Evidence map›Paper›PMID 35163198›Full record

ArticleInternational journal of molecular sciences2022

microRNA-21 Regulates Stemness in Pancreatic Ductal Adenocarcinoma Cells.

Maria Mortoglou, Francesc Miralles, Elif Damla Arisan, Alwyn Dart, Stipo Jurcevic, Sigrun Lange, Pinar Uysal-Onganer

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 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.9field-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

27 citing papers in PubMed, 33 citations in OpenAlex.

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  18. Current cancer drug targets · 2024
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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

7 authors at 3 institutions in 2 countries.

Maria MortoglouCancer Research Group, School of Life Sciences, University of Westminster, London W1W 6UW, UK.ORCID 0000-0003-4394-4549
Francesc MirallesMolecular and Clinical Sciences, Cell Biology Research Centre, St. George's University of London, Cranmer Terrace, SW17ORE London, UK.ORCID 0000-0003-3069-2725
Elif Damla ArisanInstitution of Biotechnology, Gebze Technical University, Gebze 41400, Turkey.ORCID 0000-0002-4844-6381
Alwyn DartInstitute of Medical and Biomedical Education, St. George's University of London, Cranmer Terrace, London SW17 ORE, UK.ORCID 0000-0003-3801-8583
Stipo JurcevicDepartment of Biomedical Sciences, School of Life Sciences, University of Westminster, London W1W 6UW, UK.
Sigrun LangeTissue Architecture and Regeneration Research Group, School of Life Sciences, University of Westminster, London W1W 6UW, UK.ORCID 0000-0002-7193-3102
Pinar Uysal-OnganerCancer Research Group, School of Life Sciences, University of Westminster, London W1W 6UW, UK.ORCID 0000-0003-3190-8831
University of Westminster · GBSt George's, University of London · GBGebze Technical University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is the most common and aggressive type of pancreatic cancer (PCa) with a low survival rate. microRNAs (miRs) are endogenous, non-coding RNAs that moderate numerous biological processes. miRs have been associated with the chemoresistance and metastasis of PDAC and the presence of a subpopulation of highly plastic "stem"-like cells within the tumor, known as cancer stem cells (CSCs). In this study, we investigated the role of miR-21, which is highly expressed in Panc-1 and MiaPaCa-2 PDAC cells in association with CSCs. Following miR-21 knockouts (KO) from both MiaPaCa-2 and Panc-1 cell lines, reversed expressions of epithelial-mesenchymal transition (EMT) and CSCs markers were observed. The expression patterns of key CSC markers, including CD44, CD133, CX-C chemokine receptor type 4 (CXCR4), and aldehyde dehydrogenase-1 (ALDH1), were changed depending on miR-21 status. miR-21 (KO) suppressed cellular invasion of Panc-1 and MiaPaCa-2 cells, as well as the cellular proliferation of MiaPaCa-2 cells. Our data suggest that miR-21 is involved in the stemness of PDAC cells, may play roles in mesenchymal transition, and that miR-21 poses as a novel, functional biomarker for PDAC aggressiveness.

Indexed as

AdenocarcinomaCarcinoma, Pancreatic DuctalCell Line, TumorCell MovementCell ProliferationEpithelial-Mesenchymal TransitionGene ExpressionGene Expression Regulation, NeoplasticHumansHyaluronan ReceptorsMicroRNAsNeoplastic Stem CellsPancreatic NeoplasmsReceptors, CXCR4TranscriptomeCD44 protein, humanCXCR4 protein, humanHyaluronan ReceptorsMicroRNAsMIRN21 microRNA, humanReceptors, CXCR4cancer stem cellsepithelial–mesenchymal transitionmetastasismicroRNAsnon-coding RNAspancreatic ductal adenocarcinoma

Identifiers

PMID35163198
PMCPMC8835847
OpenAlexW4210513049

What OpenQuestion holds

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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.