Evidence map›Paper›PMID 30723587›Full record

ArticleOncoimmunology

Nuclear receptor ligands induce TREM-1 expression on dendritic cells: analysis of their role in tumors.

Raffaella Fontana, Laura Raccosta, Lucrezia Rovati, Knut R Steffensen, Aida Paniccia, Tomas Jakobsson, Giulio Melloni, Alessandro Bandiera, Giorgia Mangili, Alice Bergamini and 8 more

Abstract read
In one paragraph

Article in Oncoimmunology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. The biology of TREM receptors.Nature reviews. Immunology · 2023
    Review
  5. Article
  6. Clinical relevance of tumour-associated macrophages.Nature reviews. Clinical oncology · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. 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

18 authors.

Raffaella FontanaImmuno-Biotherapy of Melanoma and Solid Tumors Unit, Division of Experimental Oncology, IRCCS Scientific Institute San Raffaele, Milan, Italy.
Laura RaccostaImmuno-Biotherapy of Melanoma and Solid Tumors Unit, Division of Experimental Oncology, IRCCS Scientific Institute San Raffaele, Milan, Italy.ORCID 0000-0002-1625-9573
Lucrezia RovatiImmuno-Biotherapy of Melanoma and Solid Tumors Unit, Division of Experimental Oncology, IRCCS Scientific Institute San Raffaele, Milan, Italy.
Knut R SteffensenDepartment of Biosciences and Nutrition, Karolinska Institute, Huddinge, Sweden.
Aida PanicciaImmuno-Biotherapy of Melanoma and Solid Tumors Unit, Division of Experimental Oncology, IRCCS Scientific Institute San Raffaele, Milan, Italy.
Tomas JakobssonDepartment of Biosciences and Nutrition, Karolinska Institute, Huddinge, Sweden.
Giulio MelloniThoracic Surgery Unit, IRCCS Scientific Institute San Raffaele, Milan, Italy.
Alessandro BandieraThoracic Surgery Unit, IRCCS Scientific Institute San Raffaele, Milan, Italy.
Giorgia MangiliGynecologic Unit, IRCCS Scientific Institute San Raffaele, Milan, Italy.
Alice BergaminiGynecologic Unit, IRCCS Scientific Institute San Raffaele, Milan, Italy.
Daniela MaggioniImmuno-Biotherapy of Melanoma and Solid Tumors Unit, Division of Experimental Oncology, IRCCS Scientific Institute San Raffaele, Milan, Italy.
Claudio DoglioniDepartment of Pathology, IRCCS Scientific Institute San Raffaele, Milan, Italy.
Roberto CrocchioloHematology Unit, ASST Bergamo Ovest, Treviglio, Italy.
Marina CellaDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, MO, USA.
Michela MattioliDepartment of Medical Biotechnology and Translational Medicine (BIOMETRA), University of Milan, Segrate, Italy.
Cristina BattagliaDepartment of Medical Biotechnology and Translational Medicine (BIOMETRA), University of Milan, Segrate, Italy.ORCID 0000-0003-3025-9657
Marco ColonnaDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, MO, USA.
Vincenzo RussoImmuno-Biotherapy of Melanoma and Solid Tumors Unit, Division of Experimental Oncology, IRCCS Scientific Institute San Raffaele, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs) initiate adaptive immune responses after their migration to secondary lymphoid organs. The LXR ligands/oxysterols and the RXR ligand 9-cis Retinoic Acid (9-cis RA) were shown to dampen DC migration to lymphoid organs through the inhibition of CCR7 expression. We performed transcriptomics of DCs undergoing maturation in the presence of the LXR ligand 22R-Hydroxycholesterol (22R-HC). The analysis highlighted more than 1500 genes modulated by 22R-HC treatment, including the triggering receptor expressed on myeloid cells (TREM)-1, which was found markedly up-regulated. We tested the effect of other nuclear receptor ligands (NRL) and we reported the induction of TREM-1 following RXR, RAR and VDR activation. From a functional point of view, triggering of TREM-1 induced by retinoids increased TNFα and IL-1β release, suggesting an active role of NRL-activated TREM-1

Indexed as

dendritic cellslung cancerLXR nuclear receptorsovarian cancerRAR/RXR nuclear receptorsTREM-1

Identifiers

PMID30723587
PMCPMC6350683

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.