Evidence map›Paper›PMID 38125724›Full record

ArticleOncoimmunology2024

Clusterin protects mature dendritic cells from reactive oxygen species mediated cell death.

Alvaro López Malizia, Antonela Merlotti, Pierre-Emmanuel Bonte, Melina Sager, Yago Arribas De Sandoval, Christel Goudot, Fernando Erra Díaz, Pehuén Pereyra-Gerber, Ana Ceballos, Sebastian Amigorena and 2 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2024. 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
2.5field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Tumor Microenvironment in Melanoma-Characteristic and Clinical Implications.International journal of molecular sciences · 2025
    Review
  8. Article
  9. Article
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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

12 authors at 3 institutions in 3 countries.

Alvaro López MaliziaInstituto de Investigaciones Biomédicas en Retrovirus y SIDA (INBIRS), Buenos Aires University, School of Medicine, Buenos Aires, Argentina.
Antonela MerlottiInstitut Curie, Université Paris Sciences et Lettres, Paris, France.
Pierre-Emmanuel BonteInstitut Curie, Université Paris Sciences et Lettres, Paris, France.
Melina SagerInstituto de Investigaciones Biomédicas en Retrovirus y SIDA (INBIRS), Buenos Aires University, School of Medicine, Buenos Aires, Argentina.
Yago Arribas De SandovalInstitut Curie, Université Paris Sciences et Lettres, Paris, France.
Christel GoudotInstitut Curie, Université Paris Sciences et Lettres, Paris, France.
Fernando Erra DíazInstituto de Investigaciones Biomédicas en Retrovirus y SIDA (INBIRS), Buenos Aires University, School of Medicine, Buenos Aires, Argentina.
Pehuén Pereyra-GerberCambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Department of Medicine, University of Cambridge, Cambridge, UK.
Ana CeballosInstituto de Investigaciones Biomédicas en Retrovirus y SIDA (INBIRS), Buenos Aires University, School of Medicine, Buenos Aires, Argentina.
Sebastian AmigorenaInstitut Curie, Université Paris Sciences et Lettres, Paris, France.
Jorge GeffnerInstituto de Investigaciones Biomédicas en Retrovirus y SIDA (INBIRS), Buenos Aires University, School of Medicine, Buenos Aires, Argentina.
Juan SabatteInstituto de Investigaciones Biomédicas en Retrovirus y SIDA (INBIRS), Buenos Aires University, School of Medicine, Buenos Aires, Argentina.
Instituto de Investigaciones Biomédicas en Retrovirus y Sida · ARInstitut Curie · FRUniversity of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs) play a key role in the induction of the adaptive immune response. They capture antigens in peripheral tissues and prime naïve T lymphocytes, triggering the adaptive immune response. In the course of inflammatory processes DCs face stressful conditions including hypoxia, low pH and high concentrations of reactive oxygen species (ROS), among others. How DCs survive under these adverse conditions remain poorly understood. Clusterin is a protein highly expressed by tumors and usually associated with bad prognosis. It promotes cancer cell survival by different mechanisms such as apoptosis inhibition and promotion of autophagy. Here, we show that, upon maturation, human monocyte-derived DCs (MoDCs) up-regulate clusterin expression. Clusterin protects MoDCs from ROS-mediated toxicity, enhancing DC survival and promoting their ability to induce T cell activation. In line with these results, we found that clusterin is expressed by a population of mature LAMP3+ DCs, called mregDCs, but not by immature DCs in human cancer. The expression of clusterin by intratumoral DCs was shown to be associated with a transcriptomic profile indicative of cellular response to stress. These results uncover an important role for clusterin in DC physiology.

Indexed as

ClusterinNeoplasmsCell DeathDendritic CellsHumansReactive Oxygen SpeciesT-LymphocytesCLU protein, humanClusterinReactive Oxygen SpeciesCancerclusterindendritic cellsmregDCRos

Identifiers

PMID38125724
PMCPMC10730137
OpenAlexW4389918080

What OpenQuestion holds

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LicenceCC BY-NC
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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.