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巴基斯坦成年急性淋巴细胞白血病患者中具有预后意义的融合致癌基因及其与疾病生物学和预后的关联。

Prognostically significant fusion oncogenes in Pakistani patients with adult acute lymphoblastic leukemia and their association with disease biology and outcome.

作者信息

Sabir Noreen, Iqbal Zafar, Aleem Aamer, Awan Tashfeen, Naeem Tahir, Asad Sultan, Tahir Ammara H, Absar Muhammad, Hasanato Rana M W, Basit Sulman, Chishti Muhammad Azhar, Faiyaz Ul-Haque Muhammad, Khalid Ahmad Muktar, Sabar Muhammad Farooq, Rasool Mahmood, Karim Sajjad, Khan Mahwish, Samreen Baila, Akram Afia M, Siddiqi Muhammad Hassan, Shahzadi Saba, Shahbaz Sana, Ali Agha Shabbir, Mahmood Amer, Akram Muhammad, Saeed Tariq, Saleem Arsalan, Mohsin Danish, Shah Ijaz Hussain, Khalid Muhammad, Asif Muhammad, Iqbal Mudassar, Akhtar Tanveer

机构信息

Faculty of Biological Sciences, Department of Zoology, University of the Punjab, Lahore, Pakistan.

出版信息

Asian Pac J Cancer Prev. 2012;13(7):3349-55. doi: 10.7314/apjcp.2012.13.7.3349.

Abstract

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-TAL positive patients had frequent organomegaly and usually presented with a platelets count of less than 50 x10(9)/l. 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 of 5 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.

摘要

背景与目的

染色体异常在急性淋巴细胞白血病(ALL)的发生中起重要作用,并具有预后意义。ALL中五个主要的风险分层融合基因是BCR-ABL、MLL-AF4、ETV6-RUNX11、E2A-PBX1和SIL-TAL1。本研究旨在检测成年ALL患者中常见的染色体易位及相关融合癌基因,并研究它们与临床特征及治疗结局的关系。

方法

我们在诊断时采用逆转录聚合酶链反应(RT-PCR)和间期荧光原位杂交(interphase-FISH)研究了104例成年ALL患者中的融合癌基因,以及它们与临床特征和治疗结局的关联。

结果

在82/104(79%)例患者中发现了五个最常见的融合基因,即BCR-ABL(t(9;22))、TCF3-PBX1(t(1;19))、ETV6-RUNX1(t(12;21))、MLL-AF4(t(4;11))和SIL-TAL1(Del 1p32)。TCF3-PBX1融合基因与淋巴结病相关,SIL-TAL1阳性患者常有器官肿大,且血小板计数通常低于50×10⁹/L。与携带其他基因的患者相比,ETV6-RUNX1融合基因阳性患者的生存率更高。MLL-AF4和BCR-ABL阳性是一部分具有侵袭性临床行为和不良结局的成年ALL患者的特征。

结论

这是来自巴基斯坦的第一项研究,调查了成年ALL患者中5种融合癌基因的频率,以及它们与临床特征、治疗反应和结局的关联。一些癌基因的频率与其他地方报道的不同,且它们似乎与不同的临床特征和治疗结局相关。这些信息将有助于成年ALL患者的预后分层和风险适应性管理。

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