Evidence map›Paper›PMID 36619644›Full record

ArticleFrontiers in medicine2022

Bortezomib is an effective enhancer for chemical probe-dependent superoxide detection.

Misaki Matsumoto, Hikari Sawada, Kazumi Iwata, Masakazu Ibi, Nozomi Asaoka, Masato Katsuyama, Kaori Shintani-Ishida, Hiroshi Ikegaya, Shigehiko Takegami, Atsushi Umemura and 1 more

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In one paragraph

Article in Frontiers in medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 89% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 2 institutions in 1 country.

Misaki MatsumotoDepartment of Pharmacology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Hikari SawadaDepartment of Pharmacology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Kazumi IwataDepartment of Pharmacology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Masakazu IbiDepartment of Pharmacology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Nozomi AsaokaDepartment of Pharmacology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Masato KatsuyamaRadioisotope Center, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Kaori Shintani-IshidaDepartment of Forensic Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Hiroshi IkegayaDepartment of Forensic Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Shigehiko TakegamiDepartment of Analytical Chemistry, Kyoto Pharmaceutical University, Kyoto, Japan.
Atsushi UmemuraDepartment of Pharmacology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Chihiro Yabe-NishimuraDepartment of Pharmacology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Kyoto Prefectural University of Medicine · JPKyoto Pharmaceutical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Various chemical probes for the detection of reactive oxygen species have been developed to examine oxidative stress associated with different pathologies. L-012, a luminol-based chemiluminescent probe, is widely used to detect extracellular superoxide because of its high sensitivity. We herein demonstrated that the co-application of the peptide boronic acid proteasome inhibitor, bortezomib, with L-012 significantly increased its luminescence without affecting the background. More than a 5-fold increase was detected in the total luminescence of L-012 in both NADPH oxidase-expressing cells and the xanthine oxidase-dependent cell-free superoxide generation system, but not in their background. Therefore, bortezomib increased the signal-to-background ratio and improved the detection of low levels of superoxide. The application of MLN2238, another peptide boronic acid proteasome inhibitor, also enhanced the luminescence of L-012. In contrast, carfilzomib, an epoxyketone proteasome inhibitor, did not increase luminescence, suggesting that the effects of bortezomib depend on the chemical structure of the peptide boronic acid, but not on its pharmacological effects. Bortezomib-induced enhancements appeared to be specific to the detection of superoxide because the detection of H

Indexed as

bortezomibNADPH oxidasepeptide boronic acidsuperoxidexanthine oxidase

Identifiers

PMID36619644
PMCPMC9811382
OpenAlexW4313466980

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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.