Evidence map›Paper›PMID 30609256›Full record

ArticleJournal of cellular and molecular medicine2019

Oestrogen-related receptor alpha mediates chemotherapy resistance of osteosarcoma cells via regulation of ABCB1.

Yantao Chen, Kunshui Zhang, Yang Li, Ruilian Guo, Kelin Zhang, Guifang Zhong, Qing He

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 32 citations in OpenAlex.

  1. MiRNAs: main players of cancer drug resistance target ABC transporters.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    Review
  2. ALKBH3-regulated mActa pharmaceutica Sinica. B · 2025
    Article
  3. Review
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  6. Review
  7. Article
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  10. NTheranostics · 2022
    Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Theranostics · 2020
    Article
  18. 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

7 authors at 1 institution in 1 country.

Yantao ChenOrthopaedics Department, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Kunshui ZhangDepartment of Pharmacy, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Yang LiPediatric Hematology & Oncology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Ruilian GuoSICU Department, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Kelin ZhangSICU Department, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Guifang ZhongSICU Department, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Qing HeSICU Department, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.ORCID 0000-0002-9382-4847
Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemotherapy resistance is one of the major challenges for the treatment of osteosarcoma (OS). The potential roles of oestrogenic signals in the chemoresistance of OS cells were investigated. As compare to the parental cells, the doxorubicin and cisplatin (CDDP) resistant OS cells had greater levels of oestrogen-related receptors alpha (ERRα). Targeted inhibition of ERRα by its specific siRNAs or inverse agonist XCT-790 can restore the sensitivity of OS resistant cells to chemotherapy. This might be due to that si-ERRα can decrease the expression of P-glycoprotein (P-gp, encoded by ABCB1), one important ABC membrane transporter for drug efflux. XCT-790 can decrease the transcription and mRNA stability of ABCB1, while had no effect on protein stability of P-gp. ERRα can bind to the transcription factor of SP3 to increase the transcription of ABCB1. Furthermore, XCT-790 treatment decreased the expression of miR-9, which can bind to the 3'UTR of ABCB1 and trigger its decay. Collectively, we found that ERRα can regulate the chemoresistance of OS cells via regulating the transcription and mRNA stability of ABCB1. Targeted inhibition of ERRα might be a potential approach for OS therapy.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsATP Binding Cassette Transporter, Subfamily BBone NeoplasmsCell Line, TumorCell ProliferationCisplatinDoxorubicinDrug Resistance, NeoplasmERRalpha Estrogen-Related ReceptorGene Expression Regulation, NeoplasticHumansMicroRNAsNitrilesOsteosarcomaProtein BindingReceptors, EstrogenABCB1 protein, humanATP Binding Cassette Transporter, Subfamily BCisplatinDoxorubicinERRalpha Estrogen-Related ReceptorMicroRNAsMIRN92 microRNA, humanNitrilesReceptors, EstrogenSp3 Transcription FactorThiazolesXCT790ABCB1ERRαmiR-9osteosarcomaSP3

Identifiers

PMID30609256
PMCPMC6378180
OpenAlexW2908113424

What OpenQuestion holds

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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.