Evidence map›Paper›PMID 42152486›Full record

ArticleBioMed research international2026

Celastrol Enhanced Doxorubicin-Mediated Apoptosis in Saos-2 Osteosarcoma Cells.

Fatemeh Pilevar, Dariush Shanehbandi, Amir Valizadeh, Leila Alem, Mehran Molavand, Maryam Majidinia, Bahman Yousefi, Elahe Mohammadian

Abstract read
In one paragraph

Article in BioMed research international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Fatemeh PilevarDepartment of Biochemistry, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran, tbzmed.ac.ir.ORCID https://orcid.org/0009-0000-4264-1285
Dariush ShanehbandiImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran, tbzmed.ac.ir.ORCID https://orcid.org/0000-0002-9449-0607
Amir ValizadehStudent Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran, tbzmed.ac.ir.ORCID https://orcid.org/0000-0002-7852-8118
Leila AlemDepartment of Biochemistry, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran, tbzmed.ac.ir.ORCID https://orcid.org/0000-0002-1903-9517
Mehran MolavandDepartment of Biochemistry, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran, tbzmed.ac.ir.ORCID https://orcid.org/0009-0007-3923-7549
Maryam MajidiniaSolid Tumor Research Center, Urmia University of Medical Sciences, Urmia, Iran, umsu.ac.ir.ORCID https://orcid.org/0000-0001-9776-5816
Bahman YousefiDepartment of Biochemistry, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran, tbzmed.ac.ir.ORCID https://orcid.org/0000-0002-4220-1527
Elahe MohammadianHealth Science Faculty, Nursing Department, Bahçeşehir Cyprus University Alayköy Campus, Mersin 10, Turkey.ORCID https://orcid.org/0009-0000-5287-8059

Funding

Tabriz University of Medical Sciences
6 · The paper itself

Abstract

backgroundOsteosarcoma is one of the most lethal types of human malignancy in the world. Natural compounds found in certain plant foods are considered chemotherapeutic agents that exert their effects through antiproliferative, proapoptotic, and pro-oxidant properties associated with cancer.

objectiveIn this study, we investigated the effects of celastrol on the doxorubicin-mediated apoptosis in osteosarcoma cells. Saso-2 cancer cells were treated with ascending concentrations of doxorubicin and celastrol alone or in combination.

methodsCytotoxicity was measured using the MTT assay. Flow cytometry with Annexin V-FITC/PI double staining was performed to quantify apoptotic cell populations. Western blot and quantitative reverse transcription-polymerase chain reaction (qRT-PCR) were used to measure the protein and mRNA expression levels of apoptosis mediators. An ELISA kit measured apoptosis.

resultIn Saos-2 cells, celastrol enhanced the cytotoxic effects of doxorubicin. A combination of doxorubicin and celastrol had a more potent effect on apoptosis induction and modulation of mRNA and protein levels of key apoptotic mediators, including Bax, Bcl-2, caspase-3, cytochrome c, and p53.

conclusionOverall, this study revealed that doxorubicin and celastrol could significantly potentiate doxorubicin-mediated apoptosis in osteosarcoma cells.

Indexed as

ApoptosisBone NeoplasmsDoxorubicinOsteosarcomaTriterpenesCell Line, TumorCell ProliferationCytochromes cDrug SynergismGene Expression Regulation, NeoplasticHumansPentacyclic TriterpenescelastrolCytochromes cDoxorubicinPentacyclic TriterpenesTriterpenesapoptosiscelastroldoxorubicinosteosarcoma

Identifiers

PMID42152486
PMCPMC13184160

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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 OpenQuestion graph.