Characteristics of novel myeloid precursor cell line, PC-MDS, established from a bone marrow of the patient with therapy-related myelodysplastic syndrome

Abstract We report on characteristics of the first human cell line, PC-MDS, derived from a bone marrow of a patient with therapy-related myelodysplastic syndrome (t-MDS) who had no overt post-MDS leukemia. Classic cytology analyses, immunophenotyping, cytogenetic and molecular genetic procedures wer...

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Veröffentlicht in:Leukemia research 2007-08, Vol.31 (8), p.1097-1105
Hauptverfasser: Bogdanović, Gordana, Jurišić, Vladimir, Kraguljac, Nada, Mrdjanović, Jasminka, Jakimov, Dimitar, Krtolica, Koviljka, Krajnović, Milena, Magić, Zvonko, Stojiljković, Bratislav, Andrijević, Ljiljana, Srdić, Tatjana, Baltić, Mirjana, Popović, Stevan
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Sprache:eng
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Zusammenfassung:Abstract We report on characteristics of the first human cell line, PC-MDS, derived from a bone marrow of a patient with therapy-related myelodysplastic syndrome (t-MDS) who had no overt post-MDS leukemia. Classic cytology analyses, immunophenotyping, cytogenetic and molecular genetic procedures were used for characterization of the cell line. PC-MDS cells are positive for the expression of CD13, CD15, CD30, CD33, and CD45 antigen. Positive cytochemical staining and immunophenotype analyses indicated that PC-MDS cells have some characteristics of the early myeloid precursor cell. The karyotype analysis of PC-MDS cell line revealed various numerical and structural changes including those typically associated with t-MDS: del(5)(q13)[7], der(5)t(5;11)(p11;q11)[13], −7[6], del(7)(q31)[2], +20[3], −20[4]. Evaluation of methylation status in a promoter region of p15, p16 and MGMT genes showed biallelic hypermethylation pattern of 5′ promoter region only in MGMT gene. PC-MDS is the first t-MDS derived cell line, and based on its immunological, cytogenetic and molecular characterization could be a new tool in evaluation of complex biology of MDS and a model for methylation studies.
ISSN:0145-2126
1873-5835
DOI:10.1016/j.leukres.2007.01.012