Victor Bernadette C, Sloane Bonnie F
Department of Pharmacology and Barbara Ann Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Biol Chem. 2007 Nov;388(11):1131-40. doi: 10.1515/BC.2007.150.
Cysteine cathepsins play a fundamental role in tumor growth, invasion and migration, angiogenesis, and the metastatic cascade. Evidence of their overexpression in a wide array of human tumors has been well documented. Cysteine cathepsins seem to have a characteristic location-function relationship that leads to non-traditional roles such as those in development and pathology. For example, during tumor development, some cysteine cathepsins are found not just within lysosomes, but are also redistributed into presumptive exocytic vesicles at the cell periphery, resulting in their secretion. This altered localization contributes to non-lysosomal functions that have been linked to malignant progression. Mechanisms for altered localization are not well understood, but do include the interaction of cysteine cathepsins with binding partners that modulate intracellular trafficking and association with specific regions on the cell surface.
半胱氨酸组织蛋白酶在肿瘤生长、侵袭与迁移、血管生成以及转移级联反应中发挥着重要作用。它们在多种人类肿瘤中过度表达的证据已有充分记录。半胱氨酸组织蛋白酶似乎具有独特的定位 - 功能关系,这导致了其在发育和病理学等非传统领域的作用。例如,在肿瘤发展过程中,一些半胱氨酸组织蛋白酶不仅存在于溶酶体内,还会重新分布到细胞周边的假定胞吐小泡中,从而导致其分泌。这种定位改变促成了与恶性进展相关的非溶酶体功能。定位改变的机制尚不完全清楚,但确实包括半胱氨酸组织蛋白酶与调节细胞内运输以及与细胞表面特定区域结合的结合伴侣之间的相互作用。