Autor: |
Weber Axel, Taube Sylvia, zur Stadt Udo, Horstmann Martin, Krohn Knut, Bradtke Jutta, Teigler-Schlegel Andrea, Leiblein Sabine, Christiansen Holger |
Jazyk: |
angličtina |
Rok vydání: |
2012 |
Předmět: |
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Zdroj: |
Experimental Hematology & Oncology, Vol 1, Iss 1, p 33 (2012) |
Druh dokumentu: |
article |
ISSN: |
2162-3619 |
DOI: |
10.1186/2162-3619-1-33 |
Popis: |
Abstract The amplification of putative oncogenes is a common finding within the genome of various cancer types. Identification and further targeting of specific junction sites within the sequence of genomic amplicons (amplicon fusion sites, AFS) by PCR (AFS-PCR) is suitable for quantification of minimal residual disease (MRD). This approach has recently been developed and described for MYCN amplified neuroblastomas. To compare AFS-PCR directly to routinely used MRD diagnostic strategies, we mapped the amplified genomic regions (ampGR) of an iAMP21-amplicon in high resolution of a patient with acute lymphoblastic leukemia (ALL). Successfully, we established AFS-PCR covering junction sites between ampGR within the iAMP21-amplicon. Quantification of MRD by AFS-PCR was directly comparable to IgH/TCR based real time quantitative PCR and fluorescence activated cell sorting (FACS) analysis in consecutive bone marrow (BM) specimens. Our data give an additional proof of concept of AFS-PCR for quantification of MRD. The method could be taken into account for ALL patients with genomic amplifications as alternative MRD diagnostic, if no or qualitatively poor Ig/TCR-PCRs are available. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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