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慢性粒细胞白血病患者骨髓和外周血细胞荧光原位杂交(FISH)及G显带的可靠性评估

Reliability Evaluation of Fluorescence In Situ Hybridization (FISH) and G-Banding on Bone Marrow and Peripheral Blood Cells in Chronic Myelogenous Leukemia Patients.

作者信息

Manaflouyan Khajehmarjany Soheila, Rahmani Seyed Ali, Chavoshi Seyed Hadi, Esfahani Ali, Movassaghpour Akbari Ali Akbar

机构信息

Department of Cellular and Molecular Biology, Islamic Azad University, Ahar Branch, East Azerbaijan, Iran ; Dr. Rahmani Medical Genetic Lab, Tabriz, East Azerbaijan, Iran.

Department of Hematology and Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, East Azerbaijan, Iran ; Emam Reza Hospital, Tabriz, East Azerbaijan, Iran.

出版信息

Cell J. 2015 Spring;17(1):171-80. doi: 10.22074/cellj.2015.525. Epub 2015 Apr 8.

DOI:10.22074/cellj.2015.525
PMID:25870848
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4393667/
Abstract

Chronic myeloid leukemia (CML) is a myeloproliferative disease. The cytogenetic hallmark of CML is Philadelphia (Ph) chromosome. This study aimed to diagnose suspected CML patients, to monitor CML patients under therapy using cytogenetic and fluorescence in situ hybridization (FISH) techniques to analyze their bone marrow (BM) and peripheral blood (PB) samples, and finally to compare their obtained results for both specimens. This study was conducted during one-year period (2012-2013). The participants were recruited from the Hematology and Oncology Clinic of Shahid Gazi (Emam Reza) Hospital of Tabriz University of Medical Sciences, Tabriz, East Azerbaijan Province, Iran. We analyzed 90 samples from 60 suspected CML patients (30 BM and 60 PB samples). All samples were analyzed using G-banding, 5 samples using dual fusion FISH (DF-FISH) probes, as well as 30 samples using both FISH and G-banding. Among the 90 analyzed samples of 60 patients, 25 (41.66%) were Ph+ using karyotyping, whereas five cases were not analyzable, so FISH was applied and the results confirmed that only two individuals were BCR-ABL+. In the comparison between 25 BM and 25 PB samples using karyotyping, 15 (60%) and 10 (40%) were ph+, respectively. The comparison of FISH and karyotyping on 30 samples showed that 9 (30%) and 8 (26.66%) were Ph+, respectively, and only 18.18% of Ph+ patients showed atypical patterns. In the comparison between BM-cytogenetic and PB- interphase-FISH (I-FISH), BM-cytogenetic was more reliable than PB-I-FISH in detecting Ph. Our data demonstrate that FISH analysis is a rapid, reliable and sensitive technique. The comparison between BM and PB showed that PB can not be replaced by BM, even in detecting by FISH.

摘要

慢性髓性白血病(CML)是一种骨髓增殖性疾病。CML的细胞遗传学标志是费城(Ph)染色体。本研究旨在诊断疑似CML患者,使用细胞遗传学和荧光原位杂交(FISH)技术分析其骨髓(BM)和外周血(PB)样本,以监测接受治疗的CML患者,最后比较两种标本的检测结果。本研究在一年期间(2012 - 2013年)进行。参与者来自伊朗东阿塞拜疆省大不里士医科大学沙希德加齐(伊玛目礼萨)医院的血液学和肿瘤学诊所。我们分析了60例疑似CML患者的90份样本(30份BM样本和60份PB样本)。所有样本均采用G显带分析,5份样本采用双融合FISH(DF - FISH)探针分析,30份样本同时采用FISH和G显带分析。在60例患者的90份分析样本中,25份(41.66%)核型分析为Ph +,而5例无法分析,因此采用FISH检测,结果证实只有2例为BCR - ABL +。在使用核型分析比较25份BM样本和25份PB样本时,Ph +分别为15份(60%)和10份(40%)。对30份样本进行FISH和核型分析比较显示,Ph +分别为9份(30%)和8份(26.66%),仅18.18%的Ph +患者表现出非典型模式。在BM细胞遗传学与PB间期FISH(I - FISH)的比较中,BM细胞遗传学在检测Ph方面比PB - I - FISH更可靠。我们的数据表明,FISH分析是一种快速、可靠且灵敏的技术。BM与PB的比较表明,即使在FISH检测中,PB也不能被BM替代。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9950/4393667/76bbc816482e/Cell-J-17-171-g07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9950/4393667/e7a34d582f56/Cell-J-17-171-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9950/4393667/67a3e6ed8687/Cell-J-17-171-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9950/4393667/bbd8b8aa5bcd/Cell-J-17-171-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9950/4393667/141eccd86d19/Cell-J-17-171-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9950/4393667/e8cd15119111/Cell-J-17-171-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9950/4393667/b04361d149e7/Cell-J-17-171-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9950/4393667/76bbc816482e/Cell-J-17-171-g07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9950/4393667/e7a34d582f56/Cell-J-17-171-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9950/4393667/67a3e6ed8687/Cell-J-17-171-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9950/4393667/bbd8b8aa5bcd/Cell-J-17-171-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9950/4393667/141eccd86d19/Cell-J-17-171-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9950/4393667/e8cd15119111/Cell-J-17-171-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9950/4393667/b04361d149e7/Cell-J-17-171-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9950/4393667/76bbc816482e/Cell-J-17-171-g07.jpg

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本文引用的文献

1
Molecular biology of bcr-abl1-positive chronic myeloid leukemia.bcr-abl1 阳性慢性髓性白血病的分子生物学
Blood. 2009 Feb 19;113(8):1619-30. doi: 10.1182/blood-2008-03-144790. Epub 2008 Sep 30.
2
"Home-brew" FISH assay shows higher efficiency than BCR-ABL dual color, dual fusion probe in detecting microdeletions and complex rearrangements associated with t(9;22) in chronic myeloid leukemia.“自制”荧光原位杂交(FISH)检测法在检测慢性髓性白血病中与t(9;22)相关的微缺失和复杂重排方面,比BCR-ABL双色双融合探针具有更高的效率。
Cancer Genet Cytogenet. 2007 Apr 15;174(2):121-6. doi: 10.1016/j.cancergencyto.2006.09.025.
3
Introduction: chronic myelogenous leukemia (CML).
Semin Hematol. 2007 Jan;44(1 Suppl 1):S1-3. doi: 10.1053/j.seminhematol.2006.12.001.
4
The incidence and patterns of BCR/ABL rearrangements in chronic myeloid leukaemia (CML) using fluorescence in situ hybridisation (FISH).采用荧光原位杂交(FISH)技术检测慢性髓性白血病(CML)中BCR/ABL重排的发生率及模式。
Ann Acad Med Singap. 2005 Oct;34(9):533-8.
5
FISH for BCR-ABL on interphases of peripheral blood neutrophils but not of unselected white cells correlates with bone marrow cytogenetics in CML patients treated with imatinib.
Leukemia. 2003 Oct;17(10):1925-9. doi: 10.1038/sj.leu.2403077.
6
High reliability and sensitivity of the BCR/ABL1 D-FISH test for the detection of BCR/ABL rearrangements.用于检测BCR/ABL重排的BCR/ABL1 D-FISH检测具有高可靠性和高灵敏度。
Ann Hematol. 2002 Mar;81(3):147-53. doi: 10.1007/s00277-001-0424-5. Epub 2002 Feb 23.
7
Cytogenetics of chronic myeloid leukaemia.慢性髓性白血病的细胞遗传学
Best Pract Res Clin Haematol. 2001 Sep;14(3):553-71. doi: 10.1053/beha.2001.0154.
8
Fluorescence in situ hybridization: uses and limitations.荧光原位杂交:用途与局限性
Semin Hematol. 2000 Oct;37(4):320-33. doi: 10.1016/s0037-1963(00)90013-1.
9
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J Clin Oncol. 2000 Apr;18(7):1533-8. doi: 10.1200/JCO.2000.18.7.1533.
10
The impact of the new fish technologies on the cytogenetics of haematological malignancies.
Br J Haematol. 1999 Mar;104(4):648-58. doi: 10.1046/j.1365-2141.1999.01181.x.