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荧光原位杂交(FISH)联合形态学、免疫表型及细胞遗传学分析在阿曼儿童/成人急性淋巴细胞白血病患者中的重要性

Importance of FISH combined with Morphology, Immunophenotype and Cytogenetic Analysis of Childhood/ Adult Acute Lymphoblastic Leukemia in Omani Patients.

作者信息

Goud Tadakal Mallana, Al Salmani Kamla Khalfan, Al Harasi Salma Mohammed, Al Musalhi Muhanna, Wasifuddin Shah Mohammed, Rajab Anna

机构信息

National Genetic Centre, Muscat, Sultanate of Oman E-mail :

出版信息

Asian Pac J Cancer Prev. 2015;16(16):7343-50. doi: 10.7314/apjcp.2015.16.16.7343.

Abstract

Genetic changes associated with acute lymphoblastic leukemia (ALL) provide very important diagnostic and prognostic information with a direct impact on patient management. Detection of chromosome abnormalities by conventional cytogenetics combined with fluorescence in situ hybridization (FISH) play a very significant role in assessing risk stratification. Identification of specific chromosome abnormalities has led to the recognition of genetic subgroups based on reciprocal translocations, deletions and modal number in B or T-cell ALL. In the last twelve years 102 newly diagnosed childhood/adult ALL bone marrow samples were analysed for chromosomal abnormalities with conventional G-banding, and FISH (selected cases) using specific probes in our hospital. G-banded karyotype analysis found clonal numerical and/or structural chromosomal aberrations in 74.2% of cases. Patients with pseudodiploidy represented the most frequent group (38.7%) followed by high hyperdiploidy group (12.9%), low hyperdiploidy group (9.7%), hypodiploidy (<46) group (9.7%) and high hypertriploidy group (3.2%). The highest observed numerical chromosomal alteration was high hyperdiploidy (12.9%) with abnormal karyotypes while abnormal 12p (7.5%) was the highest observed structural abnormality followed by t(12;21)(p13.3;q22) resulting in ETV6/RUNX1 fusion (5.4%) and t(9;22)(q34.1;q11.2) resulting in BCR/ABL1 fusion (4.3%). Interestingly, we identified 16 cases with rare and complex structural aberrations. Application of the FISH technique produced major improvements in the sensitivity and accuracy of cytogenetic analysis with ALL patients. In conclusion it confirmed heterogeneity of ALL by identifying various recurrent chromosomal aberrations along with non-specific rearrangements and their association with specific immunophenotypes. This study pool is representative of paediatric/adult ALL patients in Oman.

摘要

与急性淋巴细胞白血病(ALL)相关的基因变化提供了非常重要的诊断和预后信息,对患者管理有直接影响。通过传统细胞遗传学结合荧光原位杂交(FISH)检测染色体异常在评估风险分层中起着非常重要的作用。特定染色体异常的鉴定导致了基于B或T细胞ALL中的相互易位、缺失和核型数目的基因亚组的识别。在过去十二年中,我们医院使用特定探针,通过传统G显带和FISH(部分病例)对102例新诊断的儿童/成人ALL骨髓样本进行了染色体异常分析。G显带核型分析在74.2%的病例中发现了克隆性数目和/或结构染色体畸变。假二倍体患者是最常见的组(38.7%),其次是高超二倍体组(12.9%)、低超二倍体组(9.7%)、亚二倍体(<46)组(9.7%)和高超三倍体组(3.2%)。观察到的最高数目染色体改变是核型异常的高超二倍体(12.9%),而异常12p(7.5%)是观察到的最高结构异常,其次是导致ETV6/RUNX1融合的t(12;21)(p13.3;q22)(5.4%)和导致BCR/ABL1融合的t(9;22)(q34.1;q11.2)(4.3%)。有趣的是,我们鉴定出16例具有罕见和复杂结构畸变的病例。FISH技术的应用极大地提高了ALL患者细胞遗传学分析的敏感性和准确性。总之,它通过识别各种复发性染色体畸变以及非特异性重排及其与特定免疫表型的关联,证实了ALL的异质性。该研究样本代表了阿曼的儿科/成人ALL患者。

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