Evidence map›Paper›PMID 32741371›Full record

ArticleJournal of experimental & clinical cancer research : CR2020

Genipin suppression of growth and metastasis in hepatocellular carcinoma through blocking activation of STAT-3.

Ming Hong, Selena Lee, Jacob Clayton, Wildman Yake, Jinke Li

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2020. 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 It has been retracted, and should not be counted.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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. A Pilot Study to Evaluate Genipin inInternational journal of molecular sciences · 2023
    Article
  4. Article
  5. Review
  6. Review
  7. Genipin in an Ex Vivo Corneal Model of Bacterial and Fungal Keratitis.Translational vision science & technology · 2021
    Article
  8. Article
  9. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Ming HongScience and Technology Innovation Center, Guangzhou University of Chinese Medicine, Guangzhou, China. hongming1986@gzucm.edu.cn.
Selena LeeDepartment of Pharmacology & Toxicology, University of Kansas, Lawrence, KS, USA.
Jacob ClaytonDepartment of Pharmacology & Toxicology, University of Kansas, Lawrence, KS, USA.
Wildman YakeDepartment of Pharmacology & Toxicology, University of Kansas, Lawrence, KS, USA.
Jinke LiDepartment of Pharmacology & Toxicology, University of Kansas, Lawrence, KS, USA. j086l791@ku.edu.
University of Kansas · USGuangzhou University of Chinese Medicine · CN

Funding

CSPG receptors and PTEN in CNS regenerationR01NS079432 · NINDS · TEMPLE UNIV OF THE COMMONWEALTH · PI LI, SHUXIN · 2014 to 2018
$1.7M
Funding from National Institutes of Health grants NS79432NINDS NIH HHS R01 NS079432Xing-lin Foundation of Guangzhou University of Chinese Medicine (GZF-1366732K)
6 · The paper itself

Abstract

backgroundThe signal transducer and activator of transcription-3 (STAT-3) can facilitate cancer progression and metastasis by being constitutively active via various signaling. Abundant evidence has indicated that STAT-3 may be a promising molecular target for cancer treatment.

methodsIn this study, a dual-luciferase assay-based screening of 537 compounds for STAT-3 inhibitors of hepatocellular carcinoma (HCC) cells was conducted, leading to the identification of genipin. Effects of genipin on HCC were assessed in a patient-derived xenograft nude mice model. Western blotting assay, chromatin immunoprecipitation (ChIP) assay, molecular docking study, tube formation assay, three-dimensional top culture assay, histological examination, and immunofluorescence were utilized to evaluate the regulatory signaling pathway.

resultsOur research demonstrated that genipin suppresses STAT-3 phosphorylation and nuclear translocation, which may be attributed to the binding capacity of this compound to the Src homology-2 (SH2) domain of STAT-3. In addition, the therapeutic effects of genipin in a patient-derived HCC xenograft nude mice model were also demonstrated.

conclusionsIn conclusion, genipin showed therapeutic potential for HCC treatment by interacting with the SH2-STAT-3 domain and suppressing the activity of STAT-3. In the future, further research is planned to explore the potential role of genipin in combination with chemotherapy or radiotherapy for HCC.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsApoptosisBiomarkers, TumorCarcinoma, HepatocellularCell MovementCell ProliferationCholagogues and CholereticsEpithelial-Mesenchymal TransitionFemaleHumansIridoidsLiver NeoplasmsMiceMice, Inbred BALB CMice, NudeBiomarkers, TumorCholagogues and CholereticsgenipinIridoidsSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID32741371
PMCPMC7397684
OpenAlexW3046868863

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.