Evidence map›Paper›PMID 36482448›Full record

ArticleCell communication and signaling : CCS2022

Neuromedin U secreted by colorectal cancer cells promotes a tumour-supporting microenvironment.

Patrycja Przygodzka, Kamila Soboska, Ewelina Sochacka, Marcin Pacholczyk, Marcin Braun, Hassan Kassassir, Izabela Papiewska-Pająk, Michal Kielbik, Joanna Boncela

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Cell communication and signaling : CCS, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

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  12. Ferroptosis, Metabolic Rewiring, and Endometrial Cancer.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

9 authors at 4 institutions in 1 country.

Patrycja Przygodzka *Institute of Medical Biology, Polish Academy of Sciences, Lodowa 106, 93-232, Lodz, Poland. pprzygodzka@cbm.pan.pl.ORCID 0000-0001-7529-8815
Kamila Soboska *Institute of Medical Biology, Polish Academy of Sciences, Lodowa 106, 93-232, Lodz, Poland.ORCID 0000-0002-4154-4464
Ewelina SochackaInstitute of Medical Biology, Polish Academy of Sciences, Lodowa 106, 93-232, Lodz, Poland.ORCID 0000-0002-4897-3341
Marcin PacholczykDepartment of Systems Biology and Engineering, Silesian University of Technology, Akademicka 16, 44-100, Gliwice, Poland.ORCID 0000-0002-9741-2137
Marcin BraunDepartment of Pathology, Medical University of Lodz, Pomorska 251, 92-213, Lodz, Poland.ORCID 0000-0003-3804-7042
Hassan KassassirInstitute of Medical Biology, Polish Academy of Sciences, Lodowa 106, 93-232, Lodz, Poland.ORCID 0000-0002-2713-9497
Izabela Papiewska-PająkInstitute of Medical Biology, Polish Academy of Sciences, Lodowa 106, 93-232, Lodz, Poland.ORCID 0000-0001-6116-3418
Michal KielbikInstitute of Medical Biology, Polish Academy of Sciences, Lodowa 106, 93-232, Lodz, Poland.ORCID 0000-0002-6211-8288
Joanna BoncelaInstitute of Medical Biology, Polish Academy of Sciences, Lodowa 106, 93-232, Lodz, Poland.ORCID 0000-0001-8419-7012
Institute for Medical Biology · PLUniversity of Łódź · PLMedical University of Lodz · PLSilesian University of Technology · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeuromedin U (NMU) was identified as one of the hub genes closely related to colorectal cancer (CRC) progression and was recently shown to be a motility inducer in CRC cells. Its autocrine signalling through specific receptors increases cancer cell migration and invasiveness. Because of insufficient knowledge concerning NMU accessibility and action in the tumour microenvironment, its role in CRC remains poorly understood and its potential as a therapeutic target is still difficult to define.

methodsNMU expression in CRC tissue was detected by IHC. Data from The Cancer Genome Atlas were used to analyse gene expression in CRC. mRNA and protein expression was detected by real-time PCR, immunoblotting or immunofluorescence staining and analysed using confocal microscopy or flow cytometry. Proteome Profiler was used to detect changes in the profiles of cytokines released by cells constituting tumour microenvironment after NMU treatment. NMU receptor activity was monitored by detecting ERK1/2 activation. Transwell cell migration, wound healing assay and microtube formation assay were used to evaluate the effects of NMU on the migration of cancer cells, human macrophages and endothelial cells.

resultsOur current study showed increased NMU levels in human CRC when compared to normal adjacent tissue. We detected a correlation between high NMUR1 expression and shorter overall survival of patients with CRC. We identified NMUR1 expression on macrophages, endothelial cells, platelets, and NMUR1 presence in platelet microparticles. We confirmed ERK1/2 activation by treatment of macrophages and endothelial cells with NMU, which induced pro-metastatic phenotypes of analysed cells and changed their secretome. Finally, we showed that NMU-stimulated macrophages increased the migratory potential of CRC cells.

conclusionsWe propose that NMU is involved in the modulation and promotion of the pro-metastatic tumour microenvironment in CRC through the activation of cancer cells and other tumour niche cells, macrophages and endothelial cells. Video abstract.

Indexed as

Colorectal NeoplasmsTumor MicroenvironmentEndothelial CellsHumansColorectal cancerEndothelial cellsMacrophagesNeuromedin UNMU receptors

Identifiers

PMID36482448
PMCPMC9733105
OpenAlexW4311580231

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.