Evidence map›Paper›PMID 29460131›Full record

ArticleInternational urology and nephrology2018

Inhibiting autophagy overcomes docetaxel resistance in castration-resistant prostate cancer cells.

Quan Wang, Wei-Yang He, Yi-Zhou Zeng, Arman Hossain, Xin Gou

Open access · hybridAbstract read
In one paragraph

Article in International urology and nephrology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
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  3. Article
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  8. Pyrogallol fromInternational journal of molecular sciences · 2023
    Article
  9. Article
  10. Review
  11. Review
  12. Review
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  14. Review
  15. Article
  16. Review
  17. Resistance Mechanisms to Taxanes and PARP Inhibitors in Advanced Prostate Cancer.Current opinion in endocrine and metabolic research · 2020
    Article
  18. Review
  19. Review
  20. Prostate Cancer Energetics and Biosynthesis.Advances in experimental medicine and biology · 2019
    Review
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

5 authors at 2 institutions in 1 country.

Quan WangDepartment of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Wei-Yang HeDepartment of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Yi-Zhou ZengDepartment of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Arman HossainDepartment of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Xin GouDepartment of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China. gouxincq@163.com.
First Affiliated Hospital of Chongqing Medical University · CNChongqing Medical University · CN

Funding

the Municipal Health Bureau of Chongqing 2013-1-006the Natural Science Foundation of China 81372758the Natural Science Found Project of Chongqing cstc2013jcycA10058
6 · The paper itself

Abstract

backgroundThis study investigates the docetaxel-resistant mechanism and explores the effect of tea polyphenols (TP) on autophagy and its related mechanism in human castration-resistant prostate cancer (CRPC) cell lines PC3 and DU145.

methodsImmunofluorescence assay and annexin V-FITC/PI double staining flow cytometry were used to analyze the apoptosis and autophagy of PC3 and DU145 cells. The expression of autophagy-related proteins was detected by western bolt.

resultsDocetaxel could induce autophagy and apoptosis, together with the expression increase in p-JNK, p-Bcl-2 and Beclin1. The level of autophagy was remarkably decreased, but apoptosis was increased after combining with TP. In addition, the expression of p-mTOR was increased after combining with TP.

conclusionDocetaxel induces protective autophagy in CRPC cells by JNK pathway activation and then Bcl-2 phosphorylation and Beclin1 dissociation. TP activates mTOR pathway, which ultimately inhibits docetaxel-induced autophagy and improves therapeutic efficacy of docetaxel in CRPC cells.

Indexed as

Drug Resistance, NeoplasmAntineoplastic AgentsApoptosisAutophagyBeclin-1Cell Line, TumorDocetaxelHumansJNK Mitogen-Activated Protein KinasesMaleMAP Kinase Signaling SystemPhosphorylationPolyphenolsProstatic Neoplasms, Castration-ResistantProto-Oncogene Proteins c-bcl-2TaxoidsAntineoplastic AgentsBeclin-1BECN1 protein, humanDocetaxelJNK Mitogen-Activated Protein KinasesMTOR protein, humanPolyphenolsProto-Oncogene Proteins c-bcl-2TaxoidsTeaTOR Serine-Threonine KinasesAutophagyCastration-resistant prostate cancerDocetaxel resistanceTea polyphenol

Identifiers

PMID29460131
PMCPMC5878207
OpenAlexW2792844256

What OpenQuestion holds

Textmetadata
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.