Evidence map›Paper›PMID 40045162›Full record

ArticleJournal of cellular and molecular medicine2025

Prognostic and Therapeutic Significance of Cancer-Associated Fibroblasts Genes in Osteosarcoma Based on Bulk and Single-Cell RNA Sequencing Data.

Yukang Que, Tianming Ding, Huming Wang, Shenglin Xu, Peng He, Qiling Shen, Kun Cao, Yang Luo, Yong Hu

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

9 authors.

Yukang QueDepartment of Orthopedics, The First Affiliated Hospital Anhui Medical University, Hefei, Anhui, China.ORCID 0009-0000-3845-2510
Tianming DingDepartment of Orthopedics, Yangzhou East Hospital, Yangzhou, Jiangsu, China.
Huming WangDepartment of Orthopedics, The First Affiliated Hospital Anhui Medical University, Hefei, Anhui, China.
Shenglin XuDepartment of Orthopedics, The First Affiliated Hospital Anhui Medical University, Hefei, Anhui, China.
Peng HeDepartment of Orthopedics, The First Affiliated Hospital Anhui Medical University, Hefei, Anhui, China.
Qiling ShenDepartment of Orthopedics, The First Affiliated Hospital Anhui Medical University, Hefei, Anhui, China.
Kun CaoDepartment of Orthopedics, The First Affiliated Hospital Anhui Medical University, Hefei, Anhui, China.
Yang LuoDepartment of Orthopedics, The First Affiliated Hospital Anhui Medical University, Hefei, Anhui, China.
Yong HuDepartment of Orthopedics, The First Affiliated Hospital Anhui Medical University, Hefei, Anhui, China.

Funding

Major scientific research projects of the Health Commission of Anhui Province AHWJ2023A10008Program for Upgrading Basic and Clinical Collaborative Research of Anhui Medical University 2023xkjT031Research Fund of Anhui Institute of Translational Medicine 2022zhyx-C34
6 · The paper itself

Abstract

Osteosarcoma (OS) is the most frequent primary solid malignancy of bone, whose course is usually dismal without efficient treatments. The aim of the study was to discover novel risk models to more accurately predict and improve the prognosis of patients with osteosarcoma. The single-cell RNA sequencing (scRNA-seq) data was obtained from the GEO database. Bulk RNA-seq data and microarray data of OS were obtained from the TARGET and GEO databases respectively. A clustering tree was plotted to classify all cells into different clusters. The "cellchat" R package was used to establish and visualise cell-cell interaction networks. Then Univariate COX regression analysis was used to determine the prognostic CAF-related genes, followed by the Lasso-Cox regression analysis to build a risk on the prognostic CAF-related genes. Finally, from multiple perspectives, the signature was validated as an accurate and dependable tool in predicting the prognosis and guiding treatment therapies in OS patients. From the single-cell dataset, six OS patients and 46,544 cells were enrolled. All cells were classified into 22 clusters, and the clusters were annotated to 14 types of cells. Subsequently, CAFs were observed as a vital TME components. In cell-cell interaction networks in OS cells, CAFs had a profound impact as four roles. Via the Univariate COX regression analysis, 14 CAF-related genes were screened out. By the Lasso-Cox regression analyses, 11 key CAF-related genes were obtained, based on which an 11-gene signature that could predict the prognosis of osteosarcoma patients was constructed. According to the median of risk scores, all patients were grouped in to the high- and low-risk group, and their overall survival, activated pathways, immune cell infiltrations, and drug sensitivity were significantly differential, which may have important implications for the clinical treatment of patients with osteosarcoma. Our study, a systematic analysis of gene and regulatory genes, has proven that CAF-related genes had excellent diagnostic and prognostic capabilities in OS, and it may reshape the TME in OS. The novel CAF-related risk signature can effectively predict the prognosis of OS and provide new strategies for cancer treatment.

Indexed as

Biomarkers, TumorBone NeoplasmsCancer-Associated FibroblastsOsteosarcomaSingle-Cell AnalysisFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansMalePrognosisSequence Analysis, RNATumor MicroenvironmentBiomarkers, Tumorcancer‐associated fibroblastsgenesosteosarcomaprognosissingle‐cell RNA sequencing

Identifiers

PMID40045162
PMCPMC11882394

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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.