Evidence map›Paper›PMID 32587277›Full record

ArticleScientific reports2020

NTAL is associated with treatment outcome, cell proliferation and differentiation in acute promyelocytic leukemia.

Carolina Hassibe Thomé, Germano Aguiar Ferreira, Diego Antonio Pereira-Martins, Guilherme Augusto Dos Santos, César Alexander Ortiz, Lucas Eduardo Botelho de Souza, Lays Martins Sobral, Cleide Lúcia Araújo Silva, Priscila Santos Scheucher, Cristiane Damas Gil and 26 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 37% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Review
  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

36 authors at 18 institutions in 8 countries.

Carolina Hassibe Thomé *Department of Biochemistry and Immunology, Medical School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.
Germano Aguiar Ferreira *Department of Biochemistry and Immunology, Medical School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.
Diego Antonio Pereira-Martins *Regional Blood Center of Ribeirão Preto, Medical School of Ribeirão Preto, Center for Cell Based Therapy, University of São Paulo, Ribeirão Preto, Brazil.ORCID http://orcid.org/0000-0002-3302-4311
Guilherme Augusto Dos SantosRegional Blood Center of Ribeirão Preto, Medical School of Ribeirão Preto, Center for Cell Based Therapy, University of São Paulo, Ribeirão Preto, Brazil.
César Alexander OrtizRegional Blood Center of Ribeirão Preto, Medical School of Ribeirão Preto, Center for Cell Based Therapy, University of São Paulo, Ribeirão Preto, Brazil.
Lucas Eduardo Botelho de SouzaRegional Blood Center of Ribeirão Preto, Medical School of Ribeirão Preto, Center for Cell Based Therapy, University of São Paulo, Ribeirão Preto, Brazil.ORCID http://orcid.org/0000-0003-4254-7509
Lays Martins SobralDepartment of Clinical Analyses, Toxicology and Food Sciences, University of São Paulo, Ribeirão Preto, Brazil.
Cleide Lúcia Araújo SilvaRegional Blood Center of Ribeirão Preto, Medical School of Ribeirão Preto, Center for Cell Based Therapy, University of São Paulo, Ribeirão Preto, Brazil.
Priscila Santos ScheucherRegional Blood Center of Ribeirão Preto, Medical School of Ribeirão Preto, Center for Cell Based Therapy, University of São Paulo, Ribeirão Preto, Brazil.
Cristiane Damas GilDepartment of Morphology and Genetics, Federal University of São Paulo, São Paulo, Brazil.
Andréia Machado LeopoldinoDepartment of Clinical Analyses, Toxicology and Food Sciences, University of São Paulo, Ribeirão Preto, Brazil.ORCID http://orcid.org/0000-0002-8313-4754
Douglas R A SilveiraHematology, Medical School, University of São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-5298-9592
Juan L Coelho-SilvaRegional Blood Center of Ribeirão Preto, Medical School of Ribeirão Preto, Center for Cell Based Therapy, University of São Paulo, Ribeirão Preto, Brazil.
Fabíola TrainaRegional Blood Center of Ribeirão Preto, Medical School of Ribeirão Preto, Center for Cell Based Therapy, University of São Paulo, Ribeirão Preto, Brazil.ORCID http://orcid.org/0000-0003-4258-289X
Luisa C KouryRegional Blood Center of Ribeirão Preto, Medical School of Ribeirão Preto, Center for Cell Based Therapy, University of São Paulo, Ribeirão Preto, Brazil.
Raul A M MeloDepartment of Internal Medicine, University of Pernambuco, Recife, Brazil.
Rosane BittencourtHematology Division, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.
Katia PagnanoHematology and Hemotherapy Center, University of Campinas, Campinas, Brazil.
Ricardo PasquiniHematology Division, Federal University of Paraná, Curitiba, Brazil.
Elenaide C NunesHematology Division, Federal University of Paraná, Curitiba, Brazil.ORCID http://orcid.org/0000-0002-1444-2542
Evandro M FagundesHematology Division, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Ana Beatriz F GloriaHematology Division, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Fábio Rodrigues KerbauyFederal University of São Paulo, São Paulo, Brazil.
Maria de Lourdes ChauffailleFederal University of São Paulo, São Paulo, Brazil.
Armand KeatingCell Therapy Program, Princess Margaret Cancer Centre, Toronto, Canada.
Martin S TallmanLeukemia Service, Memorial Sloan-Kettering Cancer Center/Weill Cornell Medical College, New York, USA.
Raul C RibeiroDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, USA.ORCID http://orcid.org/0000-0002-9956-5647
Richard DillonDepartment of Medical and Molecular Genetics, King's College London School of Medicine, London, UK.
Arnold GanserDepartment of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
Bob LöwenbergDepartment of Hematology, Erasmus University Medical Center, Rotterdam, Netherlands.
Peter ValkSanta Lucia Foundation, Rome, Italy.
Francesco Lo-CocoDepartment of Biopathology, Tor Vergata University, Rome, Italy.
Miguel A SanzDepartment of Hematology, Valencia University Medical School, Valencia, Spain.
Nancy BerlinerDepartment of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, USA.ORCID http://orcid.org/0000-0001-7502-6895
Vitor Marcel Faça *Department of Biochemistry and Immunology, Medical School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.ORCID http://orcid.org/0000-0003-3205-7944
Eduardo M Rego *Regional Blood Center of Ribeirão Preto, Medical School of Ribeirão Preto, Center for Cell Based Therapy, University of São Paulo, Ribeirão Preto, Brazil. eduardo.rego@fm.usp.br.ORCID http://orcid.org/0000-0003-1567-4086
Universidade de São Paulo · BRUniversidade Federal de São Paulo · BRUniversidade Federal de Minas Gerais · BRUniversidade Federal do Paraná · BRBrigham and Women's Hospital · USErasmus MC · NLFondazione Santa Lucia · ITKing's College London · GBMedizinische Hochschule Hannover · DEMemorial Sloan Kettering Cancer Center · USPrincess Margaret Cancer Centre · CASt. Jude Children's Research Hospital · USUniversidade de Pernambuco · BRUniversidade de Ribeirão Preto · BRUniversidade Estadual de Campinas (UNICAMP) · BRUniversidade Federal do Rio Grande do Sul · BRUniversitat de València · ESUniversity of Rome Tor Vergata · IT

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Non-T cell activation linker (NTAL) is a lipid raft-membrane protein expressed by normal and leukemic cells and involved in cell signaling. In acute promyelocytic leukemia (APL), NTAL depletion from lipid rafts decreases cell viability through regulation of the Akt/PI3K pathway. The role of NTAL in APL cell processes, and its association with clinical outcome, has not, however, been established. Here, we show that reduced levels of NTAL were associated with increased all-trans retinoic acid (ATRA)-induced differentiation, generation of reactive oxygen species, and mitochondrial dysfunction. Additionally, NTAL-knockdown (NTAL-KD) in APL cell lines led to activation of Ras, inhibition of Akt/mTOR pathways, and increased expression of autophagy markers, leading to an increased apoptosis rate following arsenic trioxide treatment. Furthermore, NTAL-KD in NB4 cells decreased the tumor burden in (NOD scid gamma) NSG mice, suggesting its implication in tumor growth. A retrospective analysis of NTAL expression in a cohort of patients treated with ATRA and anthracyclines, revealed that NTAL overexpression was associated with a high leukocyte count (P = 0.007) and was independently associated with shorter overall survival (Hazard Ratio: 3.6; 95% Confidence Interval: 1.17-11.28; P = 0.026). Taken together, our data highlights the importance of NTAL in APL cell survival and response to treatment.

Indexed as

Adaptor Proteins, Signal TransducingAdolescentAdultAgedAnimalsAnthracyclinesAntineoplastic Combined Chemotherapy ProtocolsBone MarrowCell DifferentiationCell Line, TumorCell ProliferationCell SurvivalDisease-Free SurvivalFemaleGene Knockdown TechniquesHumansAdaptor Proteins, Signal TransducingAnthracyclinesLAT2 protein, humanTretinoin

Identifiers

PMID32587277
PMCPMC7316767
OpenAlexW3037638198

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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.