Evidence map›Paper›PMID 38829115›Full record

ArticleAnnals of surgery2025

Elucidating the Mechanism of Radiation Therapy on Mesenchymal Cell Fate in Preventing Heterotopic Ossification.

Meng-Lun Hsieh, Ji Hae Choi, Sneha Korlakunta, Yuanyuan Zhang, Benjamin Levi

Abstract read
In one paragraph

Article in Annals of surgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Review
  4. 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

5 authors.

Meng-Lun HsiehDepartment of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX.
Ji Hae ChoiDepartment of Surgery, Center for Organogenesis Research and Trauma, University of Texas Southwestern Medical Center, Dallas, TX.
Sneha KorlakuntaDepartment of Surgery, Center for Organogenesis Research and Trauma, University of Texas Southwestern Medical Center, Dallas, TX.
Yuanyuan ZhangDepartment of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX.
Benjamin LeviDepartment of Surgery, Center for Organogenesis Research and Trauma, University of Texas Southwestern Medical Center, Dallas, TX.

Funding

UT Southwestern Center for Translational MedicineKL2TR003981 · NCATS · UT SOUTHWESTERN MEDICAL CENTER · PI ARGENBRIGHT, KEITH EDWARD, TRIVEDI, MADHUKAR H. · 2021 to 2025
$5.9M
Targeting jmjd3 mitigates heterotopic ossificationR01AR079863 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Katherine Ann Gallagher, Benjamin Levi · 2021 to 2026
$3.0M
NCATS NIH HHS KL2 TR003981NIAMS NIH HHS R01 AR079863
6 · The paper itself

Abstract

objectiveTo recapitulate the use of radiation in preventing heterotopic ossification (HO) in an animal model to thereby mechanistically investigate radiation-induced changes at the single-cell level.

backgroundHO is the formation of extra-skeletal bone in abnormal areas including muscle and soft tissue. Radiation therapy is a clinically proven, localized preventive measure for HO. Despite its efficacy, there is a lack of standardization of radiation prescription; however, the mechanism of the impact of radiation on HO prevention remains unknown.

methodsC57BL6J male mice underwent burn/tenotomy with and without perioperative radiation treatment. Single-cell RNA sequencing was performed to analyze downstream signaling after HO-forming injury. Immunofluorescence microscopy was used to visualize protein expression changes in HO progenitor cells. In vivo range of motion analyses, histological staining, and micro-computerized tomography were performed to investigate mature HO's effect on joint function and to characterize total HO structure and volume.

resultsIn one fraction, 7 Gy delivered to the injury site within 72 hours postoperatively significantly decreases HO formation and improves hindlimb range of motion. In-depth single-cell transcriptomic analyses with immunofluorescent staining demonstrate decreased cellular numbers, as well as aberrant endochondral differentiation and downregulation of associated upstream BMP and ALK4 signaling pathways in irradiated mesenchymal progenitor cells.

conclusionsOur study is the first to explore the mechanism of radiotherapy prophylaxis in the prevention of traumatic HO. Not only does radiation decreases total HO progenitor cell numbers but also reduces aberrant osteochondral differentiation at the injury site, thereby decreasing overall HO and improving joint function.

Indexed as

Mesenchymal Stem CellsOssification, HeterotopicAnimalsBurnsDisease Models, AnimalMaleMiceMice, Inbred C57BLTenotomyheterotopic ossification (HO)mesenchymal progenitor cellsradiation

Identifiers

PMID38829115
PMCPMC11726538

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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.