15;18(22):5879-83. doi: 10.1016/j.bmcl.2008.07.003. Epub 2008 Jul 5.
The natural product salicylihalamide is a potent inhibitor of the Vacuolar ATPase (V-ATPase), a potential target for antitumor chemotherapy. We generated salicylihalamide-resistant tumor cell lines typified by an overexpansion of lysosomal organelles. We also found that many tumor cell lines upregulate tissue-specific plasmalemmal V-ATPases, and hypothesize that tumors that derive their energy from glycolysis rely on these isoforms to maintain a neutral cytosolic pH. To further validate the potential of V-ATPase inhibitors as leads for cancer chemotherapy, we developed a multigram synthesis of the potent salicylihalamide analog saliphenylhalamide.
天然产物水杨酰卤酰胺是液泡型ATP酶(V-ATP酶)的强效抑制剂,而V-ATP酶是抗肿瘤化疗的一个潜在靶点。我们构建了以溶酶体细胞器过度扩张为特征的水杨酰卤酰胺耐药肿瘤细胞系。我们还发现许多肿瘤细胞系上调组织特异性质膜V-ATP酶,并推测通过糖酵解获取能量的肿瘤依赖这些同工型来维持胞质pH值中性。为了进一步验证V-ATP酶抑制剂作为癌症化疗先导物的潜力,我们开发了多克规模合成强效水杨酰卤酰胺类似物水杨酰苯卤酰胺的方法。