JANCUSKOVA, T, R PLACHY, Jiří ŠTIKA, L ZEMANKOVA, DW HARDEKOPF, T LIEHR, N KOSYAKOVA, R CMEJLA, L ZEJSKOVA, T KOZAK, P ZAK, A ZAVRELOVA, P HAVLIKOVA, M KARAS, A JUNGE, C RAMEL and S PEKOVA. A method to identify new molecular markers for assessing minimal residual disease in acute leukemia patients. Leukemia Research. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD, 2013, vol. 37, No 10, p. 1363-1373. ISSN 0145-2126. Available from: https://dx.doi.org/10.1016/j.leukres.2013.06.009.
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Basic information
Original name A method to identify new molecular markers for assessing minimal residual disease in acute leukemia patients
Authors JANCUSKOVA, T, R PLACHY, Jiří ŠTIKA, L ZEMANKOVA, DW HARDEKOPF, T LIEHR, N KOSYAKOVA, R CMEJLA, L ZEJSKOVA, T KOZAK, P ZAK, A ZAVRELOVA, P HAVLIKOVA, M KARAS, A JUNGE, C RAMEL and S PEKOVA.
Edition Leukemia Research, OXFORD, PERGAMON-ELSEVIER SCIENCE LTD, 2013, 0145-2126.
Other information
Original language English
Type of outcome Article in a journal
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 2.692
Doi http://dx.doi.org/10.1016/j.leukres.2013.06.009
UT WoS 000324099100031
Keywords in English Acute leukemia; Minimal residual disease; Cytogenetics; Chromosome microdissection; Next-generation sequencing; Personalized medicine
Tags International impact, Reviewed
Changed by Changed by: Mgr. Jiří Štika, Ph.D., učo 8741. Changed: 23/8/2018 14:25.
Abstract
Acute leukemias (AL) comprise a heterogeneous group of hematologic malignancies, and individual patient responses to treatment can be difficult to predict. Monitoring of minimal residual disease (MRD) is thus very important and holds great potential for improving treatment strategies. Common MRD targets include recurrent cytogenetic abnormalities and mutations in important hematological genes; unfortunately well-characterized targets are lacking in many AL patients. Here we demonstrate a technical approach for the identification and mapping of novel clone-specific chromosomal abnormalities down to the nucleotide level. We used molecular cytogenetics, chromosome microdissection, amplification of the microdissected material, and next-generation sequencing to develop PCR-based MRD assays based on unique breakpoint sequences. (C) 2013 Elsevier Ltd. All rights reserved.
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