Evidence map›Paper›PMID 31275386›Full record

ArticleJournal of oncology2019

PKHB1 Tumor Cell Lysate Induces Antitumor Immune System Stimulation and Tumor Regression in Syngeneic Mice with Tumoral T Lymphoblasts.

Ana Carolina Martínez-Torres, Kenny Misael Calvillo-Rodríguez, Ashanti Concepción Uscanga-Palomeque, Luis Gómez-Morales, Rodolfo Mendoza-Reveles, Diana Caballero-Hernández, Philippe Karoyan, Cristina Rodríguez-Padilla

Open access · hybridAbstract read
In one paragraph

Article in Journal of oncology, 2019. 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
0.9field-weighted citation impact, top 27% 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, 15 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Role of CD47 in Hematological Malignancies.Journal of hematology & oncology · 2020
    Review
  10. Article
  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

8 authors at 2 institutions in 2 countries.

Ana Carolina Martínez-TorresUniversidad Autónoma de Nuevo León, Facultad de Ciencias Biologicas, Laboratorio de Inmunología y Virología, Mexico.ORCID 0000-0002-6183-0089
Kenny Misael Calvillo-RodríguezUniversidad Autónoma de Nuevo León, Facultad de Ciencias Biologicas, Laboratorio de Inmunología y Virología, Mexico.ORCID 0000-0001-7289-6166
Ashanti Concepción Uscanga-PalomequeUniversidad Autónoma de Nuevo León, Facultad de Ciencias Biologicas, Laboratorio de Inmunología y Virología, Mexico.ORCID 0000-0003-3258-5157
Luis Gómez-MoralesUniversidad Autónoma de Nuevo León, Facultad de Ciencias Biologicas, Laboratorio de Inmunología y Virología, Mexico.ORCID 0000-0002-2014-9617
Rodolfo Mendoza-RevelesUniversidad Autónoma de Nuevo León, Facultad de Ciencias Biologicas, Laboratorio de Inmunología y Virología, Mexico.
Diana Caballero-HernándezUniversidad Autónoma de Nuevo León, Facultad de Ciencias Biologicas, Laboratorio de Inmunología y Virología, Mexico.
Philippe KaroyanSorbonne Université, École Normale Supérieure, PSL University, CNRS, Laboratoire des Biomolécules, 75005 Paris, France.ORCID 0000-0003-1525-6474
Cristina Rodríguez-PadillaUniversidad Autónoma de Nuevo León, Facultad de Ciencias Biologicas, Laboratorio de Inmunología y Virología, Mexico.
Universidad Autónoma de Nuevo León · MXCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute lymphocytic leukemia (ALL) is the most common pediatric cancer. Currently, treatment options for patients with relapsed and refractory ALL mostly rely on immunotherapies. However, hematological cancers are commonly associated with a low immunogenicity and immune tolerance, which may contribute to leukemia relapse and the difficulties associated with the development of effective immunotherapies against this disease. We recently demonstrated that PKHB1, a TSP1-derived CD47 agonist peptide, induces immunogenic cell death (ICD) in T cell ALL (T-ALL). Cell death induced by PKHB1 on T-ALL cell lines and their homologous murine, L5178Y-R (T-murine tumor lymphoblast cell line), induced damage-associated molecular patterns (DAMPs) exposure and release. Additionally, a prophylactic vaccination with PKHB1-treated L5178Y-R cells prevented tumor establishment

Identifiers

PMID31275386
PMCPMC6582786
OpenAlexW2948548570

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.