Evidence map›Paper›PMID 33381445›Full record

ArticleFrontiers in oncology2020

Comparative Analysis of Systemic and Tumor Microenvironment Proteomes From Children With B-Cell Acute Lymphocytic Leukemia at Diagnosis and After Induction Treatment.

Geise Ellen Broto, Stephany Corrêa, Fausto Celso Trigo, Everton Cruz Dos Santos, Fernanda Tomiotto-Pelissier, Wander Rogério Pavanelli, Guilherme Ferreira Silveira, Eliana Abdelhay, Carolina Panis

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

9 authors at 4 institutions in 1 country.

Geise Ellen BrotoPrograma de Pós-graduação em Patologia Clínica e Laboratorial, Universidade Estadual de Londrina, Londrina, Brazil.
Stephany CorrêaLaboratório de Células-Tronco, Centro de Transplante de Medula Óssea (CEMO), Instituto Nacional de Câncer, Rio de Janeiro, Brazil.
Fausto Celso TrigoPediatrics Department, Hospital do Câncer de Londrina, Londrina, Brazil.
Everton Cruz Dos SantosLaboratório de Células-Tronco, Centro de Transplante de Medula Óssea (CEMO), Instituto Nacional de Câncer, Rio de Janeiro, Brazil.
Fernanda Tomiotto-PelissierPrograma de Pós-graduação em Patologia Experimental Universidade Estadual de Londrina, Londrina, Brazil.
Wander Rogério PavanelliPrograma de Pós-graduação em Patologia Experimental Universidade Estadual de Londrina, Londrina, Brazil.
Guilherme Ferreira SilveiraFundação Osvaldo Cruz, Instituto Carlos Chagas, Curitiba, Brazil.
Eliana AbdelhayLaboratório de Células-Tronco, Centro de Transplante de Medula Óssea (CEMO), Instituto Nacional de Câncer, Rio de Janeiro, Brazil.
Carolina PanisPrograma de Pós-graduação em Patologia Clínica e Laboratorial, Universidade Estadual de Londrina, Londrina, Brazil.
Universidade Estadual de Londrina · BRInstituto Nacional do Câncer · BRFundação Carlos Chagas · BRUniversidade Estadual do Oeste do Paraná · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Among the childhood diseases, B-cell acute lymphocytic leukemia (B-ALL) is the most frequent type of cancer. Despite recent advances concerning disease treatment, cytotoxic chemotherapy remains the first line of treatment in several countries, and the modifications induced by such drugs in the organism are still poorly understood. In this context, the present study provided a comparative high-throughput proteomic analysis of the cumulative changes induced by chemotherapeutic drugs used in the induction phase of B-ALL treatment in both peripheral blood (PB) and bone marrow compartment (BM) samples. To reach this goal, PB and BM plasma samples were comparatively analyzed by using label-free proteomics at two endpoints: at diagnosis (D0) and the end of the cumulative induction phase treatment (D28). Proteomic data was available

Indexed as

B-acute lymphocytic leukemiachemotherapyinterferon-gammainterferon regulatory factor 3proteomicstransthyretintumor biology

Identifiers

PMID33381445
PMCPMC7769010
OpenAlexW3112733137

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.