Evidence map›Paper›PMID 33302580›Full record

ArticleAntioxidants (Basel, Switzerland)2020

Inhibition of NADPH Oxidases Activity by Diphenyleneiodonium Chloride as a Mechanism of Senescence Induction in Human Cancer Cells.

Katarzyna Piszczatowska, Dorota Przybylska, Ewa Sikora, Grażyna Mosieniak

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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 26 citations in OpenAlex.

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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 1 institution in 1 country.

Katarzyna PiszczatowskaLaboratory of Molecular Bases of Aging, Nencki Institute of Experimental Biology of Polish Academy of Sciences, Pasteura 3 St., 02-093 Warsaw, Poland.ORCID 0000-0002-6365-8382
Dorota PrzybylskaLaboratory of Molecular Bases of Aging, Nencki Institute of Experimental Biology of Polish Academy of Sciences, Pasteura 3 St., 02-093 Warsaw, Poland.
Ewa SikoraLaboratory of Molecular Bases of Aging, Nencki Institute of Experimental Biology of Polish Academy of Sciences, Pasteura 3 St., 02-093 Warsaw, Poland.
Grażyna MosieniakLaboratory of Molecular Bases of Aging, Nencki Institute of Experimental Biology of Polish Academy of Sciences, Pasteura 3 St., 02-093 Warsaw, Poland.ORCID 0000-0001-7957-1241
Instytut Biologii Doświadczalnej im. Marcelego Nenckiego · PL

Funding

National Science Center UMO-2014/15/B/NZ3/01150
6 · The paper itself

Abstract

NADPH oxidases (NOX) are commonly expressed ROS-producing enzymes that participate in the regulation of many signaling pathways, which influence cell metabolism, survival, and proliferation. Due to their high expression in several different types of cancer it was postulated that NOX promote tumor progression, growth, and survival. Thus, the inhibition of NOX activity was considered to have therapeutic potential. One of the possible outcomes of anticancer therapy, which has recently gained much interest, is cancer cell senescence. The induction of senescence leads to prolonged inhibition of proliferation and contributes to tumor growth restriction. The aim of our studies was to investigate the influence of low, non-toxic doses of diphenyleneiodonium chloride (DPI), a potent inhibitor of flavoenzymes including NADPH oxidases, on p53-proficient and p53-deficient HCT116 human colon cancer cells and MCF-7 breast cancer cells. We demonstrated that the temporal treatment of HCT116 and MCF-7 cancer cells (both p53 wild-type) with DPI caused induction of senescence, that was correlated with decreased level of ROS and upregulation of p53/p21 proteins. On the contrary, in the case of p53-/- HCT116 cells, apoptosis was shown to be the prevailing effect of DPI treatment. Thus, our studies provided a proof that inhibiting ROS production, and by this means influencing ROS sensitive pathways, remains an alternative strategy to facilitate so called therapy-induced senescence in cancers.

Indexed as

apoptosiscancerDPINADPH oxidasesROSsenescence

Identifiers

PMID33302580
PMCPMC7764543
OpenAlexW3112562422

What OpenQuestion holds

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Registered trials

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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.