Mannello Ferdinando
Istituto di Istologia ed Analisi di Laboratorio, Università Studi "Carlo Bo", Urbino, Italy.
Recent Pat Anticancer Drug Discov. 2006 Jan;1(1):91-103. doi: 10.2174/157489206775246421.
The matrix metalloproteinases (MMPs), belonging to the family of proteolytic enzymes, are well-known for their ability to degrade the extracellular matrix, and are involved in many aspects of both physiological cellular processes and pathological situations, such as tumor growth, invasion and metastasis. MMPs have been considered prognostic factors in various types of cancer as well as promising targets for cancer therapy. Although preclinical studies of a number of different synthetic MMP inhibitors have been identified as cytostatic and anti-angiogenic agents and have begun clinical testing, the past years have produced a consistent number of disappointments and limited successes. In view of their specific implication in malignant tissues, several natural compounds were utilized, and the results were so satisfactory as to encourage several clinical trials in order to improve efficacy and to reduce the side effect profile. The natural protection against cancer has been receiving a great deal of attention, and the critical examination of previous studies shed light on new information about the source and function of MMPs, focusing the attention on the identification of MMP targets in tumors. This review discusses the current knowledge and research in the field of natural MMP inhibitor as innovative therapeutic intervention in cancer.
基质金属蛋白酶(MMPs)属于蛋白水解酶家族,以其降解细胞外基质的能力而闻名,并参与生理细胞过程和病理情况的许多方面,如肿瘤生长、侵袭和转移。MMPs被认为是各类癌症的预后因素以及癌症治疗的有前景的靶点。尽管许多不同的合成MMP抑制剂的临床前研究已被确定为细胞生长抑制剂和抗血管生成剂,并已开始临床试验,但过去几年却产生了一系列的失望结果和有限的成功。鉴于它们在恶性组织中的特定作用,人们使用了几种天然化合物,结果非常令人满意,从而鼓励了几项临床试验,以提高疗效并降低副作用。天然抗癌保护作用一直备受关注,对以往研究的批判性审视揭示了有关MMPs来源和功能的新信息,将注意力集中在肿瘤中MMP靶点的识别上。本综述讨论了天然MMP抑制剂领域的当前知识和研究,作为癌症的创新治疗干预手段。