Evidence map›Paper›PMID 37443350›Full record

ArticleBritish journal of cancer2023

MiR-662 is associated with metastatic relapse in early-stage breast cancer and promotes metastasis by stimulating cancer cell stemness.

Margherita Puppo, Manoj Kumar Valluru, Martine Croset, Davide Ceresa, Michele Iuliani, Ashrin Khan, Julien Wicinski, Emmanuelle Charafe-Jauffret, Christophe Ginestier, Francesco Pantano and 2 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

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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

12 authors at 5 institutions in 3 countries.

Margherita PuppoDepartment of Oncology and Metabolism, Medical School, University of Sheffield, Sheffield, UK. margherita.puppo@inserm.fr.ORCID 0000-0003-1409-9577
Manoj Kumar ValluruDepartment of Oncology and Metabolism, Medical School, University of Sheffield, Sheffield, UK.
Martine CrosetINSERM, Research Unit UMR_S1033, LyOS, Faculty of Medicine Lyon-Est, Lyon, France.
Davide CeresaIRCCS AOU San Martino, Università degli studi di Genova, Genova, Italy.
Michele IulianiMedical Oncology, Fondazione Policlinico Universitario Campus Bio-Medico, Via Alvaro del Portillo 200, 00128, Roma, Italy.
Ashrin KhanDepartment of Oncology and Metabolism, Medical School, University of Sheffield, Sheffield, UK.
Julien WicinskiAix-Marseille Univ, Inserm, CNRS, Institut Paoli-Calmettes, CRCM, Epithelial Stem Cells and Cancer Lab, "Equipe labellisée Ligue Contre le Cancer", Marseille, France.
Emmanuelle Charafe-JauffretAix-Marseille Univ, Inserm, CNRS, Institut Paoli-Calmettes, CRCM, Epithelial Stem Cells and Cancer Lab, "Equipe labellisée Ligue Contre le Cancer", Marseille, France.
Christophe GinestierAix-Marseille Univ, Inserm, CNRS, Institut Paoli-Calmettes, CRCM, Epithelial Stem Cells and Cancer Lab, "Equipe labellisée Ligue Contre le Cancer", Marseille, France.
Francesco PantanoMedical Oncology, Fondazione Policlinico Universitario Campus Bio-Medico, Via Alvaro del Portillo 200, 00128, Roma, Italy.
Penelope Dawn OttewellDepartment of Oncology and Metabolism, Medical School, University of Sheffield, Sheffield, UK.
Philippe ClézardinDepartment of Oncology and Metabolism, Medical School, University of Sheffield, Sheffield, UK. philippe.clezardin@inserm.fr.ORCID 0000-0003-0149-4463
Centre National de la Recherche Scientifique · FRUniversité Claude Bernard Lyon 1 · FRUniversity of Sheffield · GBUniversità Campus Bio-Medico · ITOspedale Policlinico San Martino · IT

Funding

Medical Research Council MR/P000096/1
6 · The paper itself

Abstract

backgroundBreast cancer (BC) metastasis, which often occurs in bone, contributes substantially to mortality. MicroRNAs play a fundamental role in BC metastasis, although microRNA-regulated mechanisms driving metastasis progression remain poorly understood.

methodsMiRome analysis in serum from BC patients was performed by TaqMan™ low-density array. MiR-662 was overexpressed following MIMIC-transfection or lentivirus transduction. Animal models were used to investigate the role of miR-662 in BC (bone) metastasis. The effect of miR-662-overexpressing BC cell conditioned medium on osteoclastogenesis was investigated. ALDEFLUOR assays were performed to study BC stemness. RNA-sequencing transcriptomic analysis of miR-662-overexpressing BC cells was performed to evaluate gene expression changes.

resultsHigh levels of hsa-miR-662 (miR-662) in serum from BC patients, at baseline (time of surgery), were associated with future recurrence in bone. At an early-stage of the metastatic disease, miR-662 could mask the presence of BC metastases in bone by inhibiting the differentiation of bone-resorbing osteoclasts. Nonetheless, metastatic miR-662-overexpressing BC cells then progressed as overt osteolytic metastases thanks to increased stem cell-like traits.

conclusionsMiR-662 is involved in BC metastasis progression, suggesting it may be used as a prognostic marker to identify BC patients at high risk of metastasis.

Indexed as

Bone NeoplasmsBreast NeoplasmsMicroRNAsAnimalsCell DifferentiationCell Line, TumorCell ProliferationGene Expression ProfilingGene Expression Regulation, NeoplasticHumansNeoplasm MetastasisNeoplasm Recurrence, LocalMicroRNAsMIRN662 microRNA, human

Identifiers

PMID37443350
PMCPMC10449914
OpenAlexW4384155639

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.