Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Mol Cancer Ther. 2019 Sep;18(9):1587-1592. doi: 10.1158/1535-7163.MCT-18-1329. Epub 2019 Jun 17.
We and others have reported that the anticancer activity of L-asparaginase (ASNase) against asparagine synthetase (ASNS)-positive cell types requires ASNase glutaminase activity, whereas anticancer activity against ASNS-negative cell types does not. Here, we attempted to disentangle the relationship between asparagine metabolism, glutamine metabolism, and downstream pathways that modulate cell viability by testing the hypothesis that ASNase anticancer activity is based on asparagine depletion rather than glutamine depletion per se. We tested ASNase wild-type (ASNase) and its glutaminase-deficient Q59L mutant (ASNase) and found that ASNase glutaminase activity contributed to durable anticancer activity against xenografts of the ASNS-negative Sup-B15 leukemia cell line in NOD/SCID gamma mice, whereas asparaginase activity alone yielded a mere growth delay. Our findings suggest that ASNase glutaminase activity is necessary for durable, single-agent anticancer activity , even against ASNS-negative cancer types.
我们和其他人已经报道过,天冬酰胺酶(ASNase)对天冬酰胺合成酶(ASNS)阳性细胞类型的抗癌活性需要 ASNase 谷氨酰胺酶活性,而对 ASNS 阴性细胞类型的抗癌活性则不需要。在这里,我们通过测试以下假设来试图厘清天冬酰胺代谢、谷氨酰胺代谢和调节细胞活力的下游途径之间的关系,即 ASNase 的抗癌活性是基于天冬酰胺的消耗,而不是谷氨酰胺的消耗本身。我们测试了 ASNase 野生型(ASNase)及其谷氨酰胺酶缺陷型 Q59L 突变体(ASNase),发现 ASNase 谷氨酰胺酶活性有助于 NOD/SCID γ 小鼠异种移植的 ASNS 阴性 Sup-B15 白血病细胞系的持久抗癌活性,而单独的天冬酰胺酶活性仅导致生长延迟。我们的研究结果表明,ASNase 谷氨酰胺酶活性对于持久的单药抗癌活性是必要的,即使针对 ASNS 阴性的癌症类型也是如此。