Evidence map›Paper›PMID 31269698›Full record

ArticleMolecules (Basel, Switzerland)2019

Licochalcone A Suppresses the Proliferation of Osteosarcoma Cells through Autophagy and ATM-Chk2 Activation.

Tai-Shan Shen, Yung-Ken Hsu, Yi-Fu Huang, Hsuan-Ying Chen, Cheng-Pu Hsieh, Chiu-Liang Chen

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Frontiers in microbiology · 2022
    Article
  12. Article
  13. Anti-Inflammatory Effect of Licochalcone A via Regulation of ORAI1 and KInternational journal of molecular sciences · 2021
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Antitumoral Properties of Natural Products.Molecules (Basel, Switzerland) · 2020
    Article
  19. Article
  20. Microbial Transformation of Licochalcones.Molecules (Basel, Switzerland) · 2019
    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

6 authors at 2 institutions in 1 country.

Tai-Shan ShenDepartment of Orthopedic Surgery, Changhua Christian Hospital, Changhua 50006, Taiwan.
Yung-Ken HsuDepartment of Orthopedic Surgery, Changhua Christian Hospital, Changhua 50006, Taiwan.
Yi-Fu HuangOrthopedics & Sports Medicine Laboratory, Changhua Christian Hospital, Changhua 50006, Taiwan.
Hsuan-Ying ChenOrthopedics & Sports Medicine Laboratory, Changhua Christian Hospital, Changhua 50006, Taiwan.
Cheng-Pu HsiehDepartment of Orthopedic Surgery, Changhua Christian Hospital, Changhua 50006, Taiwan.
Chiu-Liang ChenDepartment of Orthopedic Surgery, Changhua Christian Hospital, Changhua 50006, Taiwan. 111111@cch.org.tw.ORCID 0000-0001-6063-8821
Changhua Christian Hospital · TWDayeh University · TW

Funding

Changhua Christian Hospital Research Foundation 106-CCH-IRP-020
6 · The paper itself

Abstract

Licochalcone A, a flavonoid extracted from licorice root, has been shown to exhibit broad anti-inflammatory, anti-bacterial, anticancer, and antioxidative bioactivity. In this study, we investigated the antitumor activity of Licochalcone A against human osteosarcoma cell lines. The data showed that Licochalcone A significantly suppressed cell viability in MTT assay and colony formation assay in osteosarcoma cell lines. Exposure to Licochalcone A blocked cell cycle progression at the G2/M transition and induced extrinsic apoptotic pathway in osteosarcoma cell lines. Furthermore, we found the Licochalcone A exposure resulted in rapid ATM and Chk2 activation, and high levels of nuclear foci of phosphorylated Chk2 at Thr 68 site in osteosarcoma cell lines. In addition, Licochalcone A exposure significantly induced autophagy in osteosarcoma cell lines. When Licochalcone A-induced autophagy was blocked by the autophagy inhibitor chloroquine, the expression of activated caspase-3 and Annexin V positive cells were reduced, and cell viability was rescued in Licochalcone A-treated osteosarcoma cell lines. These data indicate that the activation of ATM-Chk2 checkpoint pathway and autophagy may contribute to Licochalcone A-induced anti-proliferating effect in osteosarcoma cell lines. Our findings display the possibility that Licochalcone A may serve as a potential therapeutic agent against osteosarcoma.

Indexed as

ApoptosisAtaxia Telangiectasia Mutated ProteinsAutophagyCell Cycle CheckpointsCell Line, TumorCell ProliferationCell SurvivalChalconesCheckpoint Kinase 2HumansOsteosarcomaAtaxia Telangiectasia Mutated ProteinsChalconesCheckpoint Kinase 2CHEK2 protein, humanlicochalcone AATM-Chk2autophagyLicochalcone Aosteosarcoma

Identifiers

PMID31269698
PMCPMC6651087
OpenAlexW2953903131

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.