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Increased monocyte chemoattractant protein 1 (MCP-1/CCL-2) serum level in acute myeloid leukemia

In: NEOPLASMA, vol. 54, no. 4
G. Mazur - T. Wrobel - A. Butrym - K. Kapelko-Slowik - R. Poreba - K. Kuliczkowski
Detaily:
Rok, strany: 2007, 285 - 289
O článku:
Acute myeloid leukaemia (AML) is an aggressive malignancy with accumulation of blasts in bone marrow. Myeloblasts can entry into peripheral blood stream and secondary localize in extramedullary sites. The regulation of this process has not been clearly explained so far, but interactions between some chemokines and their specific receptors could be one of the mechanisms responsible for such kind of migration. Monocyte chemoattractant protein 1 (MCP-1/CCL2) is the chemokine which could be involved in this process. The aim of the study was to evaluate plasma level of CCL2 in patients with AML. Plasma samples from 65 adult patients with AML taken before chemotherapy and in complete remission were measured by enzyme linked immunoassay to evaluate CCL2 levels. Control group consisted of 15 healthy subjects. In AML patients mean baseline CCL2 level (± SEM – standard error of measurement) was significantly higher than in normal control: 365,26 ± 5,62 pg/ml vs 265,56 ± 5,48 pg/ml respectively (p<0.01). We demonstrate increased mean CCL2 plasma level in untreated patients with AML. Significantly lower plasma level of CCL2 was observed in patients with M4 and M5 AML subtypes according to FAB classification. In AML group chemotherapy did not reduce CCL2 plasma level. Key words: MCP-1/CCL2, acute myeloid leukaemia, chemokines
Ako citovať:
ISO 690:
Mazur, G., Wrobel, T., Butrym, A., Kapelko-Slowik, K., Poreba, R., Kuliczkowski, K. 2007. Increased monocyte chemoattractant protein 1 (MCP-1/CCL-2) serum level in acute myeloid leukemia. In NEOPLASMA, vol. 54, no.4, pp. 285-289. 0028-2685.

APA:
Mazur, G., Wrobel, T., Butrym, A., Kapelko-Slowik, K., Poreba, R., Kuliczkowski, K. (2007). Increased monocyte chemoattractant protein 1 (MCP-1/CCL-2) serum level in acute myeloid leukemia. NEOPLASMA, 54(4), 285-289. 0028-2685.