MicroRNA-17∼92 plays a causative role in lymphomagenesis by coordinating multiple oncogenic pathways

Hyun Yong Jin, Hiroyo Oda, Maoyi Lai, Rebecca L. Skalsky, Kelly Bethel, Jovan Shepherd, Seung Goo Kang, Wen Hsien Liu, Mohsen Sabouri-Ghomi, Bryan R. Cullen, Klaus Rajewsky, Changchun Xiao

Research output: Contribution to journalArticlepeer-review

122 Scopus citations


MicroRNAs (miRNAs) have been broadly implicated in cancer, but their exact function and mechanism in carcinogenesis remain poorly understood. Elevated miR-17∼92 expression is frequently found in human cancers, mainly due to gene amplification and Myc-mediated transcriptional upregulation. Here we show that B cell-specific miR-17∼92 transgenic mice developed lymphomas with high penetrance and that, conversely, Myc-driven lymphomagenesis stringently requires two intact alleles of miR-17∼92. We experimentally identified miR-17∼92 target genes by PAR-CLIP and validated select target genes in miR-17∼92 transgenic mice. These analyses demonstrate that miR-17∼92 drives lymphomagenesis by suppressing the expression of multiple negative regulators of the PI3K and NFκB pathways and by inhibiting the mitochondrial apoptosis pathway. Accordingly, miR-17∼92-driven lymphoma cells exhibited constitutive activation of the PI3K and NFκB pathways and chemical inhibition of either pathway reduced tumour size and prolonged the survival of lymphoma-bearing mice. These findings establish miR-17∼92 as a powerful cancer driver that coordinates the activation of multiple oncogenic pathways, and demonstrate for the first time that chemical inhibition of miRNA downstream pathways has therapeutic value in treating cancers caused by miRNA dysregulation.

Original languageEnglish (US)
Pages (from-to)2377-2391
Number of pages15
JournalEMBO Journal
Issue number17
StatePublished - Aug 28 2013
Externally publishedYes


  • NFκB
  • PI3K
  • lymphoma
  • miR-17∼92

ASJC Scopus subject areas

  • General Neuroscience
  • Molecular Biology
  • General Biochemistry, Genetics and Molecular Biology
  • General Immunology and Microbiology


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