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Prognostically Significant Fusion Oncogenes in Pakistani Patients with Adult Acute Lymphoblastic Leukemia and their Association with Disease Biology and Outcome

机译:预后,巴基斯坦患者成人急性淋巴细胞白血病患者及其与疾病生物学和结果的关联的预后显着的融合

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Background and objectives: Chromosomal abnormalities play an important role in genesis of acute lymphoblastic leukemia (ALL) and have prognostic implications. Five major risk stratifying fusion genes in ALL are BCR-ABL, MLL-AF4, ETV6-RUNX11, E2A-PBX1 and SIL-TAL1. This work aimed to detect common chromosomal translocations and associated fusion oncogenes in adult ALL patients and study their relationship with clinical features and treatment outcome. Methods: We studied fusion oncogenes in 104 adult ALL patients using RT-PCR and interphase-FISH at diagnosis and their association with clinical characteristics and treatment outcome. Results: Five most common fusion genes i.e. BCR-ABL (t 9; 22), TCF3-PBX1 (t 1; 19), ETV6-RUNX1 (t 12; 21), MLL-AF4 (t 4; 11) and SIL-TAL1 (Del 1p32) were found in 82/104 (79%) patients. TCF3-PBX1 fusion gene was associated with lymphadenopathy, SIL-TAL1 positive patients had frequent organomegaly and usually presented with a platelets count of less than . Survival of patients with fusion gene ETV6-RUNX1 was better when compared to patients harboring other genes. MLL-AF4 and BCR-ABL positivity characterized a subset of adult ALL patients with aggressive clinical behaviour and a poor outcome. Conclusions: This is the first study from Pakistan which investigated the frequency of5 fusion oncogenes in adult ALL patients, and their association with clinical features, treatment response and outcome. Frequencies of some of the oncogenes were different from those reported elsewhere and they appear to be associated with distinct clinical characteristics and treatment outcome. This information will help in the prognostic stratification and risk adapted management of adult ALL patients.
机译:背景和目标:染色体异常在急性淋巴细胞白血病(全部)的成因中起重要作用,具有预后的影响。所有的五个主要风险分层融合基因都是BCR-ABL,MLL-AF4,ETV6-RUNX11,E2A-PBX1和SIL-TAL1。这项工作旨在检测成人所有患者的常见染色体易位和相关融合癌症,并研究其与临床特征和治疗结果的关系。方法:通过RT-PCR和诊断诊断和临床特征和治疗结果,研究了104名成人的融合诱导患者的融合孔子生鱼。结果:五种最常见的融合基因IE BCR-ABL(T 9; 22),TCF3-PBX1(T 1; 19),ETV6-RUNX1(T 12; 21),MLL-AF4(T 4; 11)和SIL-在82/104(79%)患者中发现了Tal1(Del 1P32)。 TCF3-PBX1融合基因与淋巴结病有关,SIL-TAL1阳性患者频繁有机大常,通常呈现血小板计数小于。与患有其他基因的患者相比,融合基因Etv6-Runx1患者的存活率更好。 MLL-AF4和BCR-ABL阳性表征成人的一部分,所有患者患有侵略性临床行为和较差的结果。结论:这是巴基斯坦的第一次研究,它研究了成人所有患者的5个融合癌症的频率,及其与临床特征,治疗反应和结果的关联。一些癌基因的频率与其他地方报告的频率不同,它们似乎与不同的临床特征和治疗结果相关。这些信息将有助于预后分层和风险适应成人所有患者的管理。
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