Evidence map›Paper›PMID 32751249›Full record

ArticleAntioxidants (Basel, Switzerland)2020

Saponin Formosanin C-induced Ferritinophagy and Ferroptosis in Human Hepatocellular Carcinoma Cells.

Pin-Lun Lin, Han-Hsuan Tang, Shan-Ying Wu, Ning-Sing Shaw, Chun-Li Su

Open access · goldAbstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
10.6field-weighted citation impact, top 1% 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

58 citing papers in PubMed, 125 citations in OpenAlex.

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  13. Recent progress of ferroptosis in cancers and drug discovery.Asian journal of pharmaceutical sciences · 2024
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  17. Ferroptosis and cuproptposis in kidney Diseases: dysfunction of cell metabolism.Apoptosis : an international journal on programmed cell death · 2024
    Review
  18. Article
  19. Ferritinophagy induced ferroptosis in the management of cancer.Cellular oncology (Dordrecht, Netherlands) · 2024
    Review
  20. Review
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

5 authors at 2 institutions in 1 country.

Pin-Lun LinDepartment of Human Development and Family Studies, National Taiwan Normal University, Taipei 106, Taiwan.ORCID 0000-0001-5313-7180
Han-Hsuan TangGraduate Program of Nutrition Science, School of Life Science, National Taiwan Normal University, Taipei 106, Taiwan.ORCID 0000-0002-9034-3597
Shan-Ying WuGraduate Program of Nutrition Science, School of Life Science, National Taiwan Normal University, Taipei 106, Taiwan.
Ning-Sing ShawDepartment of Biochemical Science and Technology, College of Life Science, National Taiwan University, Taipei 106, Taiwan.
Chun-Li SuDepartment of Human Development and Family Studies, National Taiwan Normal University, Taipei 106, Taiwan.ORCID 0000-0001-7617-2077
National Taiwan Normal University · TWNational Taiwan University · TW

Funding

Ministry of Science and Technology, Taiwan MOST 105-2320-B-003-003Ministry of Science and Technology, Taiwan MOST 105-2514-S-003-006Ministry of Science and Technology, Taiwan MOST 106-2320-B-003-006-MY3Ministry of Science and Technology, Taiwan MOST 106-2514-S-003-006National Taiwan Normal University 10502National Taiwan Normal University 10602
6 · The paper itself

Abstract

Ferroptosis, a recently discovered form of iron-dependent cell death, requires an increased level of lipid-reactive oxygen species (ROS). Ferritinophagy, a ferritin degradation pathway, depends on a selective autophagic cargo receptor (NCOA4). By screening various types of natural compounds, formosanin C (FC) was identified as a novel ferroptosis inducer, characterized by attenuations of FC-induced viability inhibition and lipid ROS formation in the presence of ferroptosis inhibitor. FC also induced autophagic flux, evidenced by preventing autophagic marker LC3-II degradation and increasing yellow LC3 puncta in tandem fluorescent-tagged LC3 (mRFP-GFP) reporter plasmid (ptfLC3) transfected cells when combined with autophagic flux inhibitor. It is noteworthy that FC-induced ferroptosis and autophagic flux were stronger in HepG2 cells expressing higher NCOA4 and lower ferritin heavy chain 1 (FTH1) levels, agreeing with the results of gene expression analysis using CTRP and PRISM, indicating that FTH1 expression level exhibited a significant negative correlation with the sensitivity of the cells to a ferroptosis inducer. Confocal and electron microscopy confirmed the pronounced involvement of ferritinophagy in FC-induced ferroptosis in the cells with elevated NCOA4. Since ferroptosis is a non-apoptotic form of cell death, our data suggest FC has chemotherapeutic potential against apoptosis-resistant HCC with a higher NCOA4 expression via ferritinophagy.

Indexed as

autophagyferritinophagyferroptosisformosanin Chepatocellular carcinoma

Identifiers

PMID32751249
PMCPMC7463707
OpenAlexW3045607520

What OpenQuestion holds

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LicenceCC BY
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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.