Evidence map›Paper›PMID 25096914›Full record

ArticleInternational journal of oncology2014

Auranofin displays anticancer activity against ovarian cancer cells through FOXO3 activation independent of p53.

See-Hyoung Park, Jung Han Lee, Jonathan S Berek, Mickey C-T Hu

Open access · bronzeAbstract read
In one paragraph

Article in International journal of oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

45 citing papers in PubMed, 100 citations in OpenAlex.

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  7. Arsenic exposure and increasedRedox biochemistry and chemistry · 2023
    Article
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  9. Evaluation of Auranofin Loading within Ferritin Nanocages.International journal of molecular sciences · 2022
    Article
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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

4 authors at 2 institutions in 2 countries.

See-Hyoung ParkDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Jung Han LeeDepartment of Obstetrics and Gynecology, Hanyang University School of Medicine, Seoul 133-792, Republic of Korea.
Jonathan S BerekDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Mickey C-T HuDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Stanford University · USHanyang University · KR

Funding

The Role of Regulation of FOXO3a in Tumor SuppressionR01CA113859 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HU, MICKEY C-T · 2006 to 2010
$1.2M
NCI NIH HHS R01 CA113859
6 · The paper itself

Abstract

Auranofin is a gold-containing compound classified by the World Health Organization as a clinically established rheumatoid arthritis therapeutic agent. Through drug screening for novel anticancer therapeutics, we unexpectedly identified auranofin as a potent anticancer agent against a p53-null ovarian carcinoma SKOV3 cell line. However, the molecular mechanism underlying auranofin-mediated anticancer activity in ovarian cancer cells is basically unknown. Here, we show that auranofin inhibits proliferation and survival of SKOV3 cells in a dose‑ and time‑dependent manner. Auranofin treatment activates the pro-apoptotic caspase-3, increases protein levels of apoptosis-inducing proteins Bax and Bim and reduces the expression of the anti-apoptotic mediator Bcl-2 in SKOV3 cells. Moreover, auranofin downregulates IκB kinase (IKK)-β and promotes nuclear localization and the activation of FOXO3 tumor suppressor, leading to cellular apoptosis in SKOV3 cells. In contrast, silencing FOXO3 diminishes the pro-apoptotic signaling of auranofin in SKOV3 cells. These results suggest that auranofin may induce caspase-3-mediated apoptosis in a FOXO3-dependent manner. The observed upregulation of pro-apoptotic genes and apoptosis in cancer cells without p53 in response to auranofin suggests a novel p53-independent mechanism underlying auranofin-induced apoptosis in ovarian cancer cells.

Indexed as

Antineoplastic AgentsApoptosisApoptosis Regulatory ProteinsAuranofinCell Line, TumorCell NucleusCell ProliferationFemaleForkhead Box Protein O3Forkhead Transcription FactorsGene Expression Regulation, NeoplasticHumansOvarian NeoplasmsTumor Suppressor Protein p53Antineoplastic AgentsApoptosis Regulatory ProteinsAuranofinForkhead Box Protein O3Forkhead Transcription FactorsFOXO3 protein, humanTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID25096914
PMCPMC4151813
OpenAlexW1968922576

What OpenQuestion holds

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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.