Evidence map›Paper›PMID 30545141›Full record

ArticleMolecules (Basel, Switzerland)2018

Atractylenolide II Induces Apoptosis of Prostate Cancer Cells through Regulation of AR and JAK2/STAT3 Signaling Pathways.

Jing Wang, Moussa Ide Nasser, Salah Adlat, Ming Ming Jiang, Nan Jiang, Li Gao

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

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  10. Two Novel Sesquiterpenoid Glycosides from the Rhizomes ofMolecules (Basel, Switzerland) · 2022
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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 2 institutions in 1 country.

Jing WangCollege of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, Heilongjiang, China. mingjingw@163.com.
Moussa Ide NasserColleges of Life Science and Technology, Dalian University, Dalian Economical Technological Development Zone, Dalian 116622, Liaoning, China. mingjing@dlu.edu.cn.ORCID 0000-0002-2670-6496
Salah AdlatColleges of Life Science and Technology, Dalian University, Dalian Economical Technological Development Zone, Dalian 116622, Liaoning, China. salahadlat86@gmail.com.ORCID 0000-0001-5318-8762
Ming Ming JiangCollege of Animal Science, Heilongjiang Agriculture Economics Vocational College, Mudanjiang 157041, Heilongjiang, China. mmingjiang81@163.com.
Nan JiangColleges of Life Science and Technology, Dalian University, Dalian Economical Technological Development Zone, Dalian 116622, Liaoning, China. jiangnan678@sohu.com.
Li GaoCollege of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, Heilongjiang, China. gaoli@neau.edu.cn.
Dalian University · CNNortheast Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate cancer is the most common illness affecting men worldwide. Although much progress has been made in the study of prostate cancer prevention and treatment, less attention has been paid to the molecular mechanism of the disease. The molecular arrangement by which atractylenolide II (ATR II) induces human prostate cancer cytotoxicity was comprehensively examined in the present study. As indicated by the results, ATR II could inhibit prostate cancer cell proliferation and promote DU145 and LNCaP cell apoptosis through induced G2/M cell cycle arrest. The cell apoptosis process induced by ATR II in both DU145 and LNCaP cells was associated with its ability to inhibit androgen receptor (AR) with overexpression of protein inhibitor of activated STAT-1 (PIAS1) and the repression of Janus kinase (Jak2) signaling pathways. The data from the present study demonstrated the antitumor effects and the potential pharmacological application of ATR II as an efficient drug for prostate cancer treatment.

Indexed as

Antineoplastic AgentsApoptosisCell Line, TumorHumansJanus Kinase 2LactonesMaleProstatic NeoplasmsReceptors, AndrogenSesquiterpenesSignal TransductionSTAT3 Transcription FactorAntineoplastic Agentsatractylenolide IIJAK2 protein, humanJanus Kinase 2LactonesReceptors, AndrogenSesquiterpenesSTAT3 protein, humanSTAT3 Transcription FactorapoptosisAR/PIAS1ATR IIG2/M arrestJAK2/STAT3

Identifiers

PMID30545141
PMCPMC6320989
OpenAlexW2903589599

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.