Evidence map›Paper›PMID 29780252›Full record

ArticleOncoTargets and therapy2018

Chelerythrine induced cell death through ROS-dependent ER stress in human prostate cancer cells.

Songjiang Wu, Yanying Yang, Feiping Li, Lifu Huang, Zihua Han, Guanfu Wang, Hongyuan Yu, Haiping Li

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2018. 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
1.7field-weighted citation impact, top 16% 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, 35 citations in OpenAlex.

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  4. Journal of Taibah University Medical Sciences · 2024
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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

8 authors at 2 institutions in 1 country.

Songjiang WuDepartment of Urology, Enze Hospital of Taizhou Enze Medical Center (Group), Taizhou, China.
Yanying YangDepartment of Urology, Enze Hospital of Taizhou Enze Medical Center (Group), Taizhou, China.
Feiping LiDepartment of Urology, Enze Hospital of Taizhou Enze Medical Center (Group), Taizhou, China.
Lifu HuangDepartment of Urology, Enze Hospital of Taizhou Enze Medical Center (Group), Taizhou, China.
Zihua HanDepartment of Urology, Enze Hospital of Taizhou Enze Medical Center (Group), Taizhou, China.
Guanfu WangDepartment of Urology, Enze Hospital of Taizhou Enze Medical Center (Group), Taizhou, China.
Hongyuan YuDepartment of Urology, Enze Hospital of Taizhou Enze Medical Center (Group), Taizhou, China.
Haiping LiDepartment of Urology, Enze Hospital of Taizhou Enze Medical Center (Group), Taizhou, China.
Wenzhou Medical University · CNZhejiang Taizhou Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionProstate cancer is the most common noncutaneous cancer and the second leading cause of cancer-related mortality worldwide and the third in USA in 2017. Chelerythrine (CHE), a naturalbenzo[c]phenanthridine alkaloid, formerly identified as a protein kinase C inhibitor, has also shown anticancer effect through a number of mechanisms. Herein, effect and mechanism of the CHE-induced apoptosis via reactive oxygen species (ROS)-mediated endoplasmic reticulum (ER) stress in prostate cancer cells were studied for the first time.

methodsIn our present study, we investigated whether CHE induced cell viability decrease, colony formation inhibition, and apoptosis in a dose-dependent manner in PC-3 cells. In addition, we showed that CHE increases intracellular ROS and leads to ROS-dependent ER stress and cell apoptosis.

resultsPre-treatment with N-acetyl cysteine, an ROS scavenger, totally reversed the CHE-induced cancer cell apoptosis as well as ER stress activation, suggesting that the ROS generation was responsible for the anticancer effects of CHE.

conclusionTaken together, our findings support one of the anticancer mechanisms by which CHE increased ROS accumulation in prostate cancer cells, thereby leading to ER stress and caused intrinsic apoptotic signaling. The study reveals that CHE could be a potential candidate for application in the treatment of prostate cancer.

Indexed as

apoptosischelerythrineendoplasmic reticulum stressprostate cancerreactive oxygen species

Identifiers

PMID29780252
PMCPMC5951218
OpenAlexW2802434259

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.