McAtee Caitlin O, Barycki Joseph J, Simpson Melanie A
Department of Biochemistry, University of Nebraska, Lincoln, Nebraska, USA.
Department of Biochemistry, University of Nebraska, Lincoln, Nebraska, USA.
Adv Cancer Res. 2014;123:1-34. doi: 10.1016/B978-0-12-800092-2.00001-0.
Hyaluronidases are a family of five human enzymes that have been differentially implicated in the progression of many solid tumor types, both clinically and in functional studies. Advances in the past 5 years have clarified many apparent contradictions: (1) by demonstrating that specific hyaluronidases have alternative substrates to hyaluronan (HA) or do not exhibit any enzymatic activity, (2) that high-molecular weight HA polymers elicit signaling effects that are opposite those of the hyaluronidase-digested HA oligomers, and (3) that it is actually the combined overexpression of HA synthesizing enzymes with hyaluronidases that confers tumorigenic potential. This review examines the literature supporting these conclusions and discusses novel mechanisms by which hyaluronidases impact invasive tumor cell processes. In addition, a detailed structural and functional comparison of the hyaluronidases is presented with insights into substrate selectivity and potential for therapeutic targeting. Finally, technological advances in targeting hyaluronidase for tumor imaging and cancer therapy are summarized.
透明质酸酶是一个由五种人类酶组成的家族,在许多实体瘤类型的进展过程中,无论是在临床研究还是功能研究中,都有着不同程度的牵连。过去五年的研究进展澄清了许多明显的矛盾之处:(1)通过证明特定的透明质酸酶具有除透明质酸(HA)之外的其他底物,或者不表现出任何酶活性;(2)高分子量HA聚合物引发的信号效应与透明质酸酶消化后的HA寡聚体相反;(3)实际上是HA合成酶与透明质酸酶的联合过度表达赋予了肿瘤发生潜能。本综述考察了支持这些结论的文献,并讨论了透明质酸酶影响侵袭性肿瘤细胞进程的新机制。此外,还对透明质酸酶进行了详细的结构和功能比较,深入探讨了底物选择性和治疗靶向潜力。最后,总结了针对透明质酸酶进行肿瘤成像和癌症治疗的技术进展。