Aberrant hnRNP K expression: All roads lead to cancer

Miguel Gallardo, Marisa J. Hornbaker, Xiaorui Zhang, Peter Hu, Carlos Bueso-Ramos, Sean M. Post

Research output: Contribution to journalReview articlepeer-review

73 Scopus citations

Abstract

ABSTRACT: The classification of a gene as an oncogene or a tumor suppressor has been a staple of cancer biology for decades. However, as we delve deeper into the biology of these genes, this simple classification has become increasingly difficult for some. In the case of heterogeneous nuclear ribonuclear protein K (hnRNP K), its role as a tumor suppressor has recently been described in acute myeloid leukemia and demonstrated in a haploinsufficient mouse model. In contrast, data from other clinical correlation studies suggest that hnRNP K may be more fittingly described as an oncogene, due to its increased levels in a variety of malignancies. hnRNP K is a multifunctional protein that can regulate both oncogenic and tumor suppressive pathways through a bevy of chromatin-, DNA-, RNA-, and protein-mediated activates, suggesting its aberrant expression may have broad-reaching cellular impacts. In this review, we highlight our current understanding of hnRNP K, with particular emphasis on its apparently dichotomous roles in tumorigenesis.

Original languageEnglish (US)
Pages (from-to)1552-1557
Number of pages6
JournalCell Cycle
Volume15
Issue number12
DOIs
StatePublished - Jun 17 2016

Keywords

  • 9q21.32
  • C/EBP
  • acute myeloid leukemia
  • c-Myc
  • haploinsufficiency
  • hnRNP K
  • mouse models
  • p21
  • p53

ASJC Scopus subject areas

  • Molecular Biology
  • Developmental Biology
  • Cell Biology

MD Anderson CCSG core facilities

  • Genetically Engineered Mouse Facility
  • Research Animal Support Facility

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