Evidence map›Paper›PMID 41787040›Full record

ArticleDiscover oncology2026

S100A13 transcriptionally activated by SP1 facilitates osteosarcoma metastasis.

Fuxing Tang, Yisheng Wang, Tao Feng, Shuheng Zhou, Xianghong Zeng, Piwei Huang, Jinhui Peng, Bowei Liang

Abstract read
In one paragraph

Article in Discover oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Fuxing Tang *Department of Minimally Invasive Spine Surgery, Yulin Orthopaedics Hospital of Integrated Traditional Chinese and Western Medicine, Yulin, 537000, Guangxi, China.
Yisheng Wang *Department of Minimally Invasive Spine Surgery, Yulin Orthopaedics Hospital of Integrated Traditional Chinese and Western Medicine, Yulin, 537000, Guangxi, China.
Tao FengDepartment of Minimally Invasive Spine Surgery, Yulin Orthopaedics Hospital of Integrated Traditional Chinese and Western Medicine, Yulin, 537000, Guangxi, China.
Shuheng ZhouDepartment of Minimally Invasive Spine Surgery, Yulin Orthopaedics Hospital of Integrated Traditional Chinese and Western Medicine, Yulin, 537000, Guangxi, China.
Xianghong ZengDepartment of Minimally Invasive Spine Surgery, Yulin Orthopaedics Hospital of Integrated Traditional Chinese and Western Medicine, Yulin, 537000, Guangxi, China.
Piwei HuangDepartment of Spine Surgery, The Tenth Affiliated Hospital of Guangxi Medical University, Qinzhou, 535000, Guangxi, China. 497468187@qq.com.
Jinhui PengDepartment of Minimally Invasive Spine Surgery, Yulin Orthopaedics Hospital of Integrated Traditional Chinese and Western Medicine, Yulin, 537000, Guangxi, China. jimhooo@163.com.
Bowei LiangDepartment of Spine Surgery, The Sixth Affiliated Hospital of Guangxi Medical University, Yulin, 537000, Guangxi, China. 421339743@qq.com.

Funding

Yulin City Science Research and Technological Development Program 20247756
6 · The paper itself

Abstract

backgroundOsteosarcoma is a highly aggressive primary bone malignancy in which distant metastasis critically determines patient prognosis. However, the molecular drivers of metastasis remain incompletely understood, making the elucidation of these drivers a research priority.

methodsWe integrated single-cell and bulk RNA sequencing data to identify cell populations associated with metastasis and to screen for candidate therapeutic targets. Bioinformatics tools predicted upstream transcriptional regulators. Functional roles and transcriptional regulation were assessed via wound-healing, Transwell, and luciferase reporter assays.

resultsSingle-cell analysis of osteosarcoma heterogeneity identified the osteoblastic subcluster C2_OB as a major contributor to metastasis. cNMF analysis defined a metastasis-associated expression program (module 2) highly active in C2_OB, within which S100A13 emerged as a novel signature gene. S100A13 was overexpressed in osteosarcoma and correlated with metastasis and poor prognosis. Functional assays demonstrated that S100A13 promoted cell migration and invasion. Mechanistically, the transcription factor SP1 directly binds to the S100A13 promoter, activates its transcription, and thereby enhances the metastatic capacity of osteosarcoma cells.

conclusionThis study identifies S100A13 as a biomarker for osteosarcoma metastasis and poor prognosis, and delineates an SP1/S100A13 axis that drives metastatic progression.

Indexed as

MetastasisOsteosarcomaS100A13Single-cell RNA sequencingSP1

Identifiers

PMID41787040
PMCPMC13076697

What Socratic 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 Socratic graph.