l-Asparaginase Bio-Betters: Insight Into Current Formulations, Optimization Strategies and Future Bioengineering Frontiers in Anti-Cancer Drug Development

IF 3.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Sukanya Sonowal, Kalyani Pathak, Dibyajyoti Das, Kabyashree Buragohain, Ankita Gogoi, Nikha Borah, Aparoop Das, Ratul Nath
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Abstract

Cancer remains a persistent global health concern, representing a significant challenge in medical science and patient care. In this context, l-asparaginase has emerged as a promising therapeutic agent due to its unique ability to deplete circulating asparagine, thereby selectively targeting cancer cells. However, despite its potential, current formulations of l-asparaginase are not without limitations. Issues such as immunogenicity, short half-life, and variable efficacy present hurdles in its widespread clinical application. To overcome these hurdles, researchers are focusing on developing bio-better versions of l-asparaginase. These bio-betters aim to enhance stability, reduce immunogenicity, and optimize enzyme kinetics, thus improving treatment outcomes. This review critically assesses the current landscape of l-asparaginase bio-betters, offering insights into ongoing formulations and advancements, optimization strategies, and future bio-engineering frontiers. It discusses modifications to enhance therapeutic properties and explores innovative approaches like in-silico enzyme engineering and artificial intelligence, highlighting their potential to improve the therapeutic profile of l-asparaginase. Challenges and debates surrounding the l-asparaginase mechanism are also addressed. By addressing current challenges and outlining future directions, this review aims to contribute to the advancement of anti-cancer therapeutics, particularly in the context of l-asparaginase bio-better research.

Abstract Image

Abstract Image

l-Asparaginase Bio-Betters:洞察抗癌药物开发中的现有配方、优化策略和未来生物工程前沿
癌症仍然是全球持续关注的健康问题,是医学科学和病人护理方面的重大挑战。在这种情况下,l-天冬酰胺酶因其消耗循环中天冬酰胺的独特能力,从而有选择性地靶向癌细胞,成为一种很有前景的治疗药物。然而,尽管l-天冬酰胺酶具有潜力,但其目前的制剂并非没有局限性。免疫原性、半衰期短和疗效不稳定等问题阻碍了它在临床上的广泛应用。为了克服这些障碍,研究人员正致力于开发更好的 l-天冬酰胺酶生物制剂。这些生物替代品旨在提高稳定性、降低免疫原性和优化酶动力学,从而改善治疗效果。本综述对目前的 l-天冬酰胺酶生物制剂进行了严格评估,深入探讨了正在进行的配方和进展、优化策略以及未来的生物工程前沿。文章讨论了为增强治疗特性而进行的改良,并探讨了诸如硅内酶工程和人工智能等创新方法,强调了它们在改善 l-天冬酰胺酶治疗特性方面的潜力。报告还探讨了围绕 l-天冬酰胺酶机制的挑战和争论。通过探讨当前的挑战和概述未来的方向,这篇综述旨在为抗癌疗法的发展做出贡献,尤其是在 l-天冬酰胺酶生物改进研究方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advanced Therapeutics
Advanced Therapeutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.10
自引率
2.20%
发文量
130
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