Evidence map›Paper›PMID 22321380›Full record

ArticleToxicology in vitro : an international journal published in association with BIBRA2012

Hydroxyethyl disulfide as an efficient metabolic assay for cell viability in vitro.

Jie Li, Donglan Zhang, Kathleen M Ward, George C Prendergast, Iraimoudi S Ayene

Abstract read
In one paragraph

Article in Toxicology in vitro : an international journal published in association with BIBRA, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Wnt-C59 inhibits proinflammatory cytokine expression by reducing the interaction between β-catenin and NF-κB in LPS-stimulated epithelial and macrophage cells.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2021
    Article
  4. Comparison of specific expression profile in twoExperimental and therapeutic medicine · 2018
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

5 authors at 2 institutions in 1 country.

Jie LiLankenau Institute for Medical Research, 100 Lancaster Avenue, Wynnewood, PA 19096, USA.
Donglan Zhang
Kathleen M Ward
George C Prendergast
Iraimoudi S Ayene
Lankenau Institute for Medical Research · USThomas Jefferson University · US

Funding

Oxidative Pentose Cycle in Hypoxic Cancer Cell ResponseR01CA109604 · NCI · UNIVERSITY OF PENNSYLVANIA · PI AYENE, IRAIMOUDI S · 2005 to 2008
$988k
OPPC targeting to improve pancreatic cancer treatmentR03CA159315 · NCI · LANKENAU INSTITUTE FOR MEDICAL RESEARCH · PI PRENDERGAST, GEORGE C · 2012 to 2013
$160k
NCI NIH HHS CA-109604NCI NIH HHS R01 CA109604NCI NIH HHS R03 CA159315
6 · The paper itself

Abstract

Cell viability assays have a variety of well known practical and technical limitations. All the available approaches have disadvantages, such as non-linearity, high background and cumbersome protocols. Several commonly used tetrazolium chemicals rely upon generation of a colored formazan product formed by mitochondrial reduction of these compounds via phenazine methosulfate (PMS). However, sensitivity is inherently limited because their reduction relies on mitochondrial bioreduction and cellular transport of PMS, as well as accessibility to tetrazolium chemicals. In this study, we identify hydroxethyldisulfide (HEDS) as an inexpensive probe that can measure cellular metabolic activity without the need of PMS. In tissue culture medium, HEDS accurately quantitated metabolically active live cells in a linear manner superior to tetrazolium based and other assays. Cell toxicity produced by chemotherapeutics (cisplatin, etoposide), oxidants (hydrogen peroxide, acetaminophen), toxins (phenyl arsine oxide, arsenite) or ionizing radiation was rapidly determined by the HEDS assay. We found that HEDS was superior to other commonly used assays for cell viability determinations in its solubility, membrane permeability, and intracellular conversion to a metabolic reporter that is readily transported into the extracellular medium. Our findings establish the use of HEDS in a simple, rapid and low cost assay to accurately quantify viable cells.

Indexed as

Cell SurvivalAcetaminophenArsenicalsArsenitesBiological AssayCell Line, TumorCell ProliferationCisplatinDisulfidesEthanolEtoposideHumansHydrogen PeroxideHypoxiaRadiation, IonizingToxicity Tests2-hydroxyethyl disulfideAcetaminophenArsenicalsarseniteArsenitesCisplatinDisulfidesEthanolEtoposideHydrogen Peroxideoxophenylarsine

Identifiers

PMID22321380
PMCPMC3327773
OpenAlexW1983788003

What OpenQuestion holds

Textmetadata
LicenceTDM
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.