4.6 Review

Novel Insights on the Use of L-Asparaginase as an Efficient and Safe Anti-Cancer Therapy

Journal

CANCERS
Volume 14, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/cancers14040902

Keywords

asparaginase; asparagine; glutamine; acute lymphoblastic leukemia; solid cancers

Categories

Funding

  1. Belgian Foundation Against Cancer
  2. Belgian Stand Up to Cancer Foundation
  3. vzw Kinderkanker fonds
  4. Research Foundation Flanders

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L-asparaginase (L-ASNase) therapy is crucial for pediatric acute lymphoblastic leukemia (ALL), but its use is limited due to high toxicity. Optimized L-ASNase molecules and drug combinations offer potential solutions. Resistance mechanisms and adverse effects of L-ASNase are discussed, along with its potential for treating hematological and solid tumors.
Simple Summary L-asparaginase (L-ASNase) therapy is key for achieving the very high cure rate of pediatric acute lymphoblastic leukemia (ALL), yet its use is mostly confined to this indication. One main reason preventing the expansion of today's FDA-approved L-ASNases to solid cancers is their high toxicity and side effects, which become especially challenging in adult patients. The design of optimized L-ASNase molecules provides opportunities to overcome these unwanted toxicities. An additional challenge to broader application of L-ASNases is how cells can counter the pharmacological effect of this drug and the identification of L-ASNases resistance mechanisms. In this review, we discuss recent insights into L-ASNase adverse effects, resistance mechanisms, and how novel L-ASNase variants and drug combinations can expand its clinical applicability, with a focus on both hematological and solid tumors. L-Asparaginase (L-ASNase) is an enzyme that hydrolyses the amino acid asparagine into aspartic acid and ammonia. Systemic administration of bacterial L-ASNase is successfully used to lower the bioavailability of this non-essential amino acid and to eradicate rapidly proliferating cancer cells with a high demand for exogenous asparagine. Currently, it is a cornerstone drug in the treatment of the most common pediatric cancer, acute lymphoblastic leukemia (ALL). Since these lymphoblasts lack the expression of asparagine synthetase (ASNS), these cells depend on the uptake of extracellular asparagine for survival. Interestingly, recent reports have illustrated that L-ASNase may also have clinical potential for the treatment of other aggressive subtypes of hematological or solid cancers. However, immunogenic and other severe adverse side effects limit optimal clinical use and often lead to treatment discontinuation. The design of optimized and novel L-ASNase formulations provides opportunities to overcome these limitations. In addition, identification of multiple L-ASNase resistance mechanisms, including ASNS promoter reactivation and desensitization, has fueled research into promising novel drug combinations to overcome chemoresistance. In this review, we discuss recent insights into L-ASNase adverse effects, resistance both in hematological and solid tumors, and how novel L-ASNase variants and drug combinations can expand its clinical applicability.

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