Literature DB >> 22040965

Gene expression of helicase antigen in patients with acute and chronic myeloid leukemia.

Qin Chen1, Jiang Lin, Jun Qian, Dong-Ming Yao, Wei Qian, Yun Li, Hai-Yan Chai, Jing Yang, Cui-Zhu Wang, Ming Zhang, Gao-Fei Xiao.   

Abstract

The aim of this study was to investigate the expression status of the helicase antigen (HAGE) transcript and its clinical significance in patients with acute myeloid leukemia (AML) and chronic myeloid leukemia (CML). The expression of HAGE cDNA in bone marrow mononuclear cells from AML and CML patients was detected by using real-time quantitative PCR. The results indicated that overexpression of HAGE transcript (117.12% - 9842.70%, median 434.96%) was detected in 14.8% (11/74) AML patients. AML patients with HAGE cDNA expression were significantly older than those HAGE-negative patients (median 67 and 45 years, respectively, p = 0.001). HAGE cDNA expression was more frequently present among the patients with acute monoblastic leukemia (M(4) and M(5), 7 of 20, 35.0%), compared to the patients with acute non-monoblastic leukemia (M(1), M(2), M(3) and M(6), 4 of 54, 7.4%) (p = 0.007). 28.6% (8/28) cases with normal karyotypes showed HAGE cDNA overexpression, significantly higher than 7.5% (3 of 40) in those with chromosomal abnormalities (p = 0.041). Overexpression of HAGE transcript was found in 9 (34.6%) CML cases and more frequently observed at accelerated phase and blast crisis (4/4, 100%) than that at chronic phase (5/22, 22.7%) (p = 0.008). It is concluded that HAGE cDNA expression is relevant to specific subtypes of AML and to the progression of CML.

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Year:  2011        PMID: 22040965

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


  4 in total

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Authors:  Tanu Talwar; Venkatasubramanian Vidhyasagar; Jennifer Qing; Manhong Guo; Ahmad Kariem; Yi Lu; Ravi Shankar Singh; Kiven Erique Lukong; Yuliang Wu
Journal:  J Biol Chem       Date:  2017-05-03       Impact factor: 5.157

2.  HAGE (DDX43) is a biomarker for poor prognosis and a predictor of chemotherapy response in breast cancer.

Authors:  T M A Abdel-Fatah; S E B McArdle; C Johnson; P M Moseley; G R Ball; A G Pockley; I O Ellis; R C Rees; S Y T Chan
Journal:  Br J Cancer       Date:  2014-04-22       Impact factor: 7.640

3.  Arresting of miR-186 and releasing of H19 by DDX43 facilitate tumorigenesis and CML progression.

Authors:  J Lin; J-C Ma; J Yang; J-Y Yin; X-X Chen; H Guo; X-M Wen; T-J Zhang; W Qian; J Qian; Z-Q Deng
Journal:  Oncogene       Date:  2018-02-16       Impact factor: 9.867

4.  The KH domain facilitates the substrate specificity and unwinding processivity of DDX43 helicase.

Authors:  Manisha Yadav; Ravi Shankar Singh; Daniel Hogan; Venkatasubramanian Vidhyasagar; Shizhuo Yang; Ivy Yeuk Wah Chung; Anthony Kusalik; Oleg Y Dmitriev; Miroslaw Cygler; Yuliang Wu
Journal:  J Biol Chem       Date:  2020-11-23       Impact factor: 5.157

  4 in total

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