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Semi-quantitative study of calcitonin gene methylation in myelodyspastic syndrome

机译:降钙素基因甲基化在骨髓增生异常综合症中的半定量研究

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Conclusion: the results suggest that hyperme- thylation of CT gene occurs in early stage of leukemic transformation and CTMR might be a useful marker in predicting the transformation of MDS to AML. Objective To evaluate whether hypermethylation Of calcitonin (CT) gene could serve as a transforming signal of myelodysplastic syndrome (MDS) to leukemi- a. Methods: Bone marrow aspirates from 35 MDS Patients, including 25 refractory anemia (RA), 10 re- fractory anemia with excess of blasts (RAEB) or re- fractory anemia with excess of blasts in transfomation (RAEBt) and 7 cases of acute myeloid leukemia (AML) transformed form MDS, were studied on methylation rate in 5' end of CT gene by polymerase chain reaction (PCR) technique using methylation-sen- sitive endonuclease Hpa Ⅱ with external references of undigested DNA and Msp Ⅰ digested DNA and internal reference of 112 bp fragment containing codon 61 of N- ras oncogene.
机译:结论:结果表明,CT基因的过度甲基化发生在白血病转化的早期,CTMR可能是预测MDS向AML转化的有用标志。目的探讨降钙素(CT)基因的高甲基化是否可以作为骨髓增生异常综合征(MDS)向白血病的转化信号。方法:从35名MDS患者中抽取骨髓,包括25例难治性贫血(RA),10例难治性贫血伴胚泡过多(RAEB)或难治性贫血并伴胚泡过度转化(RAEBt)和7例急性髓样用甲基化敏感的核酸内切酶HpaⅡ,结合未消化的DNA和MspⅠ消化的DNA的内部参照,通过聚合酶链反应(PCR)技术研究了白血病(AML)从MDS转化为MDS的CT基因的甲基化率含有N-ras癌基因密码子61的112bp片段的参考。

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