Evidence map›Paper›PMID 30709367›Full record

ArticleBreast cancer research : BCR2019

MiR-1287-5p inhibits triple negative breast cancer growth by interaction with phosphoinositide 3-kinase CB, thereby sensitizing cells for PI3Kinase inhibitors.

Daniela Schwarzenbacher, Christiane Klec, Barbara Pasculli, Stefanie Cerk, Beate Rinner, Michael Karbiener, Cristina Ivan, Raffaela Barbano, Hui Ling, Annika Wulf-Goldenberg and 10 more

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

  1. Pooled it
  2. METTL3-dependent mJournal of translational medicine · 2026
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  9. Article
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  11. Article
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  14. The functional role of circular RNAs in the pathogenesis of retinoblastoma: a new potential biomarker and therapeutic target?Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  15. Article
  16. Review
  17. Role of circular RNAs in retinoblastoma.Functional & integrative genomics · 2022
    Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 4 institutions in 4 countries.

Daniela SchwarzenbacherDivision of Oncology, Department of Internal Medicine, Medical University of Graz (MUG), Graz, Austria.
Christiane KlecDivision of Oncology, Department of Internal Medicine, Medical University of Graz (MUG), Graz, Austria.
Barbara PasculliFondazione IRCCS Casa Sollievo della Sofferenza Laboratorio di Oncologia, San Giovanni Rotundo, FG, Italy.
Stefanie CerkDivision of Oncology, Department of Internal Medicine, Medical University of Graz (MUG), Graz, Austria.
Beate RinnerBiomedical Research, Medical University of Graz, Graz, Austria.
Michael KarbienerDepartment of Phoniatrics, ENT University Hospital, Medical University of Graz, Graz, Austria.
Cristina IvanDepartment of Experimental Therapeutics -- Unit 1950, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Raffaela BarbanoFondazione IRCCS Casa Sollievo della Sofferenza Laboratorio di Oncologia, San Giovanni Rotundo, FG, Italy.
Hui LingDepartment of Experimental Therapeutics -- Unit 1950, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Annika Wulf-GoldenbergExperimental Pharmacology & Oncology GmbH, EPO, Berlin, Germany.
Stefanie StanzerDivision of Oncology, Department of Internal Medicine, Medical University of Graz (MUG), Graz, Austria.
Gabriel RinnerthalerIIIrd Medical Department with Hematology and Medical Oncology, Hemostaseology, Rheumatology and Infectious Diseases, Oncologic Center, Paracelsus Medical University, Salzburg, Austria.
Herbert StoegerDivision of Oncology, Department of Internal Medicine, Medical University of Graz (MUG), Graz, Austria.
Thomas BauernhoferDivision of Oncology, Department of Internal Medicine, Medical University of Graz (MUG), Graz, Austria.
Johannes HaybaeckInstitute of Pathology, Medical University of Graz, Graz, Austria.
Gerald HoeflerInstitute of Pathology, Medical University of Graz, Graz, Austria.
Stephan Wenzel JahnInstitute of Pathology, Medical University of Graz, Graz, Austria.
Paola ParrellaFondazione IRCCS Casa Sollievo della Sofferenza Laboratorio di Oncologia, San Giovanni Rotundo, FG, Italy.
George Adrian CalinDepartment of Experimental Therapeutics -- Unit 1950, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Martin PichlerDivision of Oncology, Department of Internal Medicine, Medical University of Graz (MUG), Graz, Austria. mart.pichler@gmx.net.
Medical University of Graz · ATThe University of Texas MD Anderson Cancer Center · USCasa Sollievo della Sofferenza · ITParacelsus Medical University · AT

Funding

Novel extra cellular RNA-based combinatorial RNA inhibition therapyUH3TR000943 · NCATS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CALIN, GEORGE A., LOPEZ-BERESTEIN, GABRIEL · 2015 to 2017
$3.2M
Protein-coding and non-coding RNA biomarkers for early detection of CLLR01CA182905 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ABRUZZO, LYNNE V., CALIN, GEORGE A. · 2014 to 2018
$2.9M
NCATS NIH HHS UH3 TR000943NCATS NIH HHS UH3TR00943-01NCI NIH HHS R01 CA182905NCI NIH HHS R01 CA182905-01
6 · The paper itself

Abstract

backgroundNon-coding RNAs and especially microRNAs have been discovered to act as master regulators of cancer initiation and progression. The aim of our study was to discover and characterize the function of yet functionally uncharacterized microRNAs in human breast carcinogenesis.

methodsIn an unbiased approach, we utilized an established model system for breast cancer (BC) stem cell formation ("mammosphere assay") to identify whole miRNome alterations in breast carcinogenesis. Clinical samples of BC patients were used to evaluate the human relevance of the newly identified miRNA candidates. One promising candidate, miR-1287-5p, was further explored on its impact on several hallmarks of cancer. The molecular mode of action was characterized by whole transcriptome analysis, in silico prediction tools, miRNA-interaction assays, pheno-copy assays, and drug sensitivity assays.

resultsAmong several other microRNAs, miR-1287-5p was significantly downregulated in mammospheres and human BC tissue compared to normal breast tissue (p < 0.0001). Low expression levels were significantly associated with poor prognosis in BC patients. MiR-1287-5p significantly decreased cellular growth, cells in S phase of cell cycle, anchorage-independent growth, and tumor formation in vivo. In addition, we identified PIK3CB as a direct molecular interactor of miR-1287-5p and a novel prognostic factor in BC. Finally, PI3Kinase pathway chemical inhibitors combined with miR-1287-5p mimic increased the pharmacological growth inhibitory potential in triple negative BC cells.

conclusionOur data identified for the first time the involvement of miR-1287-5p in human BC and suggest a potential for therapeutic interventions in difficult to treat triple negative BC.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsBreastCarcinogenesisCell Line, TumorCell ProliferationClass I Phosphatidylinositol 3-KinasesDown-RegulationFemaleGene Expression ProfilingHEK293 CellsHumansMiceMice, NudeMicroRNAsMiddle AgedClass I Phosphatidylinositol 3-KinasesMicroRNAsMIRN1287 microRNA, humanPIK3CB protein, humanBreast cancermicroRNAsNon-coding RNA

Identifiers

PMID30709367
PMCPMC6359814
OpenAlexW2920071715

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.