基因诊断对急性淋巴细胞白血病(ALL)治疗和预后的重要性- 1例报告

Mateusz Raniewicz, Maciej Dubaj, Karol Bigosiński, Aleksandra Dembowska, Małgorzata Mitura-Lesiuk
{"title":"基因诊断对急性淋巴细胞白血病(ALL)治疗和预后的重要性- 1例报告","authors":"Mateusz Raniewicz, Maciej Dubaj, Karol Bigosiński, Aleksandra Dembowska, Małgorzata Mitura-Lesiuk","doi":"10.5603/mrj.96967","DOIUrl":null,"url":null,"abstract":"Acute lymphoblastic leukaemia (ALL) is the most common malignancy among children. It originates from over-proliferating immature lymphoid cells called lymphoblasts. Modern genetic studies have shown that the aetiology of ALL is correlated with numerous chromosomal aberrations, including activating mutation of the JAK/STAT pathway. This pathway is responsible for regulating the transmission of signals from extracellular cytokines to the nucleus of cells, regulating their growth, differentiation and immune response. With proper patient diagnosis, it is possible to correctly classify the genetic subtypes of ALL, allowing more effective therapies to be introduced. The following study presents the importance of genetic diagnosis for the treatment of a paediatric patient with ALL with the above mutation in the genome.","PeriodicalId":18485,"journal":{"name":"Medical Research Journal","volume":"41 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Importance of genetic diagnosis for treatment and prognosis in acute lymphoblastic leukaemia (ALL) — a case report\",\"authors\":\"Mateusz Raniewicz, Maciej Dubaj, Karol Bigosiński, Aleksandra Dembowska, Małgorzata Mitura-Lesiuk\",\"doi\":\"10.5603/mrj.96967\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Acute lymphoblastic leukaemia (ALL) is the most common malignancy among children. It originates from over-proliferating immature lymphoid cells called lymphoblasts. Modern genetic studies have shown that the aetiology of ALL is correlated with numerous chromosomal aberrations, including activating mutation of the JAK/STAT pathway. This pathway is responsible for regulating the transmission of signals from extracellular cytokines to the nucleus of cells, regulating their growth, differentiation and immune response. With proper patient diagnosis, it is possible to correctly classify the genetic subtypes of ALL, allowing more effective therapies to be introduced. The following study presents the importance of genetic diagnosis for the treatment of a paediatric patient with ALL with the above mutation in the genome.\",\"PeriodicalId\":18485,\"journal\":{\"name\":\"Medical Research Journal\",\"volume\":\"41 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-10-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medical Research Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5603/mrj.96967\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical Research Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5603/mrj.96967","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

急性淋巴细胞白血病(ALL)是儿童最常见的恶性肿瘤。它起源于过度增殖的未成熟淋巴样细胞,称为淋巴母细胞。现代遗传学研究表明,ALL的病因与多种染色体畸变相关,包括JAK/STAT通路的激活突变。该通路负责调节细胞外细胞因子向细胞核的信号传递,调节细胞的生长、分化和免疫应答。通过适当的患者诊断,可以对ALL的遗传亚型进行正确分类,从而引入更有效的治疗方法。下面的研究提出了基因诊断的重要性,以治疗儿科患者与上述突变的基因组。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Importance of genetic diagnosis for treatment and prognosis in acute lymphoblastic leukaemia (ALL) — a case report
Acute lymphoblastic leukaemia (ALL) is the most common malignancy among children. It originates from over-proliferating immature lymphoid cells called lymphoblasts. Modern genetic studies have shown that the aetiology of ALL is correlated with numerous chromosomal aberrations, including activating mutation of the JAK/STAT pathway. This pathway is responsible for regulating the transmission of signals from extracellular cytokines to the nucleus of cells, regulating their growth, differentiation and immune response. With proper patient diagnosis, it is possible to correctly classify the genetic subtypes of ALL, allowing more effective therapies to be introduced. The following study presents the importance of genetic diagnosis for the treatment of a paediatric patient with ALL with the above mutation in the genome.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信