Evidence map›Paper›PMID 34070449›Full record

ArticleInternational journal of molecular sciences2021

Repression of MUC1 Promotes Expansion and Suppressive Function of Myeloid-Derived Suppressor Cells in Pancreatic and Breast Cancer Murine Models.

Mahnaz Sahraei, Mukulika Bose, J Alexa Sanders, Chandrav De, Lopamudra DasRoy, Sritama Nath, Cory R Brouwer, Pinku Mukherjee

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. 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
1.2field-weighted citation impact, top 22% 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, 17 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

8 authors at 2 institutions in 1 country.

Mahnaz SahraeiDepartment of Bioinformatics, Yale University, New Haven, CT 06520, USA.
Mukulika BoseDepartment of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC 28223, USA.ORCID 0000-0002-2347-7413
J Alexa SandersDepartment of Bioinformatics, University of North Carolina at Charlotte, Charlotte, NC 28223, USA.
Chandrav DeDepartment of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC 28223, USA.
Lopamudra DasRoyDepartment of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC 28223, USA.
Sritama NathWunderman Thompson Health IMsci, Cary, NC 27519, USA.
Cory R BrouwerDepartment of Bioinformatics, University of North Carolina at Charlotte, Charlotte, NC 28223, USA.
Pinku MukherjeeDepartment of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC 28223, USA.
University of North Carolina at Charlotte · USYale University · US

Funding

NCI NIH HHS CA166910; CA118944University of North Carolina at Charlotte Belk Endowment at UNCC
6 · The paper itself

Abstract

Myeloid-derived suppressor cells (MDSCs) are immature myeloid cells that are responsible for immunosuppression in tumor microenvironment. Here we report the impact of mucin 1 (MUC1), a transmembrane glycoprotein, on proliferation and functional activity of MDSCs. To determine the role of MUC1 in MDSC phenotype, we analyzed MDSCs derived from wild type (WT) and MUC1-knockout (MUC1KO) mice bearing syngeneic pancreatic (KCKO) or breast (C57MG) tumors. We observed enhanced tumor growth of pancreatic and breast tumors in the MUC1KO mice compared to the WT mice. Enhanced tumor growth in the MUC1KO mice was associated with increased numbers of suppressive MDSCs and T regulatory (Tregs) cells in the tumor microenvironment. Compared to the WT host, MUC1KO host showed higher levels of iNOS, ARG1, and TGF-β, thus promoting proliferation of MDSCs with an immature and immune suppressive phenotype. When co-cultured with effector T cells, MDSCs from MUC1KO mice led to higher repression of IL-2 and IFN-γ production by T cells as compared to MDSCs from WT mice. Lastly, MDSCs from MUC1KO mice showed higher levels of c-Myc and activated pSTAT3 as compared to MDSCs from WT mice, suggesting increased survival, proliferation, and prevention of maturation of MDSCs in the MUC1KO host. We report diminished T cell function in the KO versus WT mice. In summary, the data suggest that MUC1 may regulate signaling pathways that are critical to maintain the immunosuppressive properties of MDSCs.

Indexed as

AnimalsBreast NeoplasmsCell Line, TumorCell MovementCell ProliferationCoculture TechniquesDisease Models, AnimalFemaleInterferon-gammaInterleukin-2MaleMiceMice, Inbred C57BLMice, KnockoutMucin-1Myeloid-Derived Suppressor CellsInterferon-gammaInterleukin-2muc1 protein, mouseMucin-1Myc protein, mouseProto-Oncogene Proteins c-mycStat3 protein, mouseSTAT3 Transcription FactorTransforming Growth Factor betabreast cancerc–MYCimmune suppressioniNOSMDSCsMUC1pancreatic cancerpSTAT3TGFβTregs

Identifiers

PMID34070449
PMCPMC8197523
OpenAlexW3165579366

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.