An anti-apoptotic pattern correlates with multidrug resistance in acute myeloid leukemia patients: a comparative study of active caspase-3, cleaved PARPs, Bcl-2, Survivin and MDR1 gene

被引:19
作者
Guenova, Margarita L. [1 ]
Balatzenko, Gueorgui N. [2 ]
Nikolova, Vessela R. [1 ]
Spassov, Branimir V. [3 ]
Konstantinov, Spiro M. [4 ]
机构
[1] Natl Specialised Hosp Act Treatment Haematol Dis, Lab Haematopathol & Immunol, Blood Dis Diagnost Unit, Sofia 1756, Bulgaria
[2] Natl Specialised Hosp Act Treatment Haematol Dis, Blood Dis Diagnost Unit, Lab Cytogenet & Mol Biol, Sofia 1756, Bulgaria
[3] Natl Specialised Hosp Act Treatment Haematol Dis, Dept Clin Haematol, Sofia 1756, Bulgaria
[4] Med Univ Sofia, Lab Expt Chemotherapy, Sofia 1000, Bulgaria
关键词
Apoptosis; multidrug resistance; survivin; active caspase-3; bcl-2; cleaved PARP; MDR1; gene; acute myeloid leukemia; DRUG-RESISTANCE; POLY(ADP-RIBOSE) POLYMERASE; EXPRESSION; INHIBITOR; ACTIVATION; PROTEINS; CELLS; XIAP;
D O I
10.1179/102453309X12583347113690
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bone marrow samples of 17 acute myeloid leukemia (AML) patients were analyzed for apoptosis-related markers. The levels of active caspase-3 (aC-3), Bcl-2 and cleaved poly(ADP-ribose) polymerase (cPARP) were measured by flow cytometry and compared with survivin and MDR1 gene expression as defined by reverse transcriptase polymerase chain reaction (RT-PCR). The results showed heterogeneous patterns of intracellular levels of the studied proteins in AML patients: aC-3 (mean 34.6 +/- 52.5 U/ml), Bcl-2 (mean 3268.4 +/- 2055.2 U/ml), and cPARPs (mean 24.59 +/- 29.97 U/ml). Survivin and MDR1 genes were overexpressed in 9 and 10 patients, respectively. Patients with high levels of survivin mRNA showed significantly lower cPARPs (11.8 +/- 14.3 versus 53.9 +/- 31.9 U/ml P=0.005) and a tendency towards higher aC-3 (49.3 +/- 70.0 versus 18.1 +/- 9.9 U/ml), and MDR1 overexpression (7/9 patients versus 3/8 patients), as well as poorer therapeutic response and survival. Our data support the potential relevance of apoptosis-related markers in AML for further understanding the disease; however, the heterogeneity and complexity of molecular interactions warrants further prospective studies.
引用
收藏
页码:135 / 143
页数:9
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