Evidence map›Paper›PMID 37446353›Full record

ArticleInternational journal of molecular sciences2023

Tumor-Suppressive and Immunomodulating Activity of miR-30a-3p and miR-30e-3p in HNSCC Cells and Tumoroids.

Ombline Conrad, Mickaël Burgy, Sophie Foppolo, Aude Jehl, Alicia Thiéry, Sébastien Guihard, Romain Vauchelles, Alain C Jung, Jana Mourtada, Christine Macabre and 9 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Trial
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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 4 institutions in 1 country.

Ombline ConradLaboratory of Bioimaging and Pathology, University of Strasbourg, UMR7021 CNRS, 67401 Illkirch, France.ORCID 0000-0001-7438-5394
Mickaël BurgyLaboratory of Bioimaging and Pathology, University of Strasbourg, UMR7021 CNRS, 67401 Illkirch, France.ORCID 0000-0001-5724-3677
Sophie FoppoloLaboratory of Bioimaging and Pathology, University of Strasbourg, UMR7021 CNRS, 67401 Illkirch, France.ORCID 0000-0002-3167-8362
Aude JehlLaboratory of Bioimaging and Pathology, University of Strasbourg, UMR7021 CNRS, 67401 Illkirch, France.ORCID 0000-0003-0440-2704
Alicia ThiéryDepartment of Public Health, Institut de Cancérologie Strasbourg Europe, 67200 Strasbourg, France.
Sébastien GuihardDepartment of Radiotherapy, Institut de Cancérologie Strasbourg Europe, 67200 Strasbourg, France.
Romain VauchellesLaboratory of Bioimaging and Pathology, University of Strasbourg, UMR7021 CNRS, 67401 Illkirch, France.
Alain C JungLaboratory STREINTH, Inserm IRFAC U1113, Université de Strasbourg, 67200 Strasbourg, France.
Jana MourtadaLaboratory STREINTH, Inserm IRFAC U1113, Université de Strasbourg, 67200 Strasbourg, France.ORCID 0000-0002-1000-0771
Christine MacabreLaboratory STREINTH, Inserm IRFAC U1113, Université de Strasbourg, 67200 Strasbourg, France.
Sonia LedrappierLaboratory STREINTH, Inserm IRFAC U1113, Université de Strasbourg, 67200 Strasbourg, France.
Marie-Pierre ChenardDepartment of Pathology, Strasbourg University Hospital, 67200 Strasbourg, France.
Mihaela-Alina OneaDepartment of Pathology, Strasbourg University Hospital, 67200 Strasbourg, France.
Aurélien DanicDepartment of Otolaryngology and Cervico-Facial Surgery, Strasbourg University Hospital, 67200 Strasbourg, France.
Thomas DourlhesDepartment of Otolaryngology and Cervico-Facial Surgery, Strasbourg University Hospital, 67200 Strasbourg, France.
Claire ThibaultDepartment of Otolaryngology and Cervico-Facial Surgery, Strasbourg University Hospital, 67200 Strasbourg, France.
Philippe SchultzDepartment of Otolaryngology and Cervico-Facial Surgery, Strasbourg University Hospital, 67200 Strasbourg, France.
Monique DontenwillLaboratory of Bioimaging and Pathology, University of Strasbourg, UMR7021 CNRS, 67401 Illkirch, France.ORCID 0000-0002-5235-3014
Sophie MartinLaboratory of Bioimaging and Pathology, University of Strasbourg, UMR7021 CNRS, 67401 Illkirch, France.ORCID 0000-0002-2907-7445
Centre National de la Recherche Scientifique · FRUniversité de Strasbourg · FRInserm · FRInstitut de Cancérologie Strasbourg · FR

Funding

Ligue Nationale Contre le Cancer No S19R417B
6 · The paper itself

Abstract

Head and neck squamous cell carcinomas (HNSCCs) are heterogeneous tumors, well known for their frequent relapsing nature. To counter recurrence, biomarkers for early diagnosis, prognosis, or treatment response prediction are urgently needed. miRNAs can profoundly impact normal physiology and enhance oncogenesis. Among all of the miRNAs, the miR-30 family is frequently downregulated in HNSCC. Here, we determined how levels of the 3p passenger strands of miR-30a and miR-30e affect tumor behavior and clarified their functional role in LA-HNSCC. In a retrospective study, levels of miR-30a-3p and miR-30e-3p were determined in 110 patients and correlated to overall survival, locoregional relapse, and distant metastasis. miR-30a/e-3p were expressed in HNSCC cell lines and HNSCC patient-derived tumoroids (PDTs) to investigate their effect on tumor cells and their microenvironment. Both miRNAs were found to have a prognosis value since low miR-30a/e-3p expression correlates to adverse prognosis and reduces overall survival. Low expression of miR-30a/e-3p is associated with a shorter time until locoregional relapse and a shorter time until metastasis, respectively. miR-30a/e-3p expression downregulates both TGF-βR1 and BMPR2 and attenuates the survival and motility of HNSCC. Results were confirmed in PDTs. Finally, secretomes of miR-30a/e-3p-transfected HNSCC activate M1-type macrophages, which exert stronger phagocytic activities toward tumor cells. miR-30a/e-3p expression can discriminate subgroups of LA-HNSCC patients with different prognosis, making them good candidates as prognostic biomarkers. Furthermore, by targeting members of the TGF-β family and generating an immune-permissive microenvironment, they may emerge as an alternative to anti-TGF-β drugs to use in combination with immune checkpoint inhibitors.

Indexed as

Head and Neck NeoplasmsMicroRNAsGene Expression Regulation, NeoplasticHumansNeoplasm Recurrence, LocalRetrospective StudiesSquamous Cell Carcinoma of Head and NeckTumor MicroenvironmentMicroRNAsbiomarkershead and neck cancersmicroRNAphagocytosistumoroid

Identifiers

PMID37446353
PMCPMC10342301
OpenAlexW4383536377

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.