Evidence map›Paper›PMID 31856674›Full record

ReviewStem cells and development2020

Immunoregulatory Potential of Exosomes Derived from Cancer Stem Cells.

Shannon M Clayton, Joehleen A Archard, Joseph Wagner, D Gregory Farwell, Arnaud F Bewley, Angela Beliveau, Andrew Birkeland, Shyam Rao, Marianne Abouyared, Peter C Belafsky and 1 more

Open access · hybridAbstract readReview
In one paragraph

Review in Stem cells and development, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

10 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

11 authors at 1 institution in 1 country.

Shannon M ClaytonDepartment of Otolaryngology, University of California, Davis, Sacramento, California.
Joehleen A ArchardDepartment of Otolaryngology, University of California, Davis, Sacramento, California.
Joseph WagnerUniversity of California Drug Discovery Consortium, University of California, Davis, Sacramento, California.
D Gregory FarwellDepartment of Otolaryngology, University of California, Davis, Sacramento, California.
Arnaud F BewleyDepartment of Otolaryngology, University of California, Davis, Sacramento, California.
Angela BeliveauDepartment of Otolaryngology, University of California, Davis, Sacramento, California.
Andrew BirkelandDepartment of Otolaryngology, University of California, Davis, Sacramento, California.
Shyam RaoDepartment of Otolaryngology, University of California, Davis, Sacramento, California.
Marianne AbouyaredDepartment of Otolaryngology, University of California, Davis, Sacramento, California.
Peter C BelafskyDepartment of Otolaryngology, University of California, Davis, Sacramento, California.
Johnathon D AndersonDepartment of Otolaryngology, University of California, Davis, Sacramento, California.
University of California, Davis · US

Funding

UC Davis Clinical and Translational Science CenterUL1TR001860 · NCATS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KENYON, NICHOLAS J., LYLES, COURTNEY REES · 2016 to 2025
$47.3M
Institutional Career Development Core (KL2)KL2TR001859 · NCATS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HOLMES, JAMES F. · 2016 to 2025
$10.1M
Training Program In Basic & Translational Cardiovascular ScienceT32HL086350 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Martin Cadeiras, David A. Liem · 2008 to 2026
$7.1M
NCATS NIH HHS KL2 TR001859NCATS NIH HHS UL1 TR001860NHLBI NIH HHS T32 HL086350
6 · The paper itself

Abstract

Head and neck squamous cell carcinomas (HNSCCs) are malignancies that originate in the mucosal lining of the upper aerodigestive tract. Despite advances in therapeutic interventions, survival rates among HNSCC patients have remained static for years. Cancer stem cells (CSCs) are tumor-initiating cells that are highly resistant to treatment, and are hypothesized to contribute to a significant fraction of tumor recurrences. Consequently, further investigations of how CSCs mediate recurrence may provide insights into novel druggable targets. A key element of recurrence involves the tumor's ability to evade immunosurveillance. Recent published reports suggest that CSCs possess immunosuppressive properties, however, the underlying mechanism have yet to be fully elucidated. To date, most groups have focused on the role of CSC-derived secretory proteins, such as cytokines and growth factors. Here, we review the established immunoregulatory role of exosomes derived from mixed tumor cell populations, and propose further study of CSC-derived exosomes may be warranted. Such studies may yield novel insights into new druggable targets, or lay the foundation for future exosome-based diagnostics.

Indexed as

Carcinoma, Squamous CellCell DifferentiationCell Self RenewalExosomesHead and Neck NeoplasmsHumansNeoplasm Recurrence, LocalNeoplastic Stem CellsSignal TransductionTumor Microenvironmentcancer stem cellsexosomeshead and neck cancerm2 macrophagesregulatory T lymphocytessecretory proteins

Identifiers

PMID31856674
PMCPMC7081244
OpenAlexW2995748627

What OpenQuestion holds

Textmetadata
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.