Evidence map›Paper›PMID 38832305›Full record

ArticleBioactive materials2024

β-catenin mRNA encapsulated in SM-102 lipid nanoparticles enhances bone formation in a murine tibia fracture repair model.

Anna Laura Nelson, Chiara Mancino, Xueqin Gao, Joshua A Choe, Laura Chubb, Katherine Williams, Molly Czachor, Ralph Marcucio, Francesca Taraballi, John P Cooke and 3 more

Abstract read
In one paragraph

Article in Bioactive materials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

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  9. What's New in Musculoskeletal Basic Science.The Journal of bone and joint surgery. American volume · 2025
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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

13 authors.

Anna Laura NelsonSteadman Philippon Research Institute (SPRI), Center for Regenerative and Personalized Medicine, Vail, CO, USA.
Chiara MancinoHouston Methodist Research Institute, Center for Musculoskeletal Regeneration, Houston TX, USA.
Xueqin GaoSteadman Philippon Research Institute (SPRI), Center for Regenerative and Personalized Medicine, Vail, CO, USA.
Joshua A ChoeUniversity of Wisconsin-Madison, Department of Orthopedics and Rehabilitation, Department of Biomedical Engineering, Medical Scientist Training Program, Madison, WI, USA.
Laura ChubbColorado State University, Department of Clinical Sciences, Fort Collins CO, USA.
Katherine WilliamsColorado State University, Department of Microbiology, Immunology, and Pathology, Fort Collins, CO, USA.
Molly CzachorSteadman Philippon Research Institute (SPRI), Center for Regenerative and Personalized Medicine, Vail, CO, USA.
Ralph MarcucioUniversity of California, San Francisco (UCSF), Orthopaedic Trauma Institute, San Francisco, CA, USA.
Francesca TaraballiHouston Methodist Research Institute, Center for Musculoskeletal Regeneration, Houston TX, USA.
John P CookeHouston Methodist Research Institute, Center for RNA Therapeutics, Department of Cardiovascular Sciences, Houston, TX, USA.
Johnny HuardSteadman Philippon Research Institute (SPRI), Center for Regenerative and Personalized Medicine, Vail, CO, USA.
Chelsea BahneySteadman Philippon Research Institute (SPRI), Center for Regenerative and Personalized Medicine, Vail, CO, USA.
Nicole EhrhartColorado State University, School of Biomedical Engineering, Fort Collins CO, USA.

Funding

Integrated Training For Physician-ScientistsT32GM140935 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Anna Huttenlocher, Jeniel E Nett · 2021 to 2026
$6.5M
Therapeutic Application of Painless Nerve Growth Factor to Accelerate Endochondral Fracture RepairR01AR077761 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BAHNEY, CHELSEA SHIELDS · 2021 to 2025
$3.2M
Mineral Coated Microparticles for Stabilization and Delivery of Complexed mRNA for Healing of Long Bone DefectsF30AG077748 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI CHOE, JOSHUA ALAN · 2022 to 2024
$87k
NIAMS NIH HHS R01 AR077761NIA NIH HHS F30 AG077748NIGMS NIH HHS T32 GM140935
6 · The paper itself

Abstract

Fractures continue to be a global economic burden as there are currently no osteoanabolic drugs approved to accelerate fracture healing. In this study, we aimed to develop an osteoanabolic therapy which activates the Wnt/β-catenin pathway, a molecular driver of endochondral ossification. We hypothesize that using an mRNA-based therapeutic encoding β-catenin could promote cartilage to bone transformation formation by activating the canonical Wnt signaling pathway in chondrocytes. To optimize a delivery platform built on recent advancements in liposomal technologies, two FDA-approved ionizable phospholipids, DLin-MC3-DMA (MC3) and SM-102, were used to fabricate unique ionizable lipid nanoparticle (LNP) formulations and then tested for transfection efficacy both

Indexed as

Canonical WntFracture healingGene therapyLipid nanoparticlesmRNA

Identifiers

PMID38832305
PMCPMC11145078

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.