Fultang Livingstone, Vardon Ashley, De Santo Carmela, Mussai Francis
Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.
Int J Cancer. 2016 Aug 1;139(3):501-9. doi: 10.1002/ijc.30051. Epub 2016 Apr 15.
Renewed interest in the use of therapeutic enzymes combined with an improved knowledge of cancer cell metabolism, has led to the translation of several arginine depletion strategies into early phase clinical trials. Arginine auxotrophic tumors are reliant on extracellular arginine, due to the downregulation of arginosuccinate synthetase or ornithine transcarbamylase-key enzymes for intracellular arginine recycling. Engineered arginine catabolic enzymes such as recombinant human arginase (rh-Arg1-PEG) and arginine deiminase (ADI-PEG) have demonstrated cytotoxicity against arginine auxotrophic tumors. In this review, we discuss the molecular events triggered by extracellular arginine depletion that contribute to tumor cell death.
对治疗性酶使用的重新关注,再加上对癌细胞代谢认识的提高,已促使几种精氨酸消耗策略进入早期临床试验阶段。精氨酸营养缺陷型肿瘤依赖细胞外精氨酸,这是由于精氨琥珀酸合成酶或鸟氨酸转氨甲酰酶(细胞内精氨酸循环的关键酶)下调所致。工程化的精氨酸分解酶,如重组人精氨酸酶(rh-Arg1-PEG)和精氨酸脱亚氨酶(ADI-PEG),已显示出对精氨酸营养缺陷型肿瘤的细胞毒性。在本综述中,我们讨论了细胞外精氨酸消耗引发的导致肿瘤细胞死亡的分子事件。