Evidence map›Paper›PMID 35767377›Full record

ArticleAdvanced healthcare materials2022

A 3D Osteosarcoma Model with Bone-Mimicking Cues Reveals a Critical Role of Bone Mineral and Informs Drug Discovery.

Eva C González Díaz, Alex G Lee, Leanne C Sayles, Criselle Feria, E Alejandro Sweet-Cordero, Fan Yang

Open access · greenAbstract read
In one paragraph

Article in Advanced healthcare materials, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.8field-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

22 citing papers in PubMed, 28 citations in OpenAlex.

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  20. Engineered bone marrow as a clinically relevant ex vivo model for primary bone cancer research and drug screening.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

6 authors at 2 institutions in 1 country.

Eva C González DíazDepartment of Bioengineering, Stanford University, Stanford, CA, 94305, USA.ORCID 0000-0002-6170-148X
Alex G LeeDivision of Oncology, Department of Pediatrics, University of California San Francisco, San Francisco, California, 94143, USA.
Leanne C SaylesDivision of Oncology, Department of Pediatrics, University of California San Francisco, San Francisco, California, 94143, USA.
Criselle FeriaDepartment of Bioengineering, Stanford University, Stanford, CA, 94305, USA.
E Alejandro Sweet-CorderoDivision of Oncology, Department of Pediatrics, University of California San Francisco, San Francisco, California, 94143, USA.
Fan YangDepartment of Bioengineering, Stanford University, Stanford, CA, 94305, USA.ORCID 0000-0002-0418-0403
Stanford University · USUniversity of California, San Francisco · US

Funding

Microribbon scaffold-mediated Immunomodulation for Cranial Bone RepairR01DE024772 · NIDCR · STANFORD UNIVERSITY · PI YANG, FAN · 2015 to 2025
$4.6M
Development of Advanced Preclinical Models for Pediatric Solid TumorsR01CA243555 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SWEET-CORDERO, ERIC ALEJANDRO, VASKE, OLENA MOROZOVA · 2020 to 2024
$3.0M
Sliding hydrogels for accelerating cartilage regenerationR01AR074502 · NIAMS · STANFORD UNIVERSITY · PI YANG, FAN · 2019 to 2023
$2.2M
NCI NIH HHS R01 CA243555NCI NIH HHS R01CA243555NIAMS NIH HHS R01 AR074502NIDCR NIH HHS R01 DE024772
6 · The paper itself

Abstract

Osteosarcoma (OS) is an aggressive bone cancer for which survival has not improved over three decades. While biomaterials have been widely used to engineer 3D soft-tissue tumor models, the potential of engineering 3D biomaterials-based OS models for comprehensive interrogation of OS pathology and drug discovery remains untapped. Bone is characterized by high mineral content, yet the role of bone mineral in OS progression and drug response remains unknown. Here, a microribbon-based OS model with bone-mimicking compositions is developed to elucidate the role of 3D culture and hydroxyapatite in OS signaling and drug response. The results reveal that hydroxyapatite in 3D is critical to support retention of OS signaling and drug resistance similar to patient tissues and mouse orthotopic tumors. The physiological relevance of this 3D model is validated using four established OS cell lines, seven patient-derived xenograft (PDX) cell lines and two animal models. Integrating 3D OS PDX models with RNA-sequencing identified 3D-specific druggable target, which predicts drug response in mouse orthotopic model. These results establish microribbon-based 3D OS models as a novel experimental tool to enable discovery of novel therapeutics that would be otherwise missed with 2D model and may serve as platforms to study patient-specific OS heterogeneity and drug resistance mechanisms.

Indexed as

Bone NeoplasmsOsteosarcomaAnimalsBiocompatible MaterialsCell Line, TumorCuesDrug DiscoveryHumansHydroxyapatitesMiceMineralsBiocompatible MaterialsHydroxyapatitesMineralsbone mineralsdrug discoveryhigh-dimensional sequencingmicroribbonosteosarcomapatient-derived xenograft cellsthree-dimensional cancer models

Identifiers

PMID35767377
PMCPMC10162498
OpenAlexW4283730894

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.