Quantitative assessment of MLAA-34 expression in diagnosis and prognosis of acute monocytic leukemia.

Cancer Immunol Immunother

Department of Clinical Hematology, 2nd Affiliated Hospital, School of Medicine, Xi'an Jiaotong University, 157, 5th West Road, 710004, Xi'an, Shaanxi, People's Republic of China.

Published: April 2011

MLAA-34 is a newly identified monocytic leukemia-associated antigen. Previous data indicated that MLAA-34 might be a novel anti-apoptosis factor related closely to carcinogenesis or progression of acute monocytic leukemia. The over-expression of MLAA-34 is intuitively expected to be associated with unfavorable clinical features in acute myeloid leukemia. However, there have been no clinical studies about the prognostic relevance of MLAA-34 expression in human malignancies. This study was done to investigate the clinical relevance of the expression of MLAA-34 in de novo acute myeloid leukemia. In 126 patients with de novo acute myeloid leukemia, the level of MLAA-34 expression and protein expression ratio were determined by using quantitative reverse transcriptase-PCR and western blot, respectively. The results were analyzed with respect to the patients' clinical features and treatment outcomes. Both MLAA-34 expression rates and expression levels were found to be higher in patients with the French-American-British classification subtype M5, and the expression levels were also higher in patients with a leukocyte number of ≥ 20 × 10(9)/L and patients with extramedullary disease. In addition, MLAA-34 over-expression (≥ median expression) was associated with an unfavorable day 7 response to induction chemotherapy and also associated with a poor survival rate. In multivariate analysis, high MLAA-34 levels was independently associated with a poorer relapse-free survival and overall survival in AML patients. In conclusion, our data indicate that MLAA-34 may be used as a prognostic marker for treatment decision-making in acute monocytic leukemia through validation by further studies.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11028658PMC
http://dx.doi.org/10.1007/s00262-011-0969-7DOI Listing

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