Evidence map›Paper›PMID 36536381›Full record

ArticleBMC medical genomics2022

Transcriptomics and metabolomics reveal changes in the regulatory mechanisms of osteosarcoma under different culture methods in vitro.

Sen Yang, Zhi Tian, Yi Feng, Kun Zhang, Yongchun Pan, Yuan Li, Zhichao Wang, Wenhao Wei, Xiaochen Qiao, Ruhao Zhou and 6 more

Open access · goldAbstract read
In one paragraph

Article in BMC medical genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 10 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

16 authors at 3 institutions in 1 country.

Sen Yang *Second Clinical Medical College, Shanxi Medical University, 382 Wuyi Road, Shanxi, 030001, Taiyuan, People's Republic of China.
Zhi Tian *Second Clinical Medical College, Shanxi Medical University, 382 Wuyi Road, Shanxi, 030001, Taiyuan, People's Republic of China.
Yi Feng *Second Clinical Medical College, Shanxi Medical University, 382 Wuyi Road, Shanxi, 030001, Taiyuan, People's Republic of China.
Kun ZhangSecond Clinical Medical College, Shanxi Medical University, 382 Wuyi Road, Shanxi, 030001, Taiyuan, People's Republic of China.
Yongchun PanDepartment of Orthopedics, The Third people's Hospital of Datong City, Shanxi, 037006, Datong, People's Republic of China.
Yuan LiSecond Clinical Medical College, Shanxi Medical University, 382 Wuyi Road, Shanxi, 030001, Taiyuan, People's Republic of China.
Zhichao WangShanxi Bethune Hospital, Third Hospital of Shanxi Medical University, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, 030032, Taiyuan, People's Republic of China.
Wenhao WeiSecond Clinical Medical College, Shanxi Medical University, 382 Wuyi Road, Shanxi, 030001, Taiyuan, People's Republic of China.
Xiaochen QiaoSecond Clinical Medical College, Shanxi Medical University, 382 Wuyi Road, Shanxi, 030001, Taiyuan, People's Republic of China.
Ruhao ZhouSecond Clinical Medical College, Shanxi Medical University, 382 Wuyi Road, Shanxi, 030001, Taiyuan, People's Republic of China.
Lei YanSecond Clinical Medical College, Shanxi Medical University, 382 Wuyi Road, Shanxi, 030001, Taiyuan, People's Republic of China.
Qian LiSecond Clinical Medical College, Shanxi Medical University, 382 Wuyi Road, Shanxi, 030001, Taiyuan, People's Republic of China.
Hua GuoSecond Clinical Medical College, Shanxi Medical University, 382 Wuyi Road, Shanxi, 030001, Taiyuan, People's Republic of China.
Jie YuanSecond Clinical Medical College, Shanxi Medical University, 382 Wuyi Road, Shanxi, 030001, Taiyuan, People's Republic of China.
Pengcui LiSecond Clinical Medical College, Shanxi Medical University, 382 Wuyi Road, Shanxi, 030001, Taiyuan, People's Republic of China.
Zhi LvSecond Clinical Medical College, Shanxi Medical University, 382 Wuyi Road, Shanxi, 030001, Taiyuan, People's Republic of China. zhilv2013@163.com.
Second Hospital of Shanxi Medical University · CNShanxi Medical University · CNShanxi Datong University · CN

Funding

Natural Science Foundation of Shanxi Province 201901D111373Natural Science Foundation of Shanxi Province 201903D321156Natural Science Foundation of Shanxi Province 20210302124410The National Natural Science Foundation of China 81772867The Second Hospital of Shanxi Medical University, four research fund projects within the hospital 2020001-10
6 · The paper itself

Abstract

backgroundRecently, increasing attention has been drawn to the impact of the tumor microenvironment (TME) on the occurrence and progression of malignant tumors. A variety of 3D culture techniques have been used to simulate TME in vitro. The purpose of this study was to reveal the differences in transcriptional and metabolic levels between osteosarcoma (OS) 2D cells, 3D cells, 3D cell-printed tissue, isolated tissue, and transplanted tumor tissue in vivo.

methodsWe cultured the OS Saos-2 cell line under different culture methods as 2D cells, 3D cells, 3D cell-printed tissue and isolated tissue for 14 days and transplanted tumors in vivo as a control group. Through transcriptomic and metabonomic analyses, we determined the changes in gene expression and metabolites in OS tissues under different culture methods.

resultsAt the transcriptional level, 166 differentially expressed genes were found, including the SMAD family, ID family, BMP family and other related genes, and they were enriched in the TGF-β signaling pathway, complement and coagulation cascades, signaling pathways regulating pluripotency of stem cells, Hippo signaling pathway, ferroptosis, cGMP-PKG signaling pathway and other pathways. At the metabolic level, 362 metabolites were significantly changed and enriched in metabolic pathways such as the Fc Epsilon RI signaling pathway, histidine metabolism, primary bile acid biosynthesis, steroid biosynthesis, protein digestion and absorption, ferroptosis, and arachidonic acid metabolism. After integrating the transcriptome and metabolomics data, it was found that 44 metabolic pathways were changed, and the significantly enriched pathways were ferroptosis and pyrimidine metabolism.

conclusionDifferent culture methods affect the gene expression and metabolite generation of OS Saos-2 cells. Moreover, the cell and tissue culture method in vitro cannot completely simulate TME in vivo, and the ferroptosis and pyrimidine metabolism pathways mediate the functional changes of OS Saos-2 cells in different microenvironments.

Indexed as

Bone NeoplasmsOsteosarcomaCulture TechniquesHumansPyrimidinesTranscriptomeTumor MicroenvironmentPyrimidinesMetabolomicsOsteosarcomaTranscriptomicsTumor microenvironment

Identifiers

PMID36536381
PMCPMC9762085
OpenAlexW4312113604

What OpenQuestion holds

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LicenceCC BY
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.