MiR‐137 functions as a tumor suppressor in neuroblastoma by downregulating KDM1A. Issue 5 (7th March 2013)

• Record Type: Journal Article
• Authors: Althoff, Kristina; Beckers, Anneleen; Odersky, Andrea; Mestdagh, Pieter; Köster, Johannes; Bray, Isabella M.; Bryan, Kenneth; Vandesompele, Jo; Speleman, Frank; Stallings, Raymond L.; Schramm, Alexander; Eggert, Angelika; Sprüssel, Annika; Schulte, Johannes H.
• Is Part Of: International journal of cancer. Volume 133:Issue 5(2013:Sep. 01)
• Page Start: 1064
• Page End: 1073
• Publication Date: 2013-03-07
• Subjects: Cancer -- Periodicals; Cancer -- Prevention -- Periodicals; 616.994
• DOI: 10.1002/ijc.28091
• Languages: English
• ISSNs: 0020-7136

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Neuroblastoma is the most common extracranial solid tumor of childhood, and accounts for ∼15% of all childhood cancer deaths. The histone demethylase, lysine‐specific demethylase 1 (KDM1A, previously known as LSD1), is strongly expressed in neuroblastomas, and overexpression correlates with poor patient prognosis. Inducing differentiation in neuroblastoma cells has previously been shown to down regulate KDM1A, and siRNA‐mediated KDM1A knockdown inhibited neuroblastoma cell viability. The microRNA, miR‐137, has been reported to be downregulated in several human cancers, and KDM1A mRNA was reported as a putative target of miR‐137 in colon cancer. We hypothesized that miR‐137 might have a tumor‐suppressive role in neuroblastoma mediated via downregulation of KDM1A. Indeed, low levels of miR‐137 expression in primary neuroblastomas correlated with poor patient prognosis. Re‐expressing miR‐137 in neuroblastoma cell lines increased apoptosis and decreased cell viability and proliferation. <italic>KDM1A</italic> mRNA was repressed by miR‐137 in neuroblastoma cells, and was validated as a direct target of miR‐137 using reporter assays in SHEP and HEK293 cells. Furthermore, siRNA‐mediated KDM1A knockdown phenocopied the miR‐137 re‐expression phenotype in neuroblastoma cells. We conclude that miR‐137 directly targets <italic>KDM1A</italic> mRNA in neuroblastoma cells, and activates cell properties consistent with tumor suppression. Therapeutic strategies to re‐express miR‐137 in neuroblastomas could be useful to reduce tumor aggressiveness.</p> </abstract>