Evidence map›Paper›PMID 41522513›Full record

ArticlePeerJ2026

Cholesterol and steroid synthesis pathways may be involved in the inhibition of osteosarcoma cell viability by calcium-sensing receptor antagonism.

Luchuan Wang, Jianfa Wang, Xinjie Chu, Yao Liu, Yanping Fan, Xunzhong Qi, Jin Guo, Shuqiu Wang

Abstract read
In one paragraph

Article in PeerJ, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Luchuan WangDepartment of Pathophysiology, School of Basic Medicine, Jiamusi University, Jiamusi, China.
Jianfa WangDepartment of Orthopedics, School of Clinical Medicine, Jiamusi University, Jiamusi, China.
Xinjie ChuDepartment of Orthopedics, School of Clinical Medicine, Jiamusi University, Jiamusi, China.
Yao LiuDepartment of Pathophysiology, School of Basic Medicine, Jiamusi University, Jiamusi, China.
Yanping FanSchool of Rehabilitation, Jiamusi University, Jiamusi, China.
Xunzhong QiDepartment of Neurology, School of Clinical Medicine, Jiamusi University, Jiamusi, China.
Jin GuoSchool of Rehabilitation, Jiamusi University, Jiamusi, China.
Shuqiu WangDepartment of Pathophysiology, School of Basic Medicine, Jiamusi University, Jiamusi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: This study examined the effect of calcium-sensing receptor (CaSR) antagonism on human osteosarcoma cells and investigated the underlying molecular mechanisms of this effect through transcriptome sequencing. Methods: Human osteosarcoma cell lines MG-63 and Saos-2 were treated with different concentrations (0.1-10 µM) of the CaSR antagonist NPS-2143. Cell Counting Kit-8 (CCK-8) assays were used to detect the effect of CaSR antagonism on the viability of the cells. RNA sequencing was performed on cells treated with five µM NPS-2143 for 24 hours, followed by bioinformatic analysis to identify differentially expressed genes and enriched pathways. qRT-PCR was conducted to validate key genes. Results: CCK-8 assays showed that at low concentrations (0.1 and one µM), NPS-2143 had no significant effect on MG-63 and Saos-2 cell viability. At higher concentrations (five µM and 10 µM), the viability of MG-63 and Saos-2 cells was significantly reduced. Five µM was therefore selected for subsequent experiments. RNA sequencing revealed distinct gene expression profiles in NPS-2143-treated cells compared to controls. A total of 927 differentially expressed genes (DEGs) were identified in Saos-2 cells (378 upregulated, 549 downregulated), and 59 DEGs were identified in MG-63 cells (33 upregulated, 26 downregulated). Reactome and KEGG pathway enrichment analyses indicated significant enrichment of cholesterol and steroid biosynthesis-related pathways. Transcriptome sequencing showed that NPS-2143 modulated the expression of genes in cholesterol and steroid synthesis pathways. Real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) confirmed that NPS-2143 promoted the expression of the cholesterol and steroid synthesis pathway genes, Discussion: The inhibitory effect of NPS-2143 on MG-63 and Saos-2 osteosarcoma tumor cell viability was confirmed. CaSR antagonism significantly up-regulated genes involved in cholesterol and steroid biosynthesis, including

Indexed as

Bone NeoplasmsCholesterolNaphthalenesOsteosarcomaReceptors, Calcium-SensingSteroidsCell Line, TumorCell SurvivalGene Expression Regulation, NeoplasticHumansCASR protein, humanCholesterolN-(2-hydroxy-3-(2-cyano-3-chlorophenoxy)propyl)-1,1-dimethyl-2-(2-nephthyl)ethylamineNaphthalenesReceptors, Calcium-SensingSteroidsCaSR antagonistCholesterol synthesisNPS-2143OsteosarcomaTranscriptome sequencing

Identifiers

PMID41522513
PMCPMC12782028

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.