Evidence map›Paper›PMID 32882759›Full record

ArticleYonsei medical journal2020

Exosomal CircPRRX1 Enhances Doxorubicin Resistance in Gastric Cancer by Regulating MiR-3064-5p/PTPN14 Signaling.

Shumin Wang, Mei Ping, Bin Song, Yarong Guo, Yuanfei Li, Junmei Jia

Open access · goldAbstract read
In one paragraph

Article in Yonsei medical journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Review
  6. siRNA-based strategies to combat drug resistance in gastric cancer.Medical oncology (Northwood, London, England) · 2024
    Review
  7. Review
  8. miRNAs as short non-coding RNAs in regulating doxorubicin resistance.Journal of cell communication and signaling · 2023
    Review
  9. Article
  10. Article
  11. Review
  12. Tumor-derived exosomal non-coding RNAs as diagnostic biomarkers in cancer.Cellular and molecular life sciences : CMLS · 2022
    Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
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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

6 authors at 1 institution in 1 country.

Shumin WangDepartment of Oncology, First Hospital of Shanxi Medical University, Taiyuan City, Shanxi Province, China.ORCID https://orcid.org/0000-0003-0543-2331
Mei PingDepartment of Oncology, First Hospital of Shanxi Medical University, Taiyuan City, Shanxi Province, China.ORCID https://orcid.org/0000-0003-1339-4363
Bin SongDepartment of Oncology, First Hospital of Shanxi Medical University, Taiyuan City, Shanxi Province, China.ORCID https://orcid.org/0000-0002-0333-8379
Yarong GuoDepartment of Oncology, First Hospital of Shanxi Medical University, Taiyuan City, Shanxi Province, China.ORCID https://orcid.org/0000-0002-1506-546X
Yuanfei LiDepartment of Oncology, First Hospital of Shanxi Medical University, Taiyuan City, Shanxi Province, China.ORCID https://orcid.org/0000-0002-9219-6914
Junmei JiaDepartment of Oncology, First Hospital of Shanxi Medical University, Taiyuan City, Shanxi Province, China. iniawj@163.com.ORCID https://orcid.org/0000-0002-9835-0636
Shanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeGastric cancer (GC) is a malignant tumor with a high mortality rate. Drug resistance is a major obstacle to GC therapy. This study aimed to investigate the role and mechanism of exosomal circPRRX1 in doxorubicin resistance in GC. MATERIALS AND

methodsHGC-27 and AGS cells were exposed to different doses of doxorubicin to construct doxorubicin-resistant cell lines. Levels of circPRRX1, miR-3064-5p, and nonreceptor tyrosine phosphatase 14 (PTPN14) were detected by quantitative real-time PCR or Western blot assay. Then, 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide, transwell, and Western blot assays were used to explore the function of circPRRX1 in GC cells. Interactions among circPRRX1, miR-3064-5p, and PTPN14 were confirmed by dual-luciferase reporter assay. The in vivo function of circPRRX1 was analyzed in a xenograft tumor model.

resultsCircPRRX1 was highly expressed in doxorubicin-resistant GC cell lines. Knockdown of circPRRX1 reversed doxorubicin resistance in doxorubicin-resistant GC cells. Additionally, extracellular circPRRX1 was carried by exosomes to spread doxorubicin resistance. CircPRRX1 silencing reduced doxorubicin resistance by targeting miR-3064-5p or regulating PTPN14. In GC patients, high levels of circPRRX1 in serum exosomes were associated with poor responses to doxorubicin treatment. Moreover, depletion of circPRRX1 reduced doxorubicin resistance in vivo.

conclusionCircPRRX1 strengthened doxorubicin resistance by modulating miR-3064-5p/PTPN14 signaling and might be a therapeutic target for GC patients.

Indexed as

Cell Line, TumorDoxorubicinDrug Resistance, NeoplasmExosomesGene Expression Regulation, NeoplasticHomeodomain ProteinsHumansMicroRNAsProtein Tyrosine Phosphatases, Non-ReceptorReal-Time Polymerase Chain ReactionSignal TransductionStomach NeoplasmsDoxorubicinHomeodomain ProteinsMicroRNAsProtein Tyrosine Phosphatases, Non-ReceptorPRRX1 protein, humanPTPN14 protein, humanCircPRRX1DoxorubicinExosomeGastric cancerMiR-3064-5pPTPN14

Identifiers

PMID32882759
PMCPMC7471080
OpenAlexW3081773422

What OpenQuestion holds

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LicenceCC BY-NC
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.