Department of Biotechnology and Bioinformatics, Jaypee University of Information Technology Waknaghat, Solan, 173234, Himachal Pradesh, India.
Cancer Chemother Pharmacol. 2021 Oct;88(4):565-594. doi: 10.1007/s00280-021-04335-w. Epub 2021 Jul 26.
Cancer is the second leading cause of death globally. Chemotherapy and radiation therapy and other medications are employed to treat various types of cancer. However, each treatment has its own set of side effects, owing to its low specificity. As a result, there is an urgent need for newer therapeutics that do not disrupt healthy cells' normal functioning. Depriving nutrient or non/semi-essential amino acids to which cancerous cells are auxotrophic remains one such promising anticancer strategy. L-Arginine (Arg) is a semi-essential vital amino acid involved in versatile metabolic processes, signaling pathways, and cancer cell proliferation. Hence, the administration of Arg depriving enzymes (ADE) such as arginase, arginine decarboxylase (ADC), and arginine deiminase (ADI) could be effective in cancer therapy. The Arg auxotrophic cancerous cells like hepatocellular carcinoma, human colon cancer, leukemia, and breast cancer cells are sensitive to ADE treatment due to low expression of crucial enzymes argininosuccinate synthetase (ASS), argininosuccinate lyase (ASL), and ornithine transcarbamylase (OCT). These therapeutic enzyme treatments induce cell death through inducing autophagy, apoptosis, generation of oxidative species, i.e., oxidative stress, and arresting the progression and expansion of cancerous cells at certain cell cycle checkpoints. The enzymes are undergoing clinical trials and could be successfully exploited as potential anticancer agents in the future.
癌症是全球第二大致死原因。化疗、放疗和其他药物被用于治疗各种类型的癌症。然而,每种治疗方法都有其自身的副作用,因为其特异性低。因此,迫切需要新的治疗方法,这些方法不会干扰健康细胞的正常功能。剥夺癌症细胞依赖的营养物质或非/半必需氨基酸仍然是一种有前途的抗癌策略。L-精氨酸(Arg)是一种半必需的重要氨基酸,参与多种代谢过程、信号通路和癌细胞增殖。因此,施用 Arg 剥夺酶(ADE),如精氨酸酶、精氨酸脱羧酶(ADC)和精氨酸脱氨酶(ADI),可能对癌症治疗有效。Arg 营养缺陷型癌细胞,如肝癌、人结肠癌、白血病和乳腺癌细胞,由于关键酶精氨酸合成酶(ASS)、精氨酸琥珀酸裂解酶(ASL)和鸟氨酸氨甲酰转移酶(OCT)表达水平低,对 ADE 治疗敏感。这些治疗性酶通过诱导自噬、细胞凋亡、产生氧化物质(即氧化应激)和阻止癌细胞在特定细胞周期检查点的进展和扩张,诱导细胞死亡。这些酶正在进行临床试验,将来可能会成功地被开发为潜在的抗癌药物。