Evidence map›Paper›PMID 30976078›Full record

ArticleScientific reports2019

Small-Molecule Ferroptotic Agents with Potential to Selectively Target Cancer Stem Cells.

William R Taylor, Sara R Fedorka, Ibtissam Gad, Ronit Shah, Hanan D Alqahtani, Radhika Koranne, Nishanth Kuganesan, Samkeliso Dlamini, Tim Rogers, Ayad Al-Hamashi and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

44 citing papers in PubMed, 68 citations in OpenAlex.

  1. Circular RNAs in ferroptosis regulation and tumor progression of gynecological and breast cancers: molecular mechanisms and therapeutic potential.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

16 authors at 3 institutions in 1 country.

William R TaylorDepartment of Biological Sciences, College of Natural Sciences and Mathematics, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio, 43606, United States. william.taylor3@utoledo.edu.
Sara R FedorkaDepartment of Medicinal and Biological Chemistry, College of Pharmacy and Pharmaceutical Sciences, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio, 43606, United States.
Ibtissam GadDepartment of Biological Sciences, College of Natural Sciences and Mathematics, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio, 43606, United States.
Ronit ShahDepartment of Biological Sciences, College of Natural Sciences and Mathematics, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio, 43606, United States.
Hanan D AlqahtaniDepartment of Biological Sciences, College of Natural Sciences and Mathematics, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio, 43606, United States.
Radhika KoranneDepartment of Biological Sciences, College of Natural Sciences and Mathematics, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio, 43606, United States.
Nishanth KuganesanDepartment of Biological Sciences, College of Natural Sciences and Mathematics, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio, 43606, United States.
Samkeliso DlaminiDepartment of Medicinal and Biological Chemistry, College of Pharmacy and Pharmaceutical Sciences, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio, 43606, United States.
Tim RogersDepartment of Biological Sciences, College of Natural Sciences and Mathematics, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio, 43606, United States.
Ayad Al-HamashiDepartment of Medicinal and Biological Chemistry, College of Pharmacy and Pharmaceutical Sciences, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio, 43606, United States.
Veronika KholodovychDepartment of Biological Sciences, College of Natural Sciences and Mathematics, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio, 43606, United States.
Yusuf BarudiDepartment of Biological Sciences, College of Natural Sciences and Mathematics, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio, 43606, United States.
Damian JunkDepartment of Pathology, Case Western Reserve University School of Medicine, Case Comprehensive Cancer Center, 2103 Cornell Road, WRB 3-134, Cleveland, Ohio, 44106, United States.
Maisha S RashidDepartment of Biological Sciences, College of Natural Sciences and Mathematics, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio, 43606, United States.
Mark W JacksonDepartment of Pathology, Case Western Reserve University School of Medicine, Case Comprehensive Cancer Center, 2103 Cornell Road, WRB 3-134, Cleveland, Ohio, 44106, United States.
L M Viranga TillekeratneDepartment of Medicinal and Biological Chemistry, College of Pharmacy and Pharmaceutical Sciences, The University of Toledo, 2801 W. Bancroft Street, Toledo, Ohio, 43606, United States. ltillek@utoledo.edu.
University of Toledo · USCornell University · USUniversity School · US

Funding

TELOMERASE INACTIVATION BY RNASE L SIGNALS CELL DEATHP01CA062220 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI LI, XIAOXIA, STARK, GEORGE ROBERT · 1994 to 2020
$35.6M
RESEARCH ONCOLOGY TRAINING GRANTT32CA059366 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI JACKSON, MARK W. · 1993 to 2025
$5.5M
Identification of a noval oncogene using validation-based insertional mutagenesisR01CA138421 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI JACKSON, MARK W. · 2010 to 2020
$3.2M
Novel Small Molecule Ferroptotic Compounds to Target Mesenchymal Breast Cancer and Breast Cancer Stem CellsR15CA213185 · NCI · UNIVERSITY OF TOLEDO · PI TILLEKERATNE, VIRANGA · 2018 to 2018
$449k
Regulation of the Mitotic Checkpoint by Gsk3R15GM120712 · NIGMS · UNIVERSITY OF TOLEDO · PI TAYLOR, WILLIAM R. · 2017 to 2017
$443k
Regulation of Sororin by Cdk1-mediated Phosphorylation.R15GM100440 · NIGMS · UNIVERSITY OF TOLEDO · PI TAYLOR, WILLIAM R. · 2012 to 2012
$291k
NCI NIH HHS P01 CA062220NCI NIH HHS R01 CA138421NCI NIH HHS R15 CA213185NCI NIH HHS T32 CA059366NIGMS NIH HHS R15 GM100440NIGMS NIH HHS R15 GM120712
6 · The paper itself

Abstract

Effective management of advanced cancer requires systemic treatment including small molecules that target unique features of aggressive tumor cells. At the same time, tumors are heterogeneous and current evidence suggests that a subpopulation of tumor cells, called tumor initiating or cancer stem cells, are responsible for metastatic dissemination, tumor relapse and possibly drug resistance. Classical apoptotic drugs are less effective against this critical subpopulation. In the course of generating a library of open-chain epothilones, we discovered a new class of small molecule anticancer agents that has no effect on tubulin but instead kills selected cancer cell lines by harnessing reactive oxygen species to induce ferroptosis. Interestingly, we find that drug sensitivity is highest in tumor cells with a mesenchymal phenotype. Furthermore, these compounds showed enhanced toxicity towards mesenchymal breast cancer populations with cancer stem cell properties in vitro. In summary, we have identified a new class of small molecule ferroptotic agents that warrant further investigation.

Indexed as

FerroptosisAntineoplastic AgentsCell ProliferationHumansMesodermNeoplasmsNeoplastic Stem CellsReactive Oxygen SpeciesSmall Molecule LibrariesTumor Cells, CulturedAntineoplastic AgentsReactive Oxygen SpeciesSmall Molecule Libraries

Identifiers

PMID30976078
PMCPMC6459861
OpenAlexW2939712878

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.