Evidence map›Paper›PMID 32054102›Full record

ReviewCells2020

Human Plasmacytoid Dendritic Cells and Cutaneous Melanoma.

Matilde Monti, Francesca Consoli, Raffaella Vescovi, Mattia Bugatti, William Vermi

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

24 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  3. Article
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  6. Correlation analysis between peripheral blood dendritic cell subsets and PD-1 in patients with peritoneal adenocarcinoma.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2024
    Article
  7. Review
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  14. High expression of lncRNAOncology letters · 2022
    Article
  15. Article
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  17. Review
  18. Type I Interferon Production of Plasmacytoid Dendritic Cells under Control.International journal of molecular sciences · 2021
    Review
  19. Article
  20. Article
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

5 authors at 2 institutions in 2 countries.

Matilde MontiDepartment of Molecular and Translational Medicine, University of Brescia, Brescia 25123, Italy.
Francesca ConsoliDepartment of Medical and Surgical Specialties, Radiological Sciences and Public Health, Medical Oncology, University of Brescia at ASST-Spedali Civili, Brescia 25123, Italy.
Raffaella VescoviDepartment of Molecular and Translational Medicine, University of Brescia, Brescia 25123, Italy.
Mattia BugattiDepartment of Molecular and Translational Medicine, University of Brescia, Brescia 25123, Italy.
William VermiDepartment of Molecular and Translational Medicine, University of Brescia, Brescia 25123, Italy.
University of Brescia · ITWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prognosis of metastatic melanoma (MM) patients has remained poor for a long time. However, the recent introduction of effective target therapies (BRAF and MEK inhibitors for BRAFV600-mutated MM) and immunotherapies (anti-CTLA-4 and anti-PD-1) has significantly improved the survival of MM patients. Notably, all these responses are highly dependent on the fitness of the host immune system, including the innate compartment. Among immune cells involved in cancer immunity, properly activated plasmacytoid dendritic cells (pDCs) exert an important role, bridging the innate and adaptive immune responses and directly eliminating cancer cells. A distinctive feature of pDCs is the production of high amount of type I Interferon (I-IFN), through the Toll-like receptor (TLR) 7 and 9 signaling pathway activation. However, published data indicate that melanoma-associated escape mechanisms are in place to hijack pDC functions. We have recently reported that pDC recruitment is recurrent in the early phases of melanoma, but the entire pDC compartment collapses over melanoma progression. Here, we summarize recent advances on pDC biology and function within the context of melanoma immunity.

Indexed as

Cutaneous Malignant MelanomaDendritic CellsHumansImmunotherapyInterferon Type IMAP Kinase Kinase KinasesMelanomaNeoplasm MetastasisProto-Oncogene Proteins B-rafSignal TransductionSkin NeoplasmsToll-Like Receptor 7Toll-Like Receptor 9BRAF protein, humanInterferon Type IMAP Kinase Kinase KinasesProto-Oncogene Proteins B-rafTLR7 protein, humanToll-Like Receptor 7Toll-Like Receptor 9cutaneous melanomaplasmacytoid dendritic cellsTLR

Identifiers

PMID32054102
PMCPMC7072514
OpenAlexW3005591282

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.