Regulation of JAK2 by miR-135a: prognostic impact in classic Hodgkin lymphoma

被引:134
作者
Navarro, Alfons [1 ]
Diaz, Tania [1 ]
Martinez, Antonio [2 ]
Gaya, Anna
Pons, Aina [1 ]
Gel, Bernat [3 ]
Codony, Carles
Ferrer, Gerardo [4 ]
Martinez, Carmen
Montserrat, Emili
Monzo, Mariano [1 ]
机构
[1] Univ Barcelona, Sch Med, Human Anat Unit, Mol Oncol & Embryol Lab,IDIBAPS, E-08036 Barcelona, Spain
[2] Hosp Clin Barcelona, IDIBAPS, Pathol Lab, Hematopathol Sect, Barcelona, Spain
[3] Univ Politecn Cataluna, Software Dept, Barcelona, Spain
[4] Hosp Clin Barcelona, IDIBAPS, Lab Translat Hematol, Inst Hematol & Oncol, Barcelona, Spain
关键词
REED-STERNBERG CELLS; MYELOPROLIFERATIVE DISORDERS; TYROSINE KINASE; HEMATOLOGICAL MALIGNANCIES; SIGNAL-TRANSDUCTION; STAT PATHWAY; TUMOR; EXPRESSION; MICRORNAS; FREQUENT;
D O I
10.1182/blood-2009-02-204842
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The behavior of classic Hodgkin lymphoma (cHL) is determined by both the intrinsic features of the tumor cells and the characteristics of the microenvironment, making the analysis of entire lymph nodes an effective approach to understanding the disease. We examined the influence of our previously reported 25-microRNA signature for cHL on clinical outcome in 89 homogeneously treated cHL patients with a median follow-up of 80 months. Patients with low miR-135a expression had a higher probability of relapse (P=.04) and a shorter disease-free survival (P=.02). Functional analysis of cHL cell lines showed that mature miR-135a levels increased after pre-miR-135a transfection, causing apoptosis and decreased cell growth. Target analysis showed a direct regulation by miR-135a of JAK2, a cytoplasmic tyrosine kinase involved in a specific subset of cytokine receptor signaling pathways. miR-135-amediated JAK2 down-regulation led to decreased mRNA and protein levels of the antiapoptotic gene Bcl-xL, suggesting a role for Bcl-xL in miR-135a/JAK2-mediated apoptosis. Our findings confirm the critical role of miR-135a in the survival of cHL cells and in the prognosis of cHL patients, indicating that novel treatment approaches targeting miR-135a may potentially benefit these patients. (Blood. 2009; 114: 2945-2951)
引用
收藏
页码:2945 / 2951
页数:7
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