Evidence map›Paper›PMID 32587616›Full record

ArticleJournal of oncology2020

Bovine Dialyzable Leukocyte Extract IMMUNEPOTENT-CRP Induces Selective ROS-Dependent Apoptosis in T-Acute Lymphoblastic Leukemia Cell Lines.

Helen Yarimet Lorenzo-Anota, Ana Carolina Martínez-Torres, Daniel Scott-Algara, Reyes S Tamez-Guerra, Cristina Rodríguez-Padilla

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Journal of oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06676709 (Effect of IMMUNEPOTENT-CRP, a Bovine Dialyzable Leukocyte Extract, on Serum Pro-Inflammatory Cytokines in Outpatients with Mild to Moderate COVID-19), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 35% 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.

NCT06676709 phase1 / phase2completednot on this mapstarted 2021, after this paper: background citation

Effect of IMMUNEPOTENT-CRP, a Bovine Dialyzable Leukocyte Extract, on Serum Pro-Inflammatory Cytokines in Outpatients with Mild to Moderate COVID-19: a Randomized, Double-Blind, Placebo-Controlled Study

TypeinterventionalSponsorUniversidad Autonoma de Nuevo LeonRan2021 to 2022Enrolled80ConditionsCOVID-19, SARS-CoV2 InfectionArmsIMMUNEPOTENT-CRP (I-CRP), Placebo Comparator
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. 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.

Helen Yarimet Lorenzo-AnotaUniversidad Autónoma de Nuevo León, Facultad de Ciencias Biologicas, Laboratorio de Inmunología y Virología, San Nicolás De Los Garza, Mexico.ORCID https://orcid.org/0000-0001-9560-4357
Ana Carolina Martínez-TorresUniversidad Autónoma de Nuevo León, Facultad de Ciencias Biologicas, Laboratorio de Inmunología y Virología, San Nicolás De Los Garza, Mexico.ORCID https://orcid.org/0000-0002-6183-0089
Daniel Scott-AlgaraUnité de Biologie Cellulaire des Lymphocytes, Institut Pasteur, Paris, France.
Reyes S Tamez-GuerraUniversidad Autónoma de Nuevo León, Facultad de Ciencias Biologicas, Laboratorio de Inmunología y Virología, San Nicolás De Los Garza, Mexico.ORCID https://orcid.org/0000-0001-5759-0863
Cristina Rodríguez-PadillaUniversidad Autónoma de Nuevo León, Facultad de Ciencias Biologicas, Laboratorio de Inmunología y Virología, San Nicolás De Los Garza, Mexico.
Universidad Autónoma de Nuevo León · MXInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapies strengthen the immune system to fight multiple diseases such as infections, immunodeficiencies, and autoimmune diseases, and recently, they are being used as an adjuvant in cancer treatment. IMMUNEPOTENT-CRP (I-CRP) is an immunotherapy made of bovine dialyzable leukocyte extract (bDLE) that has chemoprotective and immunomodulatory effects in different cellular populations of the immune system and antitumor activity in different cancer cell lines. Our recent results suggest that the antineoplastic effect of I-CRP is due to the characteristics of cancer cells. To confirm, we evaluated whether the selectivity is due to cell lineage or characteristics of cancer cells, testing cytotoxicity in T-acute lymphoblastic leukemia cells and their cell death mechanism. Here, we assessed the effect of I-CRP on cell viability and cell death. To determine the mechanism of cell death, we tested cell cycle, mitochondrial and nuclear alterations, and caspases and reactive oxygen species (ROS) and their role in cell death mechanism. Our results show that I-CRP does not affect cell viability in noncancer cells and induces selective cytotoxicity in a dose-dependent manner in leukemic cell lines. I-CRP also induces mitochondrial damage through proapoptotic and antiapoptotic protein modulation (Bax and Bcl-2) and ROS production, nuclear alterations including DNA damage (

Identifiers

PMID32587616
PMCPMC7298273
OpenAlexW3034026414

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.