Evidence map›Paper›PMID 29568059›Full record

ArticleCell death and differentiation2018

Cell-autonomous and cell non-autonomous downregulation of tumor suppressor DAB2IP by microRNA-149-3p promotes aggressiveness of cancer cells.

Arianna Bellazzo, Giulio Di Minin, Elena Valentino, Daria Sicari, Denis Torre, Luigi Marchionni, Federica Serpi, Michael B Stadler, Daniela Taverna, Gaia Zuccolotto and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell death and differentiation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.6field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 41 citations in OpenAlex.

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  4. Computational and structural biotechnology journal · 2024
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  19. Oncogenic and tumor-suppressive microRNAs in prostate cancer.Current opinion in endocrine and metabolic research · 2020
    Article
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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

19 authors at 11 institutions in 4 countries.

Arianna BellazzoNational Laboratory CIB (LNCIB), AREA Science Park, 34149, Trieste, Italy.
Giulio Di MininInstitute of Molecular Health Sciences, Swiss Federal Institute of Technology (ETH) Hönggerberg, 8093, Zurich, Switzerland.
Elena ValentinoNational Laboratory CIB (LNCIB), AREA Science Park, 34149, Trieste, Italy.
Daria SicariNational Laboratory CIB (LNCIB), AREA Science Park, 34149, Trieste, Italy.
Denis TorreDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, BD2K-LINCS DCIC, Mount Sinai Center for Bioinformatics, New York, NY, 10029, USA.
Luigi MarchionniDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD, 21205, USA.
Federica SerpiNational Laboratory CIB (LNCIB), AREA Science Park, 34149, Trieste, Italy.
Michael B StadlerFriedrich Miescher Institute for Biomedical Research, Switzerland and Swiss Institute of Bioinformatics, 4058, Basel, Switzerland.ORCID http://orcid.org/0000-0002-2269-4934
Daniela TavernaDepartment of Molecular Biotechnology and Health Sciences, University of Torino, 10126, Torino, Italy.
Gaia ZuccolottoDepartment of Surgery Oncology and Gastroenterology, University of Padova, 35128, Padova, Italy.
Isabella Monia MontagnerIstituto Oncologico Veneto IOV-IRCCS, 35128, Padova, Italy.
Antonio RosatoDepartment of Surgery Oncology and Gastroenterology, University of Padova, 35128, Padova, Italy.
Federica TononDepartment of Medical Surgical and Health Sciences, University of Trieste, 34149, Trieste, Italy.
Cristina ZennaroDepartment of Medical Surgical and Health Sciences, University of Trieste, 34149, Trieste, Italy.ORCID http://orcid.org/0000-0003-4755-1064
Chiara AgostinisInstitute for Maternal and Child Health, IRCCS Burlo Garofolo, 34137, Trieste, Italy.
Roberta BullaDepartment of Life Sciences, University of Trieste, 34127, Trieste, Italy.
Miguel ManoCenter for Neuroscience and Cell Biology (CNC), University of Coimbra, 3004-504, Coimbra, Portugal.
Giannino Del SalNational Laboratory CIB (LNCIB), AREA Science Park, 34149, Trieste, Italy. delsal@lncib.it.
Licio CollavinNational Laboratory CIB (LNCIB), AREA Science Park, 34149, Trieste, Italy. collavin@lncib.it.ORCID http://orcid.org/0000-0001-6815-5381
University of Trieste · ITAREA Science Park · ITUniversity of Padua · ITÉcole Polytechnique Fédérale de Lausanne · CHIcahn School of Medicine at Mount Sinai · USIRCCS Materno Infantile Burlo Garofolo · ITIstituto Oncologico Veneto · ITJohns Hopkins University · USSIB Swiss Institute of Bioinformatics · CHUniversity of Coimbra · PTUniversity of Turin · IT

Funding

Hardwiring Mechanism into Predicting Cancer Phenotypes by Computational LearningR01CA200859 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI MARCHIONNI, LUIGI · 2016 to 2020
$1.9M
NCI NIH HHS R01 CA200859
6 · The paper itself

Abstract

The tumor suppressor DAB2IP contributes to modulate the network of information established between cancer cells and tumor microenvironment. Epigenetic and post-transcriptional inactivation of this protein is commonly observed in multiple human malignancies, and can potentially favor progression of tumors driven by a variety of genetic mutations. Performing a high-throughput screening of a large collection of human microRNA mimics, we identified miR-149-3p as a negative post-transcriptional modulator of DAB2IP. By efficiently downregulating DAB2IP, this miRNA enhances cancer cell motility and invasiveness, facilitating activation of NF-kB signaling and promoting expression of pro-inflammatory and pro-angiogenic factors. In addition, we found that miR-149-3p secreted by prostate cancer cells induces DAB2IP downregulation in recipient vascular endothelial cells, stimulating their proliferation and motility, thus potentially remodeling the tumor microenvironment. Finally, we found that inhibition of endogenous miR-149-3p restores DAB2IP activity and efficiently reduces tumor growth and dissemination of malignant cells. These observations suggest that miR-149-3p can promote cancer progression via coordinated inhibition of DAB2IP in tumor cells and in stromal cells.

Indexed as

Signal TransductionTumor MicroenvironmentAnimalsHCT116 CellsHeLa CellsHep G2 CellsHumansHuman Umbilical Vein Endothelial CellsMaleMicroRNAsNeoplasm ProteinsPC-3 CellsProstatic Neoplasmsras GTPase-Activating ProteinsRNA, NeoplasmZebrafishDAB2IP protein, humanMicroRNAsMIRN149 microRNA, humanNeoplasm Proteinsras GTPase-Activating ProteinsRNA, Neoplasm

Identifiers

PMID29568059
PMCPMC6030048
OpenAlexW2791854995

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.