Evidence map›Paper›PMID 27244886›Full record

ArticleOncotarget2016

Indolin-2-one compounds targeting thioredoxin reductase as potential anticancer drug leads.

Kamila K Kaminska, Helene C Bertrand, Hisashi Tajima, William C Stafford, Qing Cheng, Wan Chen, Geoffrey Wells, Elias S J Arner, Eng-Hui Chew

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

9 authors at 4 institutions in 4 countries.

Kamila K KaminskaDepartment of Pharmacy, Faculty of Science, National University of Singapore, S117543, Republic of Singapore.
Helene C BertrandUCL School of Pharmacy, University College London, London WC1N 1AX, United Kingdom.
Hisashi TajimaUCL School of Pharmacy, University College London, London WC1N 1AX, United Kingdom.
William C StaffordDivision of Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, SE-171 77, Stockholm, Sweden.
Qing ChengDivision of Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, SE-171 77, Stockholm, Sweden.
Wan ChenDepartment of Pharmacy, Faculty of Science, National University of Singapore, S117543, Republic of Singapore.
Geoffrey WellsUCL School of Pharmacy, University College London, London WC1N 1AX, United Kingdom.
Elias S J ArnerDivision of Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, SE-171 77, Stockholm, Sweden.
Eng-Hui ChewDepartment of Pharmacy, Faculty of Science, National University of Singapore, S117543, Republic of Singapore.
Karolinska Institutet · SENational University of Singapore · SGUniversity College London · GBCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several compounds bearing the indolinone chemical scaffold are known to possess anticancer properties. For example, the tyrosine kinase inhibitor sunitinib is an arylideneindolin-2-one compound. The chemical versatility associated with structural modifications of indolinone compounds underlies the potential to discover additional derivatives possessing anticancer properties. Previously synthesized 3-(2-oxoethylidene)indolin-2-one compounds, also known as supercinnamaldehyde (SCA) compounds in reference to the parent compound 1 [1-methyl-3(2-oxopropylidene)indolin-2-one], bear a nitrogen-linked α,β-unsaturated carbonyl (Michael acceptor) moiety. Here we found that analogs bearing N-substituents, in particular compound 4 and 5 carrying an N-butyl and N-benzyl substituent, respectively, were strongly cytotoxic towards human HCT 116 colorectal and MCF-7 breast carcinoma cells. These compounds also displayed strong thioredoxin reductase (TrxR) inhibitory activity that was likely attributed to the electrophilicity of the Michael acceptor moiety. Their selectivity towards cellular TrxR inhibition over related antioxidant enzymes glutathione reductase (GR), thioredoxin (Trx) and glutathione peroxidase (GPx) was mediated through targeting of the selenocysteine (Sec) residue in the highly accessible C-terminal active site of TrxR. TrxR inhibition mediated by indolin-2-one compounds led to cellular Trx oxidation, increased oxidative stress and activation of apoptosis signal-regulating kinase 1 (ASK1). These events also led to activation of p38 and JNK mitogen-activated protein kinase (MAPK) signaling pathways, and cell death with apoptotic features of PARP cleavage and caspase 3 activation. In conclusion, these results suggest that indolin-2-one-based compounds specifically targeting TrxR may serve as novel drug leads for anticancer therapy.

Indexed as

AnimalsAntineoplastic AgentsAntioxidantsCatalytic DomainCattleDrug DesignDrug Screening Assays, AntitumorFibroblastsGlutathione PeroxidaseGlutathione ReductaseHCT116 CellsHumansIndolesInhibitory Concentration 50MCF-7 CellsMiceAntineoplastic AgentsAntioxidantsGlutathione PeroxidaseGlutathione ReductaseIndolesindolin-2-onejugloneNaphthoquinonesReactive Oxygen SpeciesRecombinant ProteinsSelenocysteineThioredoxin-Disulfide ReductaseThioredoxinsTXN protein, humananticancerindolin-2-oneselenocysteinesupercinnamaldehydethioredoxin reductase

Identifiers

PMID27244886
PMCPMC5130005
OpenAlexW2401994137

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.