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Application of tri-colour, dual fusion fluorescence in situ hybridization (FISH) system for the characterization of BCR-ABL1 fusion in chronic myelogenous leukaemia (CML) and residual disease monitoring
© Siu et al; licensee BioMed Central Ltd. 2009
Received: 15 January 2009
Accepted: 07 July 2009
Published: 07 July 2009
We studied the application of the BCR-ABL1 + 9q34 tri-colour dual fusion fluorescence in situ hybridization (FISH) system in the characterization of fusion signal pattern and the monitoring of residual disease in chronic myelogenous leukaemia (CML). The signal constellation on metaphases with the tri-colour dual fusion system was defined. The knowledge of various signal patterns obtained from the different genetic rearrangements was further applied to the analysis of hybridization signals on interphase nuclei.
BCR-ABL1 dual colour, dual fusion FISH (D-FISH) was performed on diagnostic samples of 22 CML patients. The tri-colour FISH system was performed on cases that showed aberrant signal patterns other than the classical 1 green (G) 1 orange (O) 2 fusions (F). Using the aqua band-pass filter, random signal overlap in interphase nuclei would be indicated by the presence of an aqua signal (ASS1), while genuine fusion was represented by the absence of the ASS1 signal.
Using the D-FISH system, the signal patterns could be categorized into 4 groups: group 1 (n = 17) showed the classical 1G1O2F; group 2 (n = 2) showed 2G1O1F indicating ABL1 deletion; group 3 (n = 1) showed 1G2O1F indicating BCR deletion; group 4 (n = 2) with 1G1O1F indicating reciprocal ABL1-BCR deletion. The tri-colour dual fusion system correlated with the D-FISH system for cases with der(9) deletion. The added aqua-labelled ASS1 probe was useful in differentiating random signal overlap from genuine BCR-ABL1 fusion in the interphase cells (group 4).
Although the D-FISH probe was valuable in establishing the different patterns of aberrant signals and monitoring patients with the classic 2-fusion signals in CML, the tri-colour dual fusion probe should be used for patients with der(9) deletion to monitor response to treatment.
Chronic myelogenous leukaemia (CML) is a clonal haematopoietic stem cell disorder characterized by the translocation t(9;22)(q34;q11.2). The translocation fuses the 5' sequences of the BCR gene on chromosome 22 with the 3' sequences of the ABL1 gene on the chromosome 9. The dual colour, dual fusion fluorescence in situ hybridization (D-FISH) system can demonstrate the BCR-ABL1 fusion . In classical t(9;22), there is one signal each for the wild type alleles and two fusion signals, one for the fusion gene and the other for the reciprocal product in a positive cell. This dual fusion pattern has provided good analytical sensitivity for the monitoring of disease response to therapy. However, around 15% of CML patients show deletion of the reciprocal ABL1-BCR fusion on the derivative chromosome 9 (der(9) deletion), often with loss of both chromosomes 9 and 22 sequences on either side of the breakpoint [2–4]. The der(9) deletion is associated with an inferior outcome when compared with those without such deletion, but the poor prognosis may at least be partially abrogated by imatinib therapy . In the presence of der(9) deletion, false positivity is a problem with the use of dual colour single or even dual fusion probes. In this study, we have used metaphase FISH to study the signal pattern on diagnostic samples of 22 CML patients. In addition, the BCR-ABL1 + 9q34 tri-colour, dual fusion system was applied on all cases with atypical D-FISH pattern and also in the monitoring of residual disease in a patient with der(9) deletion.
The diagnostic samples, including both peripheral blood and bone marrow from 22 CML patients were retrieved for the study. Cytogenetics study on all the samples showed t(9;22)(q34;q11.2). BCR-ABL1 dual colour dual fusion FISH (D-FISH) (Vysis, Abbott Molecular Inc., IL) was performed on cell pellets kept in Carnoy's fixative that were previously processed for cytogenetics analysis. For cases with aberrant signal pattern other than the classical 1 green (G), 1 orange (O) and 2 fusions (F), the BCR-ABL1 + 9q34 tri-colour dual fusion FISH (Vysis) system was applied to further characterize the signal pattern.
Briefly, cells were dropped onto microscopic slides and aged overnight at 65°C before performing the FISH hybridization procedures according to manufacturer's protocol. 10 μl of the probe mixture was applied to a 18 × 18 mm hybridization area. The hybridized area was sealed with rubber cement to avoid drying in subsequent denaturation and hybridization procedure. The chromosomes and probes were co-denatured at 75°C for 5 minutes and allowed to hybridize overnight at 37°C (Hybridizer, DakoCytomation). Slides were washed in 0.4× SSC/0.3% NP40 at 70°C for 2 minutes followed by 2× SSC/0.1% NP40 at room temperature for 1 minute. The wash step was necessary to remove non-specific hybridization signals. Slides were then counterstained and mounted with 10 μl 4',6-diamidino-2-phenylindole (DAPI II, 125 ng/ml, Vysis).
For each hybridization experiment, 200 interphase cells were examined under oil immersion at 1000× magnification using the Nikon (model 80i) fluorescence microscope. The FISH signals were analyzed with fluorochrome-specific single band-pass filters for the BCR (SpectrumGreen signals) and ABL1 (SpectrumOrange signals). The BCR-ABL1 fusion signals were scored with a dual band-pass filter. For the tri-colour dual fusion system, cells were further examined using a single band-pass filter specific for the ASS1 (SpectrumAqua signals). Signal patterns in both interphase and metaphase were characterized using both D-FISH and tri-colour dual fusion FISH system. The Cytovision imaging workstation (Version 2.7) was used for image capture and processing.
This study was performed according to the regulation set by the Ethics Committee of Queen Elizabeth Hospital.
Interphase FISH is being used increasingly for the diagnosis and therapeutic monitoring of CML. Despite the simplicity and rapid turn-around-time of the test, inappropriate interpretation of signal pattern may compromise the sensitivity of the test . Technically, this can be due to poor hybridization signal or the presence of undesirable background. Moreover, the interpretation is sometimes difficult due to the inherent nature of signal integrity (e.g. split signals) and signal overlap. With the application of BCR-ABL1 D-FISH probe, the false positive rate due to signal overlap has been reduced to < 1% in comparison to the single fusion BCR-ABL1 probe .
Deletion of the ABL1 gene on der(9) has been shown to be a poor prognostic marker in CML [3, 4] although its effect can be overcome by the use of imatinib . Different types of submicroscopic deletion of the BCR and/or ABL1 have been well characterized with various BCR-ABL1 probe system [8, 9]. However, most studies have focused on the fusion signal pattern on interphase cells and few have applied the BCR-ABL1 + 9q34 tri-colour FISH probe system [1, 10]. In this study, we have used D-FISH and tri-colour dual fusion system to study both metaphase and interphase signal patterns. The parallel analysis of both FISH system on metaphase has not been reported previously. Our result provides the basic groundwork towards the better understanding of the various BCR-ABL1 deletions and the correct interpretation of interphase FISH signals.
The D-FISH system is adequate for the diagnosis and therapeutic monitoring of CML with the classical t(9;22) (1G1O2F pattern) (Figure 2A, upper panel) and even for cases with ABL1 or BCR deletion, because in the latter, the single genuine fusion can be readily differentiated from random signal overlap due to the 'extra' green or orange signal (Figure 2B–C, upper panel). In addition, the D-FISH gives very reliable and specific delineation of the different signal patterns in metaphases (Figure 2A–D, upper panel). It is, however, difficult to differentiate random signal overlap from genuine fusion in cases with reciprocal ABL1-BCR deletion which will have 1G1O1F signal pattern in positive cells when tested by D-FISH (Figure 2D, upper panel). This single fusion pattern is often not a problem when the diagnostic sample is tested because the abnormal signal pattern is present in most interphase cells . However, when interphase FISH is performed for disease monitoring, an atypical D-FISH result should be confirmed by the tri-colour dual fusion system. This is because the added aqua-labeled ASS1 probe consistently allows the discrimination of random signal overlap from genuine BCR-ABL1 fusion by the lack of aqua signal in the der(22) as the ASS1 is not involved in the t(9;22) and will remain in the der(9). The tri-colour dual fusion system is particularly useful in the study of reciprocal ABL1-BCR deletion where the signal pattern of 1G1O1F may sometimes be seen in a normal cell with random signal overlap. We have used the tri-colour dual fusion probe system to investigate the discrepant D-FISH and RQ-RTPCR result in a patient with reciprocal ABL1-BCR deletion. The tri-colour system did not show any fusion signal and the major molecular response was confirmed (Figure 3).
While the D-FISH system can reliably detect BCR-ABL1 gene fusions, it is sometimes impossible to differentiate variant BCR-ABL1 and to exclude random signal overlap. For cases with atypical fusion signals due to events such as deletion of the ABL1 and/or BCR, complex BCR-ABL1 rearrangement and supernumerary Philadelphia (Ph), tri-colour dual fusion system can be used to further confirm the presence of BCR-ABL1 gene fusion. Finally, the tri-color dual fusion system should be recommended for monitoring residual disease in CML patients with der(9) deletion due to the superior analytical sensitivity over D-FISH in this group of patients.
The authors thank Ms Helen Wong for the preparation of the images.
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