Brown P D
British Biotech Pharmaceuticals Ltd, Oxford, U.K.
Adv Enzyme Regul. 1995;35:293-301. doi: 10.1016/0065-2571(94)00022-u.
Matrix metalloproteinase inhibitors represent a new therapeutic approach to the treatment of advanced cancer. These inhibitors block the activity of proteolytic enzymes, matrix metalloproteinases, used by tumor cells to break down and remodel tissue matrices during the process of metastatic spread. As such they were regarded initially as inhibitors of metastasis. However, recent studies have shown that these inhibitors can also act to inhibit tumor growth by (i) preventing local invasion and promoting stromal encapsulation and (ii) by inhibiting tumor neovascularization. Matrix metalloproteinase inhibitors therefore have the potential to halt tumor progression and it is possible to envision their use as a low toxicity complement to cytotoxic therapies. Batimastat (BB-94) is the first inhibitor of this class to enter clinical trial in cancer patients. In a phase I/II trial in patients with malignant ascites batimastat was well tolerated and there were preliminary signs of efficacy.
基质金属蛋白酶抑制剂代表了一种治疗晚期癌症的新方法。这些抑制剂可阻断蛋白水解酶即基质金属蛋白酶的活性,肿瘤细胞在转移扩散过程中利用这些酶来分解和重塑组织基质。因此,它们最初被视为转移抑制剂。然而,最近的研究表明,这些抑制剂还可通过以下方式抑制肿瘤生长:(i)防止局部侵袭并促进基质包裹;(ii)抑制肿瘤新生血管形成。因此,基质金属蛋白酶抑制剂有可能阻止肿瘤进展,并且可以设想将其用作细胞毒性疗法的低毒性补充剂。batimastat(BB - 94)是此类抑制剂中首个进入癌症患者临床试验的药物。在一项针对恶性腹水患者的I/II期试验中,batimastat耐受性良好,并有初步疗效迹象。