4.7 Article

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

Journal

BLOOD
Volume 114, Issue 14, Pages 2945-2951

Publisher

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2009-02-204842

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Funding

  1. Spanish Ministry of Public Health [FISS-PI060087, PI080095]
  2. School of Medicine of the University of Barcelona
  3. Farreras-Valenti Foundation
  4. Agencia de Gestio D'Ajuts Universitaris I de Recerca (AGAUR)
  5. Generalitat de Catalunya
  6. Fondo Social Europeo

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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)

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