Yoon Jung-Ki, Frankel Arthur E, Feun Lynn G, Ekmekcioglu Suhendan, Kim Kevin B
Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA ; Hwasung Public Health Center, Hwasung, South Korea.
Clin Pharmacol. 2013;5:11-9. doi: 10.2147/CPAA.S37350. Epub 2012 Dec 27.
Despite recent development of promising immunotherapeutic and targeted drugs, prognosis in patients with advanced melanoma remains poor, and a cure for this disease remains elusive in most patients. The success of melanoma therapy depends on a better understanding of the biology of melanoma and development of drugs that effectively target the relevant genes or proteins essential for tumor cell survival. Melanoma cells frequently lack argininosuccinate synthetase, an essential enzyme for arginine synthesis, and as a result they become dependent on the availability of exogenous arginine. Accordingly, a therapeutic approach involving depletion of available arginine has been shown to be effective in preclinical studies. Early clinical studies have demonstrated sufficient antitumor activity to give rise to cautious optimism. In this article, the rationale for arginine deprivation therapy is discussed. Additionally, various strategies for depleting arginine are discussed and the preclinical and clinical investigations of arginine deprivation therapy in melanoma are reviewed.
尽管近期有前景的免疫治疗和靶向药物取得了进展,但晚期黑色素瘤患者的预后仍然很差,大多数患者仍难以治愈这种疾病。黑色素瘤治疗的成功取决于对黑色素瘤生物学的更好理解以及开发能够有效靶向肿瘤细胞存活所必需的相关基因或蛋白质的药物。黑色素瘤细胞通常缺乏精氨酸琥珀酸合成酶,这是精氨酸合成的一种必需酶,因此它们变得依赖外源性精氨酸的供应。相应地,一种涉及耗尽可用精氨酸的治疗方法在临床前研究中已被证明是有效的。早期临床研究已证明有足够的抗肿瘤活性,让人产生谨慎的乐观态度。在本文中,将讨论精氨酸剥夺疗法的基本原理。此外,还将讨论耗尽精氨酸的各种策略,并综述黑色素瘤中精氨酸剥夺疗法的临床前和临床研究。