Evidence map›Paper›PMID 39513364›Full record

ArticleJCI insight2024

Thrombopoietin mimetic reduces mouse lung inflammation and fibrosis after radiation by attenuating activated endothelial phenotypes.

Jeb English, Sriya Dhanikonda, Kathryn E Tanaka, Wade Koba, Gary Eichenbaum, Weng-Lang Yang, Chandan Guha

Abstract read
In one paragraph

Article in JCI insight, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Article
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  5. Radiomitigators: Breakthroughs in Post-Radiation Recovery.Antioxidants (Basel, Switzerland) · 2026
    Review
  6. Article
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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

7 authors.

Jeb EnglishDepartment of Radiation Oncology.
Sriya DhanikondaDepartment of Radiation Oncology.
Kathryn E TanakaDepartment of Pathology, and.
Wade KobaDepartment of Radiology, Albert Einstein College of Medicine, Bronx, New York, USA.
Gary EichenbaumOffice of the Chief Medical Officer, Johnson & Johnson, New Brunswick, New Jersey, USA.
Weng-Lang YangDepartment of Radiation Oncology.
Chandan GuhaDepartment of Radiation Oncology.

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI THOMAS E ROHAN · 1985 to 2026
$111.2M
Stromal cell therapy as a treatment against Gastrointestinal Acute Radiation Syndrome (GI-ARS)U01AI138324 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI GUHA, CHANDAN · 2018 to 2022
$2.9M
Development of thrombopoietin mimetic (TPOm) as a mitigator against Radiation-induced endovascular injuriesU01AI133608 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI GHOSH, SANCHITA P, GUHA, CHANDAN · 2017 to 2021
$2.4M
Bigfoot Multispectral High Speed Fluorescence Activated Cell SorterS10OD032169 · OD · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI PORCELLI, STEVEN A · 2022 to 2022
$600k
Cytek Aurora Multiparameter Flow CytometerS10OD026833 · OD · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI PORCELLI, STEVEN A · 2019 to 2019
$367k
High-speed/resolution whole slide scanner supported by two core facilitiesS10OD019961 · OD · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI CONDEELIS, JOHN S · 2015 to 2015
$326k
NCI NIH HHS P30 CA013330NIAID NIH HHS U01 AI133608NIAID NIH HHS U01 AI138324NIH HHS S10 OD019961NIH HHS S10 OD026833NIH HHS S10 OD032169
6 · The paper itself

Abstract

Radiation-induced lung injury (RILI) initiates radiation pneumonitis and progresses to fibrosis as the main side effect experienced by patients with lung cancer treated with radiotherapy. There is no effective drug for RILI. Sustained vascular activation is a major contributor to the establishment of chronic disease. Here, using a whole thoracic irradiation (WTI) mouse model, we investigated the mechanisms and effectiveness of thrombopoietin mimetic (TPOm) for preventing RILI. We demonstrated that administering TPOm 24 hours before irradiation decreased histologic lung injury score, apoptosis, vascular permeability, expression of proinflammatory cytokines, and neutrophil infiltration in the lungs of mice 2 weeks after WTI. We described the expression of c-MPL, a TPO receptor, in mouse primary pulmonary microvascular endothelial cells, showing that TPOm reduced endothelial cell-neutrophil adhesion by inhibiting ICAM-1 expression. Seven months after WTI, TPOm-treated lung exhibited less collagen deposition and expression of MMP-9, TIMP-1, IL-6, TGF-β, and p21. Moreover, TPOm improved lung vascular structure, lung density, and respiration rate, leading to a prolonged survival time after WTI. Single-cell RNA sequencing analysis of lungs 2 weeks after WTI revealed that TPOm shifted populations of capillary endothelial cells toward a less activated and more homeostatic phenotype. Taken together, TPOm is protective for RILI by inhibiting endothelial cell activation.

Indexed as

Endothelial CellsRadiation PneumonitisThrombopoietinAnimalsDisease Models, AnimalFemaleHumansIntercellular Adhesion Molecule-1LungMiceMice, Inbred C57BLNeutrophilsPhenotypePulmonary FibrosisIntercellular Adhesion Molecule-1ThrombopoietinEndothelial cellsFibrosisPulmonologyRadiation therapyTherapeutics

Identifiers

PMID39513364
PMCPMC11601560

What OpenQuestion holds

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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.