Evidence map›Paper›PMID 34737747›Full record

ArticleFrontiers in immunology2021

Patient-Derived Bone Marrow Spheroids Reveal Leukemia-Initiating Cells Supported by Mesenchymal Hypoxic Niches in Pediatric B-ALL.

Juan Carlos Balandrán, José Dávila-Velderrain, Antonio Sandoval-Cabrera, Gabriela Zamora-Herrera, Vanessa Terán-Cerqueda, Lilia Adela García-Stivalet, José Alejandro Limón-Flores, Erick Armenta-Castro, Aurora Rodríguez-Martínez, Bertha Alicia Leon-Chavez and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 24 citations in OpenAlex.

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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

16 authors at 9 institutions in 2 countries.

Juan Carlos BalandránLaboratorio de Oncoinmunología y Citómica, Centro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social Delegación Puebla, Puebla, Mexico.
José Dávila-VelderrainComputer Science and Artificial Intelligence Lab, Massachusetts Institute of Technology (MIT), Cambridge, MA, United States.
Antonio Sandoval-CabreraHospital para el Niño de Toluca, Instituto Materno Infantil del Estado de México (IMIEM), Toluca, Mexico.
Gabriela Zamora-HerreraLaboratorio de Oncoinmunología y Citómica, Centro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social Delegación Puebla, Puebla, Mexico.
Vanessa Terán-CerquedaServicio de Hematología, Unidad Médica de Alta Especialidad, Hospital de Especialidades "Manuel Ávila Camacho", Instituto Mexicano del Seguro Social, Puebla, Mexico.
Lilia Adela García-StivaletServicio de Hematología, Unidad Médica de Alta Especialidad, Hospital de Especialidades "Manuel Ávila Camacho", Instituto Mexicano del Seguro Social, Puebla, Mexico.
José Alejandro Limón-FloresServicio de Hematología, Unidad Médica de Alta Especialidad, Hospital de Especialidades "Manuel Ávila Camacho", Instituto Mexicano del Seguro Social, Puebla, Mexico.
Erick Armenta-CastroLaboratorio de Oncoinmunología y Citómica, Centro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social Delegación Puebla, Puebla, Mexico.
Aurora Rodríguez-MartínezLaboratorio de Oncoinmunología y Citómica, Centro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social Delegación Puebla, Puebla, Mexico.
Bertha Alicia Leon-ChavezPosgrado en Ciencias Químicas, Area de Bioquímica y Biología Molecular, Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.
Verónica Vallejo-RuizLaboratorio de Oncoinmunología y Citómica, Centro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social Delegación Puebla, Puebla, Mexico.
Duane C HassaneDivision of Hematology and Medical Oncology, Department of Medicine, Weill Cornell Medicine, New York, NY, United States.
Sonia Mayra Pérez-TapiaUnidad de Desarrollo e Investigación en Bioprocesos (UDIBI) and Unidad de Investigación, Desarrollo e Innovación Médica y Biotecnológica (UDIMEB), Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Mexico City, Mexico.
Vianney Ortiz-NavarreteDepartamento de Biomedicina Molecular, Centro de Investigación y de Estudios Avanzados (CINVESTAV), Mexico City, Mexico.
Monica L GuzmanDivision of Hematology and Medical Oncology, Department of Medicine, Weill Cornell Medicine, New York, NY, United States.
Rosana PelayoLaboratorio de Oncoinmunología y Citómica, Centro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social Delegación Puebla, Puebla, Mexico.
Mexican Social Security Institute · MXCenter for Research and Advanced Studies of the National Polytechnic Institute · MXBenemérita Universidad Autónoma de Puebla · MXCornell University · USHospital de Especialidades · MXInstituto de Salud del Estado de México · MXInstituto Politécnico Nacional · MXMassachusetts Institute of Technology · USWeill Cornell Medicine · US

Funding

Targeted Small Molecule Inhibitors for Inv(16) LeukemiaR01CA234478 · NCI · UNIVERSITY OF VIRGINIA · PI BUSHWELLER, JOHN HACKETT, CASTILLA, LUCIO H. · 2019 to 2023
$3.4M
3D co-culture system to characterize and target leukemia stem cellsR21CA245454 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI GUZMAN, MONICA L · 2020 to 2020
$436k
NCI NIH HHS R01 CA234478NCI NIH HHS R21 CA245454
6 · The paper itself

Abstract

B-cell acute lymphoblastic leukemia (B-ALL) results from the expansion of malignant lymphoid precursors within the bone marrow (BM), where hematopoietic niches and microenvironmental signals provide leukemia-initiating cells (LICs) the conditions to survive, proliferate, initiate disease, and relapse. Normal and malignant lymphopoiesis are highly dependent on the BM microenvironment, particularly on CXCL12-abundant Reticular (CAR) cells, which provide a niche for maintenance of primitive cells. During B-ALL, leukemic cells hijack BM niches, creating a proinflammatory milieu incompetent to support normal hematopoiesis but favoring leukemic proliferation. Although the lack of a phenotypic stem cell hierarchy is apparent in B-ALL, LICs are a rare and quiescent population potentially responsible for chemoresistance and relapse. Here, we developed novel patient-derived leukemia spheroids (PDLS), an

Indexed as

Spheroids, CellularStem Cell NicheTumor Cells, CulturedAnimalsBone MarrowFemaleHeterograftsHumansMesenchymal Stem CellsMiceNeoplastic Stem CellsPrecursor Cell Lymphoblastic Leukemia-LymphomaTumor Microenvironmentacute lymphoblastic leukemiaB-cell developmentbone marrow nicheleukemia-initiating cellmesenchymal stromal cellstumor microenvironment

Identifiers

PMID34737747
PMCPMC8561951
OpenAlexW3207664429

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.