• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
NUDT15 c.415C>T increases risk of 6-mercaptopurine induced myelosuppression during maintenance therapy in children with acute lymphoblastic leukemia.NUDT15基因c.415C>T位点变异增加了急性淋巴细胞白血病患儿维持治疗期间6-巯基嘌呤诱导的骨髓抑制风险。
Haematologica. 2016 Jan;101(1):e24-6. doi: 10.3324/haematol.2015.134775. Epub 2015 Sep 24.
2
NUDT15 gene polymorphism related to mercaptopurine intolerance in Taiwan Chinese children with acute lymphoblastic leukemia.台湾华裔急性淋巴细胞白血病儿童中与巯嘌呤不耐受相关的NUDT15基因多态性
Pharmacogenomics J. 2016 Nov;16(6):536-539. doi: 10.1038/tpj.2015.75. Epub 2015 Oct 27.
3
Polymorphism and Its Association With Mercaptopurine Hematotoxicity in Acute Lymphoblastic Leukemia in Indonesian Children.多态性及其与印度尼西亚儿童急性淋巴细胞白血病巯基嘌呤血液毒性的关系。
In Vivo. 2024 Jul-Aug;38(4):2041-2048. doi: 10.21873/invivo.13662.
4
Determination of NUDT15 variants by targeted sequencing can identify compound heterozygosity in pediatric acute lymphoblastic leukemia patients.通过靶向测序确定 NUDT15 变异可鉴定儿科急性淋巴细胞白血病患者的复合杂合性。
Sci Rep. 2020 Sep 1;10(1):14400. doi: 10.1038/s41598-020-71468-y.
5
Effect of NUDT15 on incidence of neutropenia in children with acute lymphoblastic leukemia.NUDT15对急性淋巴细胞白血病患儿中性粒细胞减少症发生率的影响。
Pediatr Int. 2019 Aug;61(8):754-758. doi: 10.1111/ped.13905. Epub 2019 Aug 14.
6
Association of gene polymorphism with adverse reaction, treatment efficacy, and dose of 6-mercaptopurine in patients with acute lymphoblastic leukemia: a systematic review and meta-analysis.基因多态性与急性淋巴细胞白血病患者不良反应、治疗效果和 6-巯基嘌呤剂量的相关性:系统评价和荟萃分析。
Haematologica. 2024 Apr 1;109(4):1053-1068. doi: 10.3324/haematol.2023.282761.
7
Optimal predictor for 6-mercaptopurine intolerance in Chinese children with acute lymphoblastic leukemia: NUDT15, TPMT, or ITPA genetic variants?中国儿童急性淋巴细胞白血病中巯嘌呤不耐受的最佳预测因子:NUDT15、TPMT 还是 ITPA 基因突变?
BMC Cancer. 2018 May 2;18(1):516. doi: 10.1186/s12885-018-4398-2.
8
genetic variants are related to thiopurine-induced neutropenia in Thai children with acute lymphoblastic leukemia.遗传变异与泰国急性淋巴细胞白血病儿童使用硫唑嘌呤引起的中性粒细胞减少有关。
Pharmacogenomics. 2020 Apr;21(6):403-410. doi: 10.2217/pgs-2019-0177. Epub 2020 Apr 20.
9
Genotyping NUDT15 can predict the dose reduction of 6-MP for children with acute lymphoblastic leukemia especially at a preschool age.对NUDT15进行基因分型可以预测急性淋巴细胞白血病患儿尤其是学龄前儿童6-巯基嘌呤的剂量降低情况。
J Hum Genet. 2016 Sep;61(9):797-801. doi: 10.1038/jhg.2016.55. Epub 2016 May 19.
10
NUDT15 and TPMT genetic polymorphisms are related to 6-mercaptopurine intolerance in children treated for acute lymphoblastic leukemia at the Children's Cancer Center of Lebanon.NUDT15和TPMT基因多态性与黎巴嫩儿童癌症中心接受急性淋巴细胞白血病治疗的儿童对6-巯基嘌呤不耐受有关。
Pediatr Blood Cancer. 2017 Jan;64(1):146-150. doi: 10.1002/pbc.26189. Epub 2016 Aug 31.

引用本文的文献

1
Exploring the Pharmacogenomic Map of Croatia: PGx Clustering of 522-Patient Cohort Based on UMAP + HDBSCAN Algorithm.探索克罗地亚的药物基因组图谱:基于UMAP + HDBSCAN算法对522名患者队列进行药物基因组学聚类分析。
Int J Mol Sci. 2025 Jan 12;26(2):589. doi: 10.3390/ijms26020589.
2
Polymorphism and Its Association With Mercaptopurine Hematotoxicity in Acute Lymphoblastic Leukemia in Indonesian Children.多态性及其与印度尼西亚儿童急性淋巴细胞白血病巯基嘌呤血液毒性的关系。
In Vivo. 2024 Jul-Aug;38(4):2041-2048. doi: 10.21873/invivo.13662.
3
Association of gene polymorphism with adverse reaction, treatment efficacy, and dose of 6-mercaptopurine in patients with acute lymphoblastic leukemia: a systematic review and meta-analysis.基因多态性与急性淋巴细胞白血病患者不良反应、治疗效果和 6-巯基嘌呤剂量的相关性:系统评价和荟萃分析。
Haematologica. 2024 Apr 1;109(4):1053-1068. doi: 10.3324/haematol.2023.282761.
4
Genetic variants of genes involved in thiopurine metabolism pathway are associated with 6-mercaptopurine toxicity in pediatric acute lymphoblastic leukemia patients from Ethiopia.参与硫嘌呤代谢途径的基因的遗传变异与埃塞俄比亚儿童急性淋巴细胞白血病患者的6-巯基嘌呤毒性相关。
Front Pharmacol. 2023 May 9;14:1159307. doi: 10.3389/fphar.2023.1159307. eCollection 2023.
5
Pharmacogenetics implementation in the clinics: information and guidelines for germline variants.临床中的药物遗传学应用:种系变异的信息与指南
Cancer Drug Resist. 2019 Mar 19;2(1):53-68. doi: 10.20517/cdr.2018.25. eCollection 2019.
6
Genetic Variants in Chinese Han, Uighur, Kirghiz, and Dai Nationalities.中国汉族、维吾尔族、柯尔克孜族和傣族的基因变异
Front Pediatr. 2022 Apr 14;10:832363. doi: 10.3389/fped.2022.832363. eCollection 2022.
7
Effect of ITPA Polymorphism on Adverse Drug Reactions of 6-Mercaptopurine in Pediatric Patients with Acute Lymphoblastic Leukemia: A Systematic Review and Meta-Analysis.ITPA基因多态性对儿童急性淋巴细胞白血病患者6-巯基嘌呤药物不良反应的影响:一项系统评价和荟萃分析
Pharmaceuticals (Basel). 2022 Mar 29;15(4):416. doi: 10.3390/ph15040416.
8
Susceptibility to thiopurine toxicity by and variants in Colombian children with acute lymphoblastic leukemia.哥伦比亚急性淋巴细胞白血病患儿中 和 变异体对硫嘌呤毒性的易感性。
Colomb Med (Cali). 2021 Sep 30;52(3):e2074569. doi: 10.25100/cm.v52i3.4569. eCollection 2021 Jul-Sep.
9
[Effect of genetic polymorphism of TPMT and NUDT15 on the tolerance of 6-mercaptopurine therapy in adult acute lymphoblastic leukemia].[TPMT和NUDT15基因多态性对成人急性淋巴细胞白血病6-巯基嘌呤治疗耐受性的影响]
Zhonghua Xue Ye Xue Za Zhi. 2021 Nov 14;42(11):911-916. doi: 10.3760/cma.j.issn.0253-2727.2021.11.005.
10
Meta-Analysis of Genetic Polymorphism on Thiopurine-Induced Myelosuppression in Asian Populations.亚洲人群中硫嘌呤诱导骨髓抑制的基因多态性的Meta分析。
Front Pharmacol. 2021 Dec 2;12:784712. doi: 10.3389/fphar.2021.784712. eCollection 2021.

本文引用的文献

1
Susceptibility to 6-MP toxicity conferred by a NUDT15 variant in Japanese children with acute lymphoblastic leukaemia.日本急性淋巴细胞白血病儿童中NUDT15变异导致的6-巯基嘌呤毒性易感性。
Br J Haematol. 2015 Oct;171(1):109-15. doi: 10.1111/bjh.13518. Epub 2015 Jun 2.
2
Inherited NUDT15 variant is a genetic determinant of mercaptopurine intolerance in children with acute lymphoblastic leukemia.遗传性NUDT15变异是急性淋巴细胞白血病患儿巯嘌呤不耐受的遗传决定因素。
J Clin Oncol. 2015 Apr 10;33(11):1235-42. doi: 10.1200/JCO.2014.59.4671. Epub 2015 Jan 26.
3
Outcome of acute lymphoblastic leukemia treatment using national protocols at the Queen Sirikit National Institute of Child Health.
J Med Assoc Thai. 2014 Jun;97 Suppl 6:S1-5.
4
A common missense variant in NUDT15 confers susceptibility to thiopurine-induced leukopenia.NUDT15基因中的一种常见错义变异会使人易患硫嘌呤诱导的白细胞减少症。
Nat Genet. 2014 Sep;46(9):1017-20. doi: 10.1038/ng.3060. Epub 2014 Aug 10.
5
Mercaptopurine/Methotrexate maintenance therapy of childhood acute lymphoblastic leukemia: clinical facts and fiction.巯嘌呤/甲氨蝶呤维持治疗儿童急性淋巴细胞白血病:临床的真相与假象
J Pediatr Hematol Oncol. 2014 Oct;36(7):503-17. doi: 10.1097/MPH.0000000000000206.
6
Implementation of TPMT testing.硫嘌呤甲基转移酶(TPMT)检测的实施
Br J Clin Pharmacol. 2014 Apr;77(4):704-14. doi: 10.1111/bcp.12226.
7
Children's Oncology Group's 2013 blueprint for research: acute lymphoblastic leukemia.儿童肿瘤学组 2013 年研究蓝图:急性淋巴细胞白血病。
Pediatr Blood Cancer. 2013 Jun;60(6):957-63. doi: 10.1002/pbc.24420. Epub 2012 Dec 19.
8
The activity of the inosine triphosphate pyrophosphatase affects toxicity of 6-mercaptopurine during maintenance therapy for acute lymphoblastic leukemia in Japanese children.肌苷三磷酸焦磷酸酶的活性会影响日本儿童急性淋巴细胞白血病维持治疗期间 6-巯基嘌呤的毒性。
Leuk Res. 2012 May;36(5):560-4. doi: 10.1016/j.leukres.2011.11.015. Epub 2011 Dec 24.
9
Polymorphism of ITPA 94C>A and risk of adverse effects among patients with acute lymphoblastic leukaemia treated with 6-mercaptopurine.ITPA 94C>A 多态性与接受 6-巯基嘌呤治疗的急性淋巴细胞白血病患者不良事件风险的关系。
J Clin Pharm Ther. 2012 Apr;37(2):237-41. doi: 10.1111/j.1365-2710.2011.01272.x. Epub 2011 May 5.
10
Impact of the heterozygous TPMT*1/*3C genotype on azathioprine-induced myelosuppression in kidney transplant recipients in Thailand.杂合子TPMT*1/*3C基因型对泰国肾移植受者硫唑嘌呤诱导的骨髓抑制的影响。
Clin Ther. 2009 Jul;31(7):1524-33. doi: 10.1016/j.clinthera.2009.07.008.

NUDT15 c.415C>T increases risk of 6-mercaptopurine induced myelosuppression during maintenance therapy in children with acute lymphoblastic leukemia.

作者信息

Chiengthong Kanhatai, Ittiwut Chupong, Muensri Sasipa, Sophonphan Jiratchaya, Sosothikul Darintr, Seksan Panya, Suppipat Koramit, Suphapeetiporn Kanya, Shotelersuk Vorasuk

机构信息

Division of Pediatric Hematology and Oncology, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok.

Central Laboratory, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok.

出版信息

Haematologica. 2016 Jan;101(1):e24-6. doi: 10.3324/haematol.2015.134775. Epub 2015 Sep 24.

DOI:10.3324/haematol.2015.134775
PMID:26405151
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4697903/
Abstract
摘要