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精氨酸剥夺疗法的潜力解锁:癌症治疗的最新突破和广阔前景。

Unlocking the Potential of Arginine Deprivation Therapy: Recent Breakthroughs and Promising Future for Cancer Treatment.

机构信息

Liver Research Center, Chang Gung Memorial Hospital, Linkou Branch, Taoyuan 333, Taiwan.

Department of Pediatrics, Chang Gung Memorial Hospital, Linkou Branch and Chang Gung University College of Medicine, Taoyuan 333, Taiwan.

出版信息

Int J Mol Sci. 2023 Jun 26;24(13):10668. doi: 10.3390/ijms241310668.

Abstract

Arginine is a semi-essential amino acid that supports protein synthesis to maintain cellular functions. Recent studies suggest that arginine also promotes wound healing, cell division, ammonia metabolism, immune system regulation, and hormone biosynthesis-all of which are critical for tumor growth. These discoveries, coupled with the understanding of cancer cell metabolic reprogramming, have led to renewed interest in arginine deprivation as a new anticancer therapy. Several arginine deprivation strategies have been developed and entered clinical trials. The main principle behind these therapies is that arginine auxotrophic tumors rely on external arginine sources for growth because they carry reduced key arginine-synthesizing enzymes such as argininosuccinate synthase 1 (ASS1) in the intracellular arginine cycle. To obtain anticancer effects, modified arginine-degrading enzymes, such as PEGylated recombinant human arginase 1 (rhArg1-PEG) and arginine deiminase (ADI-PEG 20), have been developed and shown to be safe and effective in clinical trials. They have been tried as a monotherapy or in combination with other existing therapies. This review discusses recent advances in arginine deprivation therapy, including the molecular basis of extracellular arginine degradation leading to tumor cell death, and how this approach could be a valuable addition to the current anticancer arsenal.

摘要

精氨酸是一种半必需氨基酸,可支持蛋白质合成以维持细胞功能。最近的研究表明,精氨酸还能促进伤口愈合、细胞分裂、氨代谢、免疫系统调节和激素生物合成——所有这些都是肿瘤生长所必需的。这些发现,加上对癌细胞代谢重编程的理解,重新引发了人们对精氨酸剥夺作为一种新的抗癌疗法的兴趣。已经开发了几种精氨酸剥夺策略并进入临床试验。这些疗法的主要原理是,精氨酸营养缺陷型肿瘤依赖外部精氨酸来源来生长,因为它们在细胞内精氨酸循环中携带减少的关键精氨酸合成酶,如精氨琥珀酸合成酶 1(ASS1)。为了获得抗癌效果,已经开发了修饰的精氨酸降解酶,如聚乙二醇化重组人精氨酸酶 1(rhArg1-PEG)和精氨酸脱氨酶(ADI-PEG 20),并在临床试验中证明是安全有效的。它们已被尝试作为单一疗法或与其他现有疗法联合使用。本文综述了精氨酸剥夺疗法的最新进展,包括导致肿瘤细胞死亡的细胞外精氨酸降解的分子基础,以及这种方法如何成为当前抗癌武器库的有价值的补充。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec50/10341449/cb4211f38411/ijms-24-10668-g001.jpg

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