miR-26a and miR-214 down-regulate expression of the PTEN gene in chronic lymphocytic leukemia, but not PTEN mutation or promoter methylation

被引:42
|
作者
Zou, Zhi-Jian [1 ,2 ]
Fan, Lei [1 ]
Wang, Li [1 ]
Xu, Ji [1 ]
Zhang, Run [1 ]
Tian, Tian [1 ]
Li, Jian-Yong [1 ]
Xu, Wei [1 ]
机构
[1] Nanjing Med Univ, Jiangsu Prov Hosp, Affiliated Hosp 1, Dept Hematol, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Wuxi People Hosp, Dept Hematol, Wuxi, Peoples R China
基金
中国国家自然科学基金;
关键词
chronic lymphocytic leukemia; PTEN; mutation; microRNA; ACUTE LYMPHOBLASTIC-LEUKEMIA; HIGH-FREQUENCY; MICRORNA; CANCER; AKT; PATHOGENESIS; INHIBITION; RESISTANCE; PROGNOSIS; APOPTOSIS;
D O I
10.18632/oncotarget.2626
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We previous found the expression level of PTEN was low in the chronic lymphocytic leukemia (CLL) patients. To assess the pathogenic contribution of the low expression of PTEN, we determined PTEN-regulating miRNA interference, PTEN promoter methylation and PTEN gene mutation condition in CLL. One hundred and fifty-four previously untreated CLL patients and 200 cases of healthy controls were sequenced in exons 5-9 of PTEN. None of single nucleotide polymorphism site or mutation was detected in the coding sequences of those exons. Methylation of PTEN promoter was found in one (1.33%) of the 75 patients with CLL, but none of the 25 age-matched control subjects. We found that PTEN was a potential target of miR-26a and miR-214, which had been confirmed following dual-luciferase reporter assays, reverse transcription polymerase chain reaction and Western blotting. High expression of miR-26a was associated with advanced Binet stage (P=0.012), p53 aberrations (P=0.014) and inferior time to first treatment (P=0.038), and high expression of miR-214 was only associated with p53 aberrations (P=0.041). Inhibition of miR-26a or miR-214 could induce more apoptosis in primary cultured CLL cells. These findings support miR-26a and miR-214 down-regulate expression of PTEN in CLL, but not PTEN mutation or promoter methylation.
引用
收藏
页码:1276 / 1285
页数:10
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