Abstract | OBJECTIVE: To investigate the correlation of all exone mutation in MLAA-34 gene with chemotherapeutic efficacy for leukemia. METHODS: The expression level of MLAA-34 gene in 40 patients with AML-M5 and 5 healthy volunteers as control was detected by RT-PCR and its effect on chemotherapeutic efficacy were analyzed by RT-PCR; the effect of MLAA-34 gene mutation on overall survival (OS) and progression-free survival (PFS) of AML-M5 patients was analyzed by sequencing of all 12 exoues in MLAA-34 gene, the correlation between the mutation of prognostic genes important to leukemia and the mutation of MLAA-34 gene was explored. RESULTS: The expression level of MLAA-34 gene was significantly up-regulated as compared with that of healthy volunteers, moreover this up-regulation was related with a C59T SNP site located in second exon of MLAA-34 gene, meanswhile this SNP site is affinitive to the well-known mdecular markers of AML, inclinding Fms-like tyrosine kinase (FLT-3) and DNA methyltransferase-3A(DNAMT3A). The AML-M5 patients with high expression of MLAA-34 gene poorly responded to chemotherapy, the AML-M5 patients with MLAA-34 C59T mulation had even more high expression of MLAA-34 gene and significantly short OS and PFS in comparison with those of patients without C59T mutation. CONCLUSION: The C59T mutation in MLAA-34 gene is a high risk factor for recurrence of AML, and may be a cadidate target for treatment of AML.
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Authors | Bo Lei, Wang-Gang Zhang, Yin-Xia Chen, Ai-Li He, Xing-Mei Cao, Wan-Hong Zhao, Jian-Li Wang, Jie Liu, Xiao-Rong Ma, Yun Yang, Peng-Yu Zhang, Jing Luo, Xin Meng |
Journal | Zhongguo shi yan xue ye xue za zhi
(Zhongguo Shi Yan Xue Ye Xue Za Zhi)
Vol. 26
Issue 1
Pg. 97-104
(Feb 2018)
ISSN: 1009-2137 [Print] China |
PMID | 29397825
(Publication Type: Journal Article)
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Chemical References |
- Antigens, Neoplasm
- DNMT3A protein, human
- DNA Methyltransferase 3A
- fms-Like Tyrosine Kinase 3
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Topics |
- Antigens, Neoplasm
- DNA Methyltransferase 3A
- Exons
- Humans
- Leukemia, Monocytic, Acute
- Leukemia, Myeloid, Acute
- Mutation
- Prognosis
- fms-Like Tyrosine Kinase 3
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