Evidence map›Paper›PMID 35163219›Full record

ArticleInternational journal of molecular sciences2022

Exosomal miRNAs from Prostate Cancer Impair Osteoblast Function in Mice.

Giulia Furesi, Antonio Miguel de Jesus Domingues, Dimitra Alexopoulou, Andreas Dahl, Matthias Hackl, Johannes R Schmidt, Stefan Kalkhof, Thomas Kurth, Hanna Taipaleenmäki, Stefanie Conrad and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 34 citations in OpenAlex.

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  18. Secreted microRNAs in bone metastasis.Journal of bone and mineral metabolism · 2023
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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

13 authors at 7 institutions in 1 country.

Giulia FuresiDepartment of Medicine III & Center for Healthy Aging, Technical University of Dresden, 01307 Dresden, Germany.ORCID 0000-0002-4542-1955
Antonio Miguel de Jesus DominguesMax Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.ORCID 0000-0002-1803-1863
Dimitra AlexopoulouDRESDEN-Concept Genome Center, DFG NGS Competence Center, c/o Center for Molecular and Cellular Bioengineering (CMCB), Technical University of Dresden, 01307 Dresden, Germany.ORCID 0000-0002-3715-1756
Andreas DahlDRESDEN-Concept Genome Center, DFG NGS Competence Center, c/o Center for Molecular and Cellular Bioengineering (CMCB), Technical University of Dresden, 01307 Dresden, Germany.ORCID 0000-0002-2668-8371
Matthias HacklTAmiRNA GmbH, 1110 Vienna, Austria.
Johannes R SchmidtDepartment of Preclinical Development and Validation, Fraunhofer Institute for Cell Therapy and Immunology IZI, 04103 Leipzig, Germany.ORCID 0000-0002-2026-9715
Stefan KalkhofDepartment of Preclinical Development and Validation, Fraunhofer Institute for Cell Therapy and Immunology IZI, 04103 Leipzig, Germany.ORCID 0000-0001-6121-7105
Thomas KurthCenter for Molecular and Cellular Bioengineering (CMCB), Technology Platform, EM and Histology Facility, TU Dresden, 01307 Dresden, Germany.ORCID 0000-0001-5624-1717
Hanna TaipaleenmäkiInstitute of Musculoskeletal Medicine (IMM), Musculoskeletal University Center Munich (MUM), University Hospital, LMU Munich, 82152 Planegg-Martinsried, Germany.ORCID 0000-0002-8254-9333
Stefanie ConradDepartment of Medicine III & Center for Healthy Aging, Technical University of Dresden, 01307 Dresden, Germany.
Christine HofbauerNational Center for Tumor Diseases, Technical University of Dresden, 01307 Dresden, Germany.
Martina RaunerDepartment of Medicine III & Center for Healthy Aging, Technical University of Dresden, 01307 Dresden, Germany.
Lorenz C HofbauerDepartment of Medicine III & Center for Healthy Aging, Technical University of Dresden, 01307 Dresden, Germany.
Technische Universität Dresden · DECenter for Systems Biology Dresden · DECoburg University of Applied Sciences · DEFraunhofer Institute for Cell Therapy and Immunology · DEMax Planck Institute of Molecular Cell Biology and Genetics · DENational Center for Tumor Diseases · DEUniversität Hamburg · DE

Funding

BMBF 01ZX1910BDeutsche Forschungsgemeinschaft uBone SPP2084Emmy Noether Programme TA1154/1-1Emmy Noether Programme TA1154/1-2
6 · The paper itself

Abstract

Prostate cancer (PCa) is the most frequent malignancy in older men with a high propensity for bone metastases. Characteristically, PCa causes osteosclerotic lesions as a result of disrupted bone remodeling. Extracellular vesicles (EVs) participate in PCa progression by conditioning the pre-metastatic niche. However, how EVs mediate the cross-talk between PCa cells and osteoprogenitors in the bone microenvironment remains poorly understood. We found that EVs derived from murine PCa cell line RM1-BM increased metabolic activity, vitality, and cell proliferation of osteoblast precursors by >60%, while significantly impairing mineral deposition (-37%). The latter was further confirmed in two complementary in vivo models of ossification. Accordingly, gene and protein set enrichments of osteoprogenitors exposed to EVs displayed significant downregulation of osteogenic markers and upregulation of proinflammatory factors. Additionally, transcriptomic profiling of PCa-EVs revealed the abundance of three microRNAs, miR-26a-5p, miR-27a-3p, and miR-30e-5p involved in the suppression of BMP-2-induced osteogenesis in vivo, suggesting the critical role of these EV-derived miRNAs in PCa-mediated suppression of osteoblast activity. Taken together, our results indicate the importance of EV cargo in cancer-bone cross-talk in vitro and in vivo and suggest that exosomal miRNAs may contribute to the onset of osteosclerotic bone lesions in PCa.

Indexed as

AnimalsBone and BonesCell CommunicationCell Line, TumorCell ProliferationExosome Multienzyme Ribonuclease ComplexExosomesExtracellular VesiclesGene ExpressionGene Expression ProfilingGene Expression Regulation, NeoplasticMaleMesenchymal Stem CellsMiceMice, Inbred C57BLMicroRNAsExosome Multienzyme Ribonuclease ComplexMicroRNAsbone metastasesextracellular vesiclesmiRNAosteoprogenitorsprostate cancer

Identifiers

PMID35163219
PMCPMC8836054
OpenAlexW4210307141

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.