Evidence map›Paper›PMID 38381833›Full record

ArticleScience advances2024

From breast cancer cell homing to the onset of early bone metastasis: The role of bone (re)modeling in early lesion formation.

Sarah A E Young, Anna-Dorothea Heller, Daniela S Garske, Maximilian Rummler, Victoria Qian, Agnes Ellinghaus, Georg N Duda, Bettina M Willie, Anika Grüneboom, Amaia Cipitria

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2024. 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
4.0field-weighted citation impact, top 5% 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, 15 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

10 authors at 5 institutions in 3 countries.

Sarah A E YoungDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, Potsdam, Germany.ORCID 0000-0003-3862-3863
Anna-Dorothea HellerDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, Potsdam, Germany.ORCID 0009-0000-7497-9045
Daniela S GarskeDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, Potsdam, Germany.ORCID 0000-0002-9784-0756
Maximilian RummlerDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, Potsdam, Germany.ORCID 0000-0002-0788-7172
Victoria QianDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, Potsdam, Germany.ORCID 0000-0001-9711-5290
Agnes EllinghausJulius Wolff Institute, Berlin Institute of Health at Charité-Universitätsmedizin Berlin, Germany.ORCID 0000-0002-8849-2227
Georg N DudaJulius Wolff Institute, Berlin Institute of Health at Charité-Universitätsmedizin Berlin, Germany.ORCID 0000-0001-7605-3908
Bettina M WillieResearch Centre, Shriners Hospital for Children-Canada, Faculty of Dental Medicine and Oral Health Sciences, McGill University, Montreal, Canada.ORCID 0000-0003-2907-3580
Anika GrüneboomLeibniz-Institute for Advancing Analytics - ISAS - e.V., Dortmund, Germany.ORCID 0000-0002-7928-5613
Amaia CipitriaDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, Potsdam, Germany.ORCID 0000-0002-9918-1512
Max Planck Institute of Colloids and Interfaces · DEBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DEMcGill University Health Centre · CAIkerbasque · ESLeibniz Institute for Analytical Sciences - ISAS · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer often metastasizes to bone, causing osteolytic lesions. Structural and biophysical changes are rarely studied yet are hypothesized to influence metastasis. We developed a mouse model of early bone metastasis and multimodal imaging to quantify cancer cell homing, bone (re)modeling, and onset of metastasis. Using tissue clearing and three-dimensional (3D) light sheet fluorescence microscopy, we located enhanced green fluorescent protein-positive cancer cells and small clusters in intact bones and quantified their size and spatial distribution. We detected early bone lesions using in vivo microcomputed tomography (microCT)-based time-lapse morphometry and revealed altered bone (re)modeling in the absence of detectable lesions. With a new microCT image analysis tool, we tracked the growth of early lesions over time. We showed that cancer cells home in all bone compartments, while osteolytic lesions are only detected in the metaphysis, a region of high (re)modeling. Our study suggests that higher rates of (re)modeling act as a driver of lesion formation during early metastasis.

Indexed as

Bone NeoplasmsOsteolysisAnimalsBone and BonesCell Line, TumorDisease Models, AnimalMiceX-Ray Microtomography

Identifiers

PMID38381833
PMCPMC10881061
OpenAlexW4391992221

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.