Evidence map›Paper›PMID 34207500›Full record

ReviewInternational journal of molecular sciences2021

4-1BBL as a Mediator of Cross-Talk between Innate, Adaptive, and Regulatory Immunity against Cancer.

Alejandra G Martinez-Perez, Jose J Perez-Trujillo, Rodolfo Garza-Morales, Maria J Loera-Arias, Odila Saucedo-Cardenas, Aracely Garcia-Garcia, Humberto Rodriguez-Rocha, Roberto Montes-de-Oca-Luna

Open access · goldAbstract readReview
In one paragraph

Review 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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.8field-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

13 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Personalizing Oncolytic Immunovirotherapy Approaches.Molecular diagnosis & therapy · 2024
    Article
  8. Terminally exhausted CD8Immunity & ageing : I & A · 2023
    Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
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 3 institutions in 2 countries.

Alejandra G Martinez-PerezDepartment of Histology, School of Medicine, Autonomous University of Nuevo Leon, Monterrey 64460, Mexico.ORCID 0000-0001-8535-3910
Jose J Perez-TrujilloDepartment of Histology, School of Medicine, Autonomous University of Nuevo Leon, Monterrey 64460, Mexico.
Rodolfo Garza-MoralesInternal Medicine Residency Program, University of Texas Rio Grande Valley, Edinburg, TX 78539, USA.ORCID 0000-0002-3613-521X
Maria J Loera-AriasDepartment of Histology, School of Medicine, Autonomous University of Nuevo Leon, Monterrey 64460, Mexico.ORCID 0000-0001-9561-3624
Odila Saucedo-CardenasDepartment of Histology, School of Medicine, Autonomous University of Nuevo Leon, Monterrey 64460, Mexico.
Aracely Garcia-GarciaDepartment of Histology, School of Medicine, Autonomous University of Nuevo Leon, Monterrey 64460, Mexico.ORCID 0000-0002-1699-9678
Humberto Rodriguez-RochaDepartment of Histology, School of Medicine, Autonomous University of Nuevo Leon, Monterrey 64460, Mexico.ORCID 0000-0003-0486-7448
Roberto Montes-de-Oca-LunaDepartment of Histology, School of Medicine, Autonomous University of Nuevo Leon, Monterrey 64460, Mexico.ORCID 0000-0001-8253-680X
Universidad Autónoma de Nuevo León · MXMexican Social Security Institute · MXThe University of Texas Rio Grande Valley · US

Funding

Consejo Nacional de Ciencia y Tecnología 754332
6 · The paper itself

Abstract

The ability of tumor cells to evade the immune system is one of the main challenges we confront in the fight against cancer. Multiple strategies have been developed to counteract this situation, including the use of immunostimulant molecules that play a key role in the anti-tumor immune response. Such a response needs to be tumor-specific to cause as little damage as possible to healthy cells and also to track and eliminate disseminated tumor cells. Therefore, the combination of immunostimulant molecules and tumor-associated antigens has been implemented as an anti-tumor therapy strategy to eliminate the main obstacles confronted in conventional therapies. The immunostimulant 4-1BBL belongs to the tumor necrosis factor (TNF) family and it has been widely reported as the most effective member for activating lymphocytes. Hence, we will review the molecular, pre-clinical, and clinical applications in conjunction with tumor-associated antigens in antitumor immunotherapy, as well as the main molecular pathways involved in this association.

Indexed as

Immunity, InnateLymphocyte Activation4-1BB LigandAnimalsAntigens, NeoplasmHumansNeoplasm ProteinsNeoplasms4-1BB LigandAntigens, NeoplasmNeoplasm ProteinsTNFSF9 protein, human4-1BBLcancer immunologycancer therapycancer vaccinationimmunotherapy

Identifiers

PMID34207500
PMCPMC8227424
OpenAlexW3166674305

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.