Hu Nan, Zhu Huan-ling, Liu Heng-wei, Zeng Chun-xue, Meng Wen-tong, Liu Ting
Hematology Department, West China Hospital, Sichuan University, Chengdu 610041, China.
Zhonghua Xue Ye Xue Za Zhi. 2009 Sep;30(9):596-600.
To explore the correlation between hOCT1 polymorphism and imatinib mesylate (IM) effectiveness in chronic myelogenous leukemia(CML) patients, and to provide for the clinical individual personalized therapy.
Fifty-three CML and 23 non-CML patients were enrolled in this study. Blood or bone marrow samples were collected. Amplification refractory mutation system (ARMS)-polymerase chain reaction was used to amplify the polymorphisms gene segment of hOCT1-P283L, R287G and M408V and their frequencies were statistically analysed. With clinical outcomes, the correlation between hOCT1 polymorphism and IM effectiveness in CML was analyzed.
(1) For 74 Han Chinese, the allele frequencies of hOCT1-P283L, R287G and M408V were 39.86%, 29.05% and 45.27%, respectively. (2) The genotypes of hOCT1-P283L, R287G and M408V in 2 Tibetan Chinese were CC, CC, AG and CC, CG, AG, respectively. (3) In the CML patients with IM optimal response, the frequencies of 283T and 287G allele were predominant (P<0.05). No significant difference was found in the frequency distribution of hOCT1-M408V genotype and allele among the 3 different response groups (P>0.05).
(1) Three single nucleotide polymorphisms (cSNP) P283L, R287G and M408V were found in the hOCT1 gene from 76 Chinese. (2) hOCT1 gene polymorphism is associated with the long-term molecular response of CML patients received IM therapy, indicating that the polymorphisms of hOCT1-283T, 287G may be good predictors for IM response. (3) There is no correlation between the polymorphisms of hOCT1-P283L, R287G, M408V and secondary IM resistance in CML patients.
探讨慢性髓性白血病(CML)患者中hOCT1基因多态性与甲磺酸伊马替尼(IM)疗效的相关性,为临床个体化治疗提供依据。
本研究纳入53例CML患者和23例非CML患者。采集血液或骨髓样本。采用扩增阻滞突变系统(ARMS)-聚合酶链反应扩增hOCT1-P283L、R287G和M408V的多态性基因片段,并对其频率进行统计学分析。结合临床结局,分析CML患者中hOCT1基因多态性与IM疗效的相关性。
(1)74名汉族人中,hOCT1-P283L、R287G和M408V的等位基因频率分别为39.86%、29.05%和45.27%。(2)2名藏族人中,hOCT1-P283L、R287G和M408V的基因型分别为CC、CC、AG和CC、CG、AG。(3)在IM治疗反应最佳的CML患者中,283T和287G等位基因频率占主导(P<0.05)。3个不同反应组中hOCT1-M408V基因型和等位基因频率分布无显著差异(P>0.05)。
(1)在76名中国人的hOCT1基因中发现了3个单核苷酸多态性(cSNP)P283L、R287G和M408V。(2)hOCT1基因多态性与接受IM治疗的CML患者的长期分子反应相关,表明hOCT1-283T、287G的多态性可能是IM反应的良好预测指标。(3)CML患者中hOCT1-P283L、R287G、M408V的多态性与IM继发性耐药无关。