Evidence map›Paper›PMID 32752099›Full record

ArticleInternational journal of molecular sciences2020

Induction of Apoptosis by Coptisine in Hep3B Hepatocellular Carcinoma Cells through Activation of the ROS-Mediated JNK Signaling Pathway.

So Young Kim, Hyun Hwangbo, Hyesook Lee, Cheol Park, Gi-Young Kim, Sung-Kwon Moon, Seok Joong Yun, Wun-Jae Kim, Jaehun Cheong, Yung Hyun Choi

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.8field-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

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Immunometabolic Targets in CD8Liver cancer · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Isoquinoline Alkaloids fromInternational journal of molecular sciences · 2022
    Article
  9. Review
  10. Review
  11. Article
  12. The Anticancer Effect of Natural Plant Alkaloid Isoquinolines.International journal of molecular sciences · 2021
    Review
  13. Article
  14. Article
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

10 authors at 5 institutions in 1 country.

So Young KimAnti-Aging Research Center, Dong-Eui University, Busan 47340, Korea.
Hyun HwangboAnti-Aging Research Center, Dong-Eui University, Busan 47340, Korea.
Hyesook LeeAnti-Aging Research Center, Dong-Eui University, Busan 47340, Korea.
Cheol ParkDivision of Basic Sciences, College of Liberal Studies, Dong-Eui University, Busan 47340, Korea.
Gi-Young KimDepartment of Marine Life Sciences, School of Marine Biomedical Sciences, Jeju National University, Jeju 63243, Korea.ORCID 0000-0002-6878-0790
Sung-Kwon MoonDepartment of Food and Nutrition, Chung-Ang University, Anseong 17546, Korea.
Seok Joong YunDepartment of Urology, College of Medicine, Chungbuk National University, Cheongju 28644, Korea.
Wun-Jae KimDepartment of Urology, College of Medicine, Chungbuk National University, Cheongju 28644, Korea.ORCID 0000-0002-8060-8926
Jaehun CheongDepartment of Molecular Biology, Pusan National University, Busan 46241, Korea.
Yung Hyun ChoiAnti-Aging Research Center, Dong-Eui University, Busan 47340, Korea.ORCID 0000-0002-1454-3124
Dong-Eui University · KRChungbuk National University · KRChung-Ang University · KRJeju National University · KRPusan National University · KR

Funding

Basic Science Research Program through the National Research Foundation of Korea grant funded by the Korea government 2018R1A2B2005705
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) has a high mortality rate worldwide, and treatment is very limited due to its high recurrence and low diagnosis rate, and therefore there is an increasing need to develop more effective drugs to treat HCC. Coptisine is one of the isoquinoline alkaloids, and it has various pharmacological effects. However, the evidence for the molecular mechanism of the anticancer efficacy is still insufficient. Therefore, this study investigated the antiproliferative effect of coptisine on human HCC Hep3B cells and identified the action mechanism. Our results showed that coptisine markedly increased DNA damage and apoptotic cell death, which was associated with induction of death receptor proteins. Coptisine also significantly upregulated expression of proapoptotic Bax protein, downregulated expression of anti-apoptotic Bcl-2 protein, and activated caspase-3, -8, and -9. In addition, coptisine remarkably increased the generation of reactive oxygen species (ROS), loss of mitochondrial membrane potential (MMP), and release of cytochrome

Indexed as

ApoptosisBerberineCarcinoma, HepatocellularCaspase 3Cell Line, TumorHumansJNK Mitogen-Activated Protein KinasesLiver NeoplasmsMAP Kinase Signaling SystemMembrane Potential, MitochondrialNeoplasm Recurrence, LocalProto-Oncogene Proteins c-bcl-2Reactive Oxygen SpeciesBCL2 protein, humanBerberineCASP3 protein, humanCaspase 3coptisineJNK Mitogen-Activated Protein KinasesProto-Oncogene Proteins c-bcl-2Reactive Oxygen Speciesapoptosisc-Jun N-terminal kinasecoptisineDNA damageHep3B cellsreactive oxygen species

Identifiers

PMID32752099
PMCPMC7432186
OpenAlexW3046930166

What Socratic 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 Socratic graph.