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MYCN-regulated miRNA-92 inhibits secretion of the tumor suppressor DICKKOPF-3 (DKK3) in neuroblastoma.

Haug, Bjørn Helge (author)
Henriksen, Jørn R (author)
Buechner, Jochen (author)
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Geerts, Dirk (author)
Tømte, Ellen (author)
Kogner, Per (author)
Karolinska Institutet
Martinsson, Tommy, 1956 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik,Institute of Biomedicine, Department of Medical and Clinical Genetics
Flægstad, Trond (author)
Sveinbjørnsson, Baldur (author)
Karolinska Institutet
Einvik, Christer (author)
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 (creator_code:org_t)
2011-05-13
2011
English.
In: Carcinogenesis. - : Oxford University Press (OUP). - 1460-2180 .- 0143-3334. ; 32:7, s. 1005-12
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The MYCN oncogene is frequently amplified in neuroblastoma. It is one of the most consistent markers of bad prognosis for this disease. Dickkopf-3 (DKK3) is a secreted protein of the DKK family of Wnt regulators. It functions as a tumor suppressor in a range of cancers, including neuroblastoma. MYCN was recently found to downregulate DKK3 mRNA. In this study, we show that MYCN knockdown in MYCN-amplified (MNA) neuroblastoma cell lines increases secretion of endogenous DKK3 to the culture media. MicroRNAs (miRNAs) are ∼20 nt long single-stranded RNA molecules that downregulate messenger RNAs by targeting the 3' untranslated region (3'UTR). Many miRNAs regulate genes involved in the pathogenesis of cancer and are extensively deregulated in different tumors. Using miRNA target prediction software, we found several MYCN-regulated miRNAs that could target the 3'UTR sequence of DKK3, including mir-92a, mir-92b and let-7e. Luciferase expression from a reporter vector containing the DKK3-3'UTR was decreased when this construct was cotransfected with mir-92a, mir-92b or let-7e in HEK293 cells. Mutation of the mir-92 seed sequence in the 3'UTR completely rescued the observed decrease in reporter expression when cotransfected with mir-92a and mir-92b. Antagomir and miRNA-mimic transfections in neuroblastoma cell lines confirmed that DKK3 secretion to the culture media is regulated by mir-92. Consistent with reports from other cancers, we found DKK3 to be expressed in the endothelium of primary neuroblastoma samples and to be absent in tumors with MYCN amplification. Our data demonstrate that MYCN-regulated miRNAs are able to modulate the expression of the tumor suppressor DKK3 in neuroblastoma.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)

Keyword

3' Untranslated Regions
Blood Vessels
metabolism
Cell Line
Tumor
DNA Methylation
Gene Knockdown Techniques
Genes
Tumor Suppressor
Humans
Immunohistochemistry
Intercellular Signaling Peptides and Proteins
genetics
metabolism
MicroRNAs
genetics
physiology
Neuroblastoma
blood supply
metabolism
pathology
Nuclear Proteins
genetics
physiology
Oncogene Proteins
genetics
physiology
Oncogenes
Polymerase Chain Reaction
Promoter Regions
Genetic
Reverse Transcriptase Polymerase Chain Reaction

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ref (subject category)
art (subject category)

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