Literature DB >> 21240483

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

Jianqiang Zhao1, Aili He, Wanggang Zhang, Xin Meng, Liufang Gu.   

Abstract

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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Year:  2011        PMID: 21240483     DOI: 10.1007/s00262-011-0969-7

Source DB:  PubMed          Journal:  Cancer Immunol Immunother        ISSN: 0340-7004            Impact factor:   6.968


  7 in total

1.  Prediction and identification of HLA-A*0201-restricted epitopes from leukemia-associated protein MLAA-22 which elicit cytotoxic T lymphocytes.

Authors:  Jing Li; Ju Bai; Liufang Gu; Aili He; Jin Wang; Jianli Wang; Pengyu Zhang; Wanggang Zhang
Journal:  Med Oncol       Date:  2014-10-30       Impact factor: 3.064

2.  The anti-apoptosis effect of MLAA-34 in leukemia and the β-catenin/T cell factor 4 protein pathway.

Authors:  Lu Qian; Wanggang Zhang; Pengyu Zhang; Bo Lei; Xiu Wang; Man Wang; Ju Bai; Aili He
Journal:  Am J Transl Res       Date:  2015-11-15       Impact factor: 4.060

3.  Serum peptidome based biomarkers searching for monitoring minimal residual disease in adult acute lymphocytic leukemia.

Authors:  Ju Bai; Aili He; Chen Huang; Juan Yang; Wanggang Zhang; Jianli Wang; Yun Yang; Pengyu Zhang; Yang Zhang; Fuling Zhou
Journal:  Proteome Sci       Date:  2014-09-16       Impact factor: 2.480

4.  Bioinformatic prediction and functional characterization of human KIAA0100 gene.

Authors:  He Cui; Xi Lan; Shemin Lu; Fujun Zhang; Wanggang Zhang
Journal:  J Pharm Anal       Date:  2016-11-02

5.  Prokaryotic expression of MLAA-34 and generation of a novel human ScFv against MLAA-34 by phage display technology.

Authors:  Yang Zhang; Pengyu Zhang; Aili He; Yun Yang; Jianli Wang; Hui Zhang; Wanggang Zhang
Journal:  Oncotarget       Date:  2017-06-13

6.  C59T mutation in exon 2 of monocytic leukemia-associated antigen-34 gene indicates a high risk of recurrence of acute myeloid leukemia.

Authors:  Bo Lei; Yinxia Chen; Aili He; Jing Luo; Pengyu Zhang; Fuling Zhou; Jie Liu; Xin Meng; Jing Wang; Wanggang Zhang
Journal:  Oncol Lett       Date:  2017-05-02       Impact factor: 2.967

7.  Leukemia-associated gene MLAA-34 reduces arsenic trioxide-induced apoptosis in HeLa cells via activation of the Wnt/β-catenin signaling pathway.

Authors:  Pengyu Zhang; Xuan Zhao; Wenjuan Zhang; Aili He; Bo Lei; Wanggang Zhang; Yinxia Chen
Journal:  PLoS One       Date:  2017-10-23       Impact factor: 3.240

  7 in total

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