Evidence map›Paper›PMID 36943734›Full record

ArticleeLife2023

Osteosarcoma-enriched transcripts paradoxically generate osteosarcoma-suppressing extracellular proteins.

Kexin Li, Qingji Huo, Nathan H Dimmitt, Guofan Qu, Junjie Bao, Pankita H Pandya, M Reza Saadatzadeh, Khadijeh Bijangi-Vishehsaraei, Melissa A Kacena, Karen E Pollok and 3 more

Open access · goldFull text read
In one paragraph

Article in eLife, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 9 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

13 authors at 3 institutions in 2 countries.

Kexin LiDepartment of Pharmacology, School of Pharmacy, Harbin Medical University, Harbin, China.
Qingji HuoDepartment of Pharmacology, School of Pharmacy, Harbin Medical University, Harbin, China.ORCID 0000-0003-0438-6812
Nathan H DimmittDepartment of Biomedical Engineering, Indiana University Purdue University Indianapolis, Indianapolis, United States.
Guofan QuDepartment of Orthopedic Surgery, Harbin Medical University Cancer Hospital, Harbin, China.
Junjie BaoDepartment of Orthopedic Surgery, Harbin Medical University Cancer Hospital, Harbin, China.
Pankita H PandyaIndiana University Simon Comprehensive Cancer Center, Indiana University School of Medicine, Indianapolis, United States.
M Reza SaadatzadehIndiana University Simon Comprehensive Cancer Center, Indiana University School of Medicine, Indianapolis, United States.
Khadijeh Bijangi-VishehsaraeiDepartment of Pediatric Hematology and Oncology, Indiana University School of Medicine, Indianapolis, United States.ORCID 0009-0009-2522-8806
Melissa A KacenaIndiana University Simon Comprehensive Cancer Center, Indiana University School of Medicine, Indianapolis, United States.ORCID 0000-0001-7293-0088
Karen E PollokIndiana University Simon Comprehensive Cancer Center, Indiana University School of Medicine, Indianapolis, United States.
Chien-Chi LinDepartment of Biomedical Engineering, Indiana University Purdue University Indianapolis, Indianapolis, United States.ORCID 0000-0002-4175-8796
Bai-Yan LiDepartment of Pharmacology, School of Pharmacy, Harbin Medical University, Harbin, China.
Hiroki YokotaDepartment of Biomedical Engineering, Indiana University Purdue University Indianapolis, Indianapolis, United States.ORCID 0000-0002-7881-8959
Indiana University School of MedicineUniversity of Indianapolis · USHarbin Medical University · CN

Funding

Tumor Microenvironment and Metastasis ProgramP30CA082709 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI Jun Wan · 1999 to 2026
$59.3M
Project 2: Biomarkers of endothelial dysfunction in pediatric patients receiving high intensity chemotherapy/irradiationP50HD090215 · NICHD · INDIANA UNIVERSITY INDIANAPOLIS · PI RENBARGER, JAMIE L · 2019 to 2020
$1.4M
Biomechanics and Biomaterials Research Center at Indiana University Purdue University Indianapolis, USA 2201-01NCI NIH HHS P30 CA082709NICHD NIH HHS P50 HD090215
6 · The paper itself

Abstract

Osteosarcoma (OS) is the common primary bone cancer that affects mostly children and young adults. To augment the standard-of-care chemotherapy, we examined the possibility of protein-based therapy using mesenchymal stem cells (MSCs)-derived proteomes and OS-elevated proteins. While a conditioned medium (CM), collected from MSCs, did not present tumor-suppressing ability, the activation of PKA converted MSCs into induced tumor-suppressing cells (iTSCs). In a mouse model, the direct and hydrogel-assisted administration of CM inhibited tumor-induced bone destruction, and its effect was additive with cisplatin. CM was enriched with proteins such as calreticulin, which acted as an extracellular tumor suppressor by interacting with CD47. Notably, the level of

Indexed as

Bone NeoplasmsMesenchymal Stem CellsOsteosarcomaAnimalsCell Line, TumorGenes, Tumor SuppressorMicecalreticulincancer biologyCD47mouseMSCosteosarcomaPCOLCEproteome

Identifiers

PMID36943734
PMCPMC10030111
OpenAlexW4328049082

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read53
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.