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HER2 and p95HER2 differentially regulate miRNA expression in MCF-7 breast cancer cells and downregulate MYB proteins through miR-221/222 and miR-503

Gorbatenko, Andrej (författare)
Icahn School of Medicine at Mount Sinai,University of Copenhagen
Søkilde, Rolf (författare)
Lund University,Lunds universitet,Cancer och icke-kodande RNA,Forskargrupper vid Lunds universitet,Cancer and non coding RNA,Lund University Research Groups
Sorensen, Ester E. (författare)
University of Copenhagen
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Newie, Inga (författare)
Lund University,Lunds universitet,Bröstcancer-genetik,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Breastcancer-genetics,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine
Persson, Helena (författare)
Lund University,Lunds universitet,Cancer och icke-kodande RNA,Forskargrupper vid Lunds universitet,Cancer and non coding RNA,Lund University Research Groups
Morancho, Beatriz (författare)
Spanish Center for Biomedical Research Network in Oncology (CIBERONC),Vall d'Hebron University Hospital
Arribas, Joaquin (författare)
Autonomous University of Barcelona,Spanish Center for Biomedical Research Network in Oncology (CIBERONC),Vall d'Hebron University Hospital,Catalan Institution for Research and Advanced Studies
Litman, Thomas (författare)
University of Copenhagen
Rovira, Carlos (författare)
Lund University,Lunds universitet,Cancer och icke-kodande RNA,Forskargrupper vid Lunds universitet,Cancer and non coding RNA,Lund University Research Groups
Pedersen, Stine Falsig (författare)
University of Copenhagen
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 (creator_code:org_t)
2019-03-04
2019
Engelska.
Ingår i: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322. ; 9:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The HER2 oncogene and its truncated form p95HER2 play central roles in breast cancer. Here, we show that although HER2 and p95HER2 generally elicit qualitatively similar changes in miRNA profile in MCF-7 breast cancer cells, a subset of changes are distinct and p95HER2 shifts the miRNA profile towards the basal breast cancer subtype. High-throughput miRNA profiling was carried out 15, 36 and 60 h after HER2 or p95HER2 expression and central hits validated by RT-qPCR. miRNAs strongly regulated by p95HER2 yet not by HER2, included miR-221, miR-222, miR-503, miR-29a, miR-149, miR-196 and miR-361. Estrogen receptor-α (ESR1) expression was essentially ablated by p95HER2 expression, in a manner recapitulated by miR-221/-222 mimics. c-Myb family transcription factors MYB and MYBL1, but not MYBL2, were downregulated by p95HER2 and by miR-503 or miR-221/-222 mimics. MYBL1 3′UTR inhibition by miR-221/222 was lost by deletion of a single putative miR-221/222 binding sites. p95HER2 expression, or knockdown of either MYB protein, elicited upregulation of tissue inhibitor of matrix metalloprotease-2 (TIMP2). miR-221/222 and -503 mimics increased, and TIMP2 knockdown decreased, cell migration and invasion. A similar pathway was operational in T47D- and SKBr-3 cells. This work reveals important differences between HER2- and p95HER2- mediated miRNA changes in breast cancer cells, provides novel mechanistic insight into regulation of MYB family transcription factors by p95HER2, and points to a role for a miR-221/222– MYB family–TIMP2 axis in regulation of motility in breast cancer cells.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

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