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代谢抗肿瘤治疗中的酶。

Enzymes in Metabolic Anticancer Therapy.

机构信息

Department of Molecular Medicine, Unit of Immunology and General Pathology, University of Pavia, Pavia, Italy.

出版信息

Adv Exp Med Biol. 2019;1148:173-199. doi: 10.1007/978-981-13-7709-9_9.

Abstract

Cancer treatment has greatly improved over the last 50 years, but it remains challenging in several cases. Useful therapeutic targets are normally unique peculiarities of cancer cells that distinguish them from normal cells and that can be tackled with appropriate drugs. It is now known that cell metabolism is rewired during tumorigenesis and metastasis as a consequence of oncogene activation and oncosuppressors inactivation, leading to a new cellular homeostasis typically directed towards anabolism. Because of these modifications, cells can become strongly or absolutely dependent on specific substrates, like sugars, lipids or amino acids. Cancer addictions are a relevant target for therapy, as removal of an essential substrate can lead to their selective cell-cycle arrest or even to cell death, leaving normal cells untouched. Enzymes can act as powerful agents in this respect, as demonstrated by asparaginase, which has been included in the treatment of Acute Lymphoblastic Leukemia for half a century. In this review, a short outline of cancer addictions will be provided, focusing on the main cancer amino acid dependencies described so far. Therapeutic enzymes which have been already experimented at the clinical level will be discussed, along with novel potential candidates that we propose as new promising molecules. The intrinsic limitations of their present molecular forms, along with molecular engineering solutions to explore, will also be presented.

摘要

在过去的 50 年里,癌症治疗有了很大的改善,但在某些情况下仍然具有挑战性。有用的治疗靶点通常是癌细胞特有的独特特征,它们可以与适当的药物结合使用。现在已知,肿瘤发生和转移过程中,细胞代谢会因癌基因激活和抑癌基因失活而重新布线,导致新的细胞内稳态通常朝向合成代谢。由于这些变化,细胞可能会强烈或绝对依赖于特定的底物,如糖、脂质或氨基酸。癌症成瘾是治疗的一个重要靶点,因为去除必需的底物会导致它们的细胞周期选择性停滞甚至细胞死亡,而正常细胞不受影响。酶在这方面可以发挥强大的作用,天冬酰胺酶就是一个很好的例子,它已经被纳入急性淋巴细胞白血病的治疗中长达半个世纪。在这篇综述中,将提供癌症成瘾的简要概述,重点介绍迄今为止描述的主要癌症氨基酸依赖性。将讨论已经在临床水平上进行试验的治疗性酶,以及我们提出的作为新的有前途的分子的新型潜在候选物。还将介绍它们目前分子形式的固有局限性,以及探索所需的分子工程解决方案。

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