Evidence map›Paper›PMID 34054558›Full record

ArticleFrontiers in pharmacology2021

Min Jeong Kim, Jin Mo Ku, Se Hyang Hong, Hyo In Kim, Yun Young Kwon, Joon-Sang Park, Deok Hyun Jung, Yong Cheol Shin, Seong-Gyu Ko

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Frontiers in pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Herbal Combination ofFood science & nutrition · 2025
    Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Min Jeong KimDepartment of Science in Korean Medicine, Graduate School, Kyung Hee University, Seoul, South Korea.
Jin Mo KuDepartment of Preventive Medicine, College of Korean Medicine, Kyung Hee University, Seoul, South Korea.
Se Hyang HongDepartment of Preventive Medicine, College of Korean Medicine, Kyung Hee University, Seoul, South Korea.
Hyo In KimDepartment of Science in Korean Medicine, Graduate School, Kyung Hee University, Seoul, South Korea.
Yun Young KwonDepartment of Korean Medicine, College of Korean Medicine, Graduate School, Kyung Hee University, Seoul, South Korea.
Joon-Sang ParkDepartment of Korean Medicine, College of Korean Medicine, Graduate School, Kyung Hee University, Seoul, South Korea.
Deok Hyun JungDepartment of Korean Medicine, College of Korean Medicine, Graduate School, Kyung Hee University, Seoul, South Korea.
Yong Cheol ShinDepartment of Preventive Medicine, College of Korean Medicine, Kyung Hee University, Seoul, South Korea.
Seong-Gyu KoDepartment of Preventive Medicine, College of Korean Medicine, Kyung Hee University, Seoul, South Korea.
Kyung Hee University · KRHarvard University · USJeil Pharmaceutical (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate cancer is the second most commonly diagnosed cancer, and prostate cancer is the second most common cause of cancer death in United States men after lung cancer. Many therapies are used to treat prostate cancer, and chemotherapy is one of the most relevant treatments. However, chemotherapy has many side effects, and repeated administration of chemotherapeutic agents leads to acquired resistance. Thus, new drugs with few side effects are needed. We investigated the molecular mechanism of action of JI017 in human prostate cancer cells. We identified an endoplasmic reticulum (ER) stress pathway that depended on the reactive oxygen species (ROS) pathway and played a crucial role in JI017-induced apoptosis. We measured cell viability by the MTS assay to determine the effect of JI017. Analysis of apoptosis, mitochondrial dysfunction, and cell cycle features was performed by flow cytometry. We used western blot and RT-PCR to measure the levels of the proteins of the unfolded protein response (UPR) pathway and apoptosis markers. Immunoprecipitation assay and transfection were used to determine the expression levels of proteins interacting with the pathways influenced by JI017 in prostate cancer cells. The anticancer effects induced by JI017 were evaluated. JI017 induced cell death that regulated apoptotic molecules and caused cell cycle arrest that inhibited the proliferation of cancer cells. Moreover, JI017 generated ROS. Accumulation of ROS caused ER stress through the PERK-eIF2α-CHOP and IRE1α-CHOP pathways. Furthermore, persistent activation of the UPR pathway induced by JI017 treatment triggered mitochondrial dysfunction, including dissipation of mitochondrial membrane potential, which activated intrinsic apoptotic pathway in human prostate cancer cells. The data indicated that N-acetyl-L-cysteine diminished apoptosis. We demonstrated that JI017 induced ER stress and cell death. Anticancer properties of JI017 in prostate cancer cells and in a human prostate cancer model involved ROS-mediated ER stress. Thus, JI017 treatment provides a new strategy for chemotherapy of prostate cancer.

Indexed as

cancerCHOPer stressJI017mitochondria cell deathROS

Identifiers

PMID34054558
PMCPMC8155384
OpenAlexW3160808504

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.