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一种可变剪接的功能获得性NT5C2亚型促成急性淋巴细胞白血病的化疗耐药。

An Alternatively Spliced Gain-of-Function NT5C2 Isoform Contributes to Chemoresistance in Acute Lymphoblastic Leukemia.

作者信息

Torres-Diz Manuel, Reglero Clara, Falkenstein Catherine D, Castro Annette, Hayer Katharina E, Radens Caleb M, Quesnel-Vallières Mathieu, Ang Zhiwei, Sehgal Priyanka, Li Marilyn M, Barash Yoseph, Tasian Sarah K, Ferrando Adolfo, Thomas-Tikhonenko Andrei

出版信息

bioRxiv. 2024 Jul 22:2023.09.14.557413. doi: 10.1101/2023.09.14.557413.

DOI:10.1101/2023.09.14.557413
PMID:39091882
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11291008/
Abstract

Relapsed or refractory B-cell acute lymphoblastic leukemia (B-ALL) is a major cause of pediatric cancer-related deaths. Relapse-specific mutations do not account for all chemotherapy failures in B- ALL patients, suggesting additional mechanisms of resistance. By mining RNA-seq datasets of paired diagnostic/relapse pediatric B-ALL samples, we discovered pervasive alternative splicing (AS) patterns linked to relapse and affecting drivers of resistance to glucocorticoids, anti-folates, and thiopurines. Most splicing variations represented cassette exon skipping, "poison" exon inclusion, and intron retention, phenocopying well-documented loss-of-function mutations. In contrast, relapse-associated AS of NT5C2 mRNA yielded an isoform with the functionally uncharacterized in-frame exon 6a. Incorporation of the 8-amino acid sequence SQVAVQKR into this enzyme created a putative phosphorylation site and resulted in elevated nucleosidase activity, which is a known consequence of gain-of-function mutations in NT5C2 and a common determinant of 6-mercaptopurine (6-MP) resistance. Consistent with this finding, NT5C2ex6a and the R238W hotspot variant conferred comparable levels of resistance to 6-MP in B-ALL cells both in vitro and in vivo. Furthermore, both the NT5C2ex6a and R238W variants induced collateral sensitivity to the inosine monophosphate dehydrogenase (IMPDH) inhibitor mizoribine. These results ascribe an important role for splicing perturbations in chemotherapy resistance in relapsed B-ALL and suggest that IMPDH inhibitors, including the commonly used immunosuppressive agent mycophenolate mofetil, could be a valuable therapeutic option for treating thiopurine-resistant leukemias.

摘要

复发或难治性B细胞急性淋巴细胞白血病(B-ALL)是儿童癌症相关死亡的主要原因。复发特异性突变并不能解释B-ALL患者所有的化疗失败情况,这表明存在其他耐药机制。通过挖掘配对的诊断/复发儿童B-ALL样本的RNA测序数据集,我们发现了与复发相关的普遍可变剪接(AS)模式,这些模式影响对糖皮质激素、抗叶酸药物和硫嘌呤的耐药驱动因素。大多数剪接变异表现为盒式外显子跳跃、“毒性”外显子包含和内含子保留,模拟了记录充分的功能丧失突变。相比之下,NT5C2 mRNA的复发相关AS产生了一种具有功能未明确的框内外显子6a的异构体。将8个氨基酸序列SQVAVQKR整合到这种酶中产生了一个假定的磷酸化位点,并导致核苷酶活性升高,这是NT5C2功能获得性突变的已知结果,也是6-巯基嘌呤(6-MP)耐药的常见决定因素。与这一发现一致,NT5C2ex6a和R238W热点变体在体外和体内对B-ALL细胞赋予了相当水平的6-MP耐药性。此外,NT5C2ex6a和R238W变体均诱导了对肌苷单磷酸脱氢酶(IMPDH)抑制剂米唑立宾的协同敏感性。这些结果表明剪接扰动在复发B-ALL的化疗耐药中起重要作用,并提示包括常用免疫抑制剂霉酚酸酯在内的IMPDH抑制剂可能是治疗硫嘌呤耐药白血病的有价值的治疗选择。

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