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Relationship between RAD51-G135C and XRCC3-C241T Single Nucleotide Polymorphisms and Onset of Acute Myeloid Leukemia / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 605-611, 2015.
Article in Chinese | WPRIM | ID: wpr-357306
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the relationship between RAD51-G135C and XRCC3-C241T single nucleotide polymorphisms and onset of acute myeloid leukemia (AML).</p><p><b>METHODS</b>The study was performed in 2 groups AML patient group and normal person group as control group. Genomic DNA was extracted from peripheral blood cells of 545 AML patients and 1 034 normal persons. Genotypes of RAD51-G135C and XRCC3-C241T were analyzed by TaqMan probe technology and the ralatienship between RAD51-G135C/XRCC3-C241T polymorphisms and onset of acute myeloid leukemia was investigated.</p><p><b>RESULTS</b>Compared with the control group, RAD51-G135C homozygous mutant (CC) could significantly increase the risk of AML patients (OR=3.07), and there was no statistical relationship between heterozygous mutant (GC) of RAD51-G135C and onset of AML. There was no statistical relationship between homozygous mutant (TT) of XRCC3-C241T and onset of AML, and the XRCC3-C241T heterozygous mutation type (CT) increased the risk of AML patients (OR=0.66).</p><p><b>CONCLUSION</b>RAD51-G135C homozygous mutant and XRCC3-C241T heterozygous mutation significantly increase the risk of the AML onset, which can provide more predictive value for incidence of AML.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Leukemia, Myeloid, Acute / Polymorphism, Single Nucleotide / DNA-Binding Proteins / Rad51 Recombinase / Heterozygote / Homozygote Type of study: Prognostic study Limits: Humans Language: Chinese Journal: Journal of Experimental Hematology Year: 2015 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Leukemia, Myeloid, Acute / Polymorphism, Single Nucleotide / DNA-Binding Proteins / Rad51 Recombinase / Heterozygote / Homozygote Type of study: Prognostic study Limits: Humans Language: Chinese Journal: Journal of Experimental Hematology Year: 2015 Type: Article