Evidence map›Paper›PMID 34727170›Full record

ArticleBlood advances2022

Decreased IL-10 accelerates B-cell leukemia/lymphoma in a mouse model of pediatric lymphoid leukemia.

Briana A Fitch, Mi Zhou, Jamilla Situ, Sangeetha Surianarayanan, Melissa Q Reeves, Michelle L Hermiston, Joseph L Wiemels, Scott C Kogan

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

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  10. Nlp-dependent ER-to-Golgi transport.International journal of biological sciences · 2024
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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

8 authors at 3 institutions in 1 country.

Briana A FitchDepartment of Laboratory Medicine.
Mi ZhouDepartment of Laboratory Medicine.
Jamilla SituDepartment of Laboratory Medicine.
Sangeetha SurianarayananDepartment of Laboratory Medicine.
Melissa Q ReevesHelen Diller Family Comprehensive Cancer Center, and.ORCID 0000-0002-4886-5164
Michelle L HermistonHelen Diller Family Comprehensive Cancer Center, and.
Joseph L WiemelsCenter for Genetic Epidemiology, Department of Preventive Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, CA.
Scott C KoganDepartment of Laboratory Medicine.ORCID 0000-0002-2395-8479
University of California, San Francisco · USUCSF Helen Diller Family Comprehensive Cancer Center · USUniversity of Southern California · US

Funding

Impact of low IL-10 levels at birth and leukemia riskR01CA185058 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KOGAN, SCOTT C., WIEMELS, JOSEPH LEO · 2014 to 2018
$3.1M
Mechanism of IL-10 protective effect in development of childhood B cell acute lymphoblastic leukemiaF31CA221157 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FITCH, BRIANA · 2017 to 2019
$104k
NCI NIH HHS F31 CA221157NCI NIH HHS R01 CA185058
6 · The paper itself

Abstract

Exposures to a wide repertoire of common childhood infections and strong inflammatory responses to those infections are associated with the risk of pediatric B-cell acute lymphoblastic leukemia (B-ALL) in opposing directions. Neonatal inflammatory markers are also related to risk by unknown mechanism(s). Here, we demonstrate that interleukin-10 (IL-10) deficiency, which is associated with childhood B-ALL, indirectly impairs B lymphopoiesis and increases B-cell DNA damage in association with a module of 6 proinflammatory/myeloid-associated cytokines (IL-1α, IL-6, IL-12p40, IL-13, macrophage inflammatory protein-1β/CCL4, and granulocyte colony-stimulating factor). Importantly, antibiotics attenuated inflammation and B-cell defects in preleukemic Cdkn2a-/-Il10-/- mice. In an ETV6-RUNX1+ (E6R1+) Cdkn2a-/- mouse model of B-ALL, decreased levels of IL-10 accelerated B-cell neoplasms in a dose-dependent manner and altered the mutational profile of these neoplasms. Our results illuminate a mechanism through which a low level of IL-10 can create a risk for leukemic transformation and support developing evidence that microbial dysbiosis contributes to pediatric B-ALL.

Indexed as

Leukemia, B-CellLeukemia, Lymphocytic, Chronic, B-CellLymphomaPrecursor Cell Lymphoblastic Leukemia-LymphomaAnimalsChildDisease Models, AnimalHumansInterleukin-10MiceIL10 protein, mouseInterleukin-10

Identifiers

PMID34727170
PMCPMC8945291
OpenAlexW3208882125

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.