Literature DB >> 20030915

[Methylation status of JunB and CDH13 gene promoter in CD34(+)CD38(-) chronic myelogenous leukemia cells].

Xiao-Juan Wang1, Juan Li, Bing-Jie Fu, Lin-Lin Guo, Jia-Hua Zhang, Shi-Ang Huang.   

Abstract

Chronic myelogenous leukemia (CML) is a clonal myeloproliferative disease of transformed hematopoietic progenitor cells. The expressions of JunB and CDH13 (cadherin-13) gene as tumor suppressor gene were inactivated by promoter methylation in CML patients. This study was purposed to investigate the methylation difference of JunB and CDH13 gene promoter and the expression levels of JunB and CDH13 gene in CD34(+)CD38(-) cells in CML patients vs normal individuals. CD34(+)CD38(-) cells from 8 cases of CML and 5 normal individuals were selected by flow cytometry. The methylation status of JunB and CDH13 genes were detected by MS-PCR in selected CD34(+)CD38(-) cells. The expression levels of JunB and CDH13 gene was detected with real time polymerase chain reaction (RT-PCR). The results showed that no methylation of JunB and CDH13 gene was detected in CD34(+)CD38(-) cells of 5 normal individuals. Methylations of JunB and CDH13 promoter were found in 87.5% (7/8) and 50% (4/8) CML CD34(+)CD38(-) cells, percentages of which were significantly higher than those in normal individuals. The difference was statistically significant (p < 0.05). The relative expression levels of JunB and CDH13 mRNA in CD34(+)CD38(-) cells of CML patients were significantly lower than those in normal individuals (2(-DeltaDeltaCT) were 1/5.21 and 1/10.63 respectively). It is concluded that the high methylation of JunB and CDH13 gene promoter occurs in CD34(+)CD38(-) cells of CML patients, their mRNA expression level is significantly lower, thus the methylation of JunB and CDH13 gene promoter probably plays a role in the pathogenesis of CML and may have clinical significance in predicting prognosis of CML.

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Year:  2009        PMID: 20030915

Source DB:  PubMed          Journal:  Zhongguo Shi Yan Xue Ye Xue Za Zhi        ISSN: 1009-2137


  5 in total

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Journal:  Mol Clin Oncol       Date:  2016-07-12

2.  Aberrant DNA methylation at HOXA4 and HOXA5 genes are associated with resistance to imatinib mesylate among chronic myeloid leukemia patients.

Authors:  Marjanu Hikmah Elias; Husin Azlan; Sarina Sulong; Abdul Aziz Baba; Ravindran Ankathil
Journal:  Cancer Rep (Hoboken)       Date:  2018-07-27

3.  β-Catenin is required for intrinsic but not extrinsic BCR-ABL1 kinase-independent resistance to tyrosine kinase inhibitors in chronic myeloid leukemia.

Authors:  A M Eiring; J S Khorashad; D J Anderson; F Yu; H M Redwine; C C Mason; K R Reynolds; P M Clair; K C Gantz; T Y Zhang; A D Pomicter; I L Kraft; A D Bowler; K Johnson; M Mac Partlin; T O'Hare; M W Deininger
Journal:  Leukemia       Date:  2015-07-23       Impact factor: 11.528

Review 4.  The diagnostic value of DNA methylation in leukemia: a systematic review and meta-analysis.

Authors:  Danjie Jiang; Qingxiao Hong; Yusheng Shen; Yan Xu; Huangkai Zhu; Yirun Li; Chunjing Xu; Guifang Ouyang; Shiwei Duan
Journal:  PLoS One       Date:  2014-05-08       Impact factor: 3.240

5.  Aberrant DNA methylation of PTPRG as one possible mechanism of its under-expression in CML patients in the State of Qatar.

Authors:  Mohamed A Ismail; Muthanna Samara; Ali Al Sayab; Mohamed Alsharshani; Mohamed A Yassin; Govindarajulu Varadharaj; Marzia Vezzalini; Luisa Tomasello; Maria Monne; Hisham Morsi; M Walid Qoronfleh; Hatem Zayed; Richard Cook; Claudio Sorio; Helmout Modjtahedi; Nader I Al-Dewik
Journal:  Mol Genet Genomic Med       Date:  2020-07-23       Impact factor: 2.183

  5 in total

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