Evidence map›Paper›PMID 34291358›Full record

ArticleJournal of cancer research and clinical oncology2021

Knockdown of the prognostic cancer stem cell marker Musashi-1 decreases radio-resistance while enhancing apoptosis in hormone receptor-positive breast cancer cells via p21

Fabian M Troschel, Heike Palenta, Katrin Borrmann, Kristin Heshe, San Hue Hua, George W Yip, Ludwig Kiesel, Hans Theodor Eich, Martin Götte, Burkhard Greve

Open access · hybridAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 26 citations in OpenAlex.

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  11. CDKN1A/p21 in Breast Cancer: Part of the Problem, or Part of the Solution?International journal of molecular sciences · 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

10 authors at 2 institutions in 2 countries.

Fabian M TroschelDepartment of Radiation Oncology, University Hospital Münster, 48149, Münster, Germany. fabian.troschel@uni-muenster.de.ORCID http://orcid.org/0000-0001-5066-6650
Heike PalentaDepartment of Gynecology and Obstetrics, University Hospital Münster, 48149, Münster, Germany.
Katrin BorrmannDepartment of Radiation Oncology, University Hospital Münster, 48149, Münster, Germany.
Kristin HesheDepartment of Radiation Oncology, University Hospital Münster, 48149, Münster, Germany.
San Hue HuaDepartment of Anatomy, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, 117594, Singapore.
George W YipDepartment of Anatomy, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, 117594, Singapore.ORCID http://orcid.org/0000-0003-0152-0510
Ludwig KieselDepartment of Gynecology and Obstetrics, University Hospital Münster, 48149, Münster, Germany.
Hans Theodor EichDepartment of Radiation Oncology, University Hospital Münster, 48149, Münster, Germany.
Martin Götte *Department of Gynecology and Obstetrics, University Hospital Münster, 48149, Münster, Germany.ORCID http://orcid.org/0000-0003-2360-2496
Burkhard Greve *Department of Radiation Oncology, University Hospital Münster, 48149, Münster, Germany.ORCID http://orcid.org/0000-0002-0331-8108
University Hospital Münster · DENational University of Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWhile the stem cell marker Musashi-1 (MSI-1) has been identified as a key player in a wide array of malignancies, few findings exist on its prognostic relevance and relevance for cancer cell death and therapy resistance in breast cancer.

methodsFirst, we determined prognostic relevance of MSI-1 in database analyses regarding multiple survival outcomes. To substantiate findings, MSI-1 was artificially downregulated in MCF-7 breast cancer cells and implications for cancer stem cell markers, cell apoptosis and apoptosis regulator p21, proliferation and radiation response were analyzed via flow cytometry and colony formation. Radiation-induced p21 expression changes were investigated using a dataset containing patient samples obtained before and after irradiation and own in vitro experiments.

resultsMSI-1 is a negative prognostic marker for disease-free and distant metastasis-free survival in breast cancer and tends to negatively influence overall survival. MSI-1 knockdown downregulated stem cell gene expression and proliferation, but increased p21 levels and apoptosis. Similar to the MSI-1 knockdown effect, p21 expression was strongly increased after irradiation and was expressed at even higher levels in MSI-1 knockdown cells after irradiation. Finally, combined use of MSI-1 silencing and irradiation reduced cancer cell survival.

conclusionMSI-1 is a prognostic marker in breast cancer. MSI-1 silencing downregulates proliferation while increasing apoptosis. The anti-proliferation mediator p21 was upregulated independently after both MSI-1 knockdown and irradiation and even more after both treatments combined, suggesting synergistic potential. Radio-sensitization effects after combining radiation and MSI-1 knockdown underline the potential of MSI-1 as a therapeutic target.

Indexed as

AgedApoptosisBreast NeoplasmsCell ProliferationCyclin-Dependent Kinase Inhibitor p21Down-RegulationFemaleGene Knockdown TechniquesHumansMCF-7 CellsNeoplastic Stem CellsNerve Tissue ProteinsPrognosisRadiation ToleranceRNA-Binding ProteinsCDKN1A protein, humanCyclin-Dependent Kinase Inhibitor p21MSI1 protein, humanNerve Tissue ProteinsRNA-Binding ProteinsApoptosisBreast cancerMusashi-1p21Radio-resistanceRNA-binding proteins

Identifiers

PMID34291358
PMCPMC8484224
OpenAlexW3185637828

What OpenQuestion holds

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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.