Evidence map›Paper›PMID 36172978›Full record

ReviewMolecules and cells2022

Glyoxalase 1 as a Therapeutic Target in Cancer and Cancer Stem Cells.

Ji-Young Kim, Ji-Hye Jung, Seung-Joon Lee, Seon-Sook Han, Seok-Ho Hong

Open access · diamondAbstract readReview
In one paragraph

Review in Molecules and cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 30 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

5 authors at 1 institution in 1 country.

Ji-Young KimDepartment of Internal Medicine, School of Medicine, Kangwon National University, Chuncheon 24341, Korea.ORCID https://orcid.org/0000-0002-0112-2603
Ji-Hye JungDepartment of Internal Medicine, School of Medicine, Kangwon National University, Chuncheon 24341, Korea.ORCID https://orcid.org/0000-0003-1638-8823
Seung-Joon LeeDepartment of Internal Medicine, School of Medicine, Kangwon National University, Chuncheon 24341, Korea.ORCID https://orcid.org/0000-0003-4597-0281
Seon-Sook HanDepartment of Internal Medicine, School of Medicine, Kangwon National University, Chuncheon 24341, Korea.ORCID https://orcid.org/0000-0002-1320-4163
Seok-Ho HongDepartment of Internal Medicine, School of Medicine, Kangwon National University, Chuncheon 24341, Korea.ORCID https://orcid.org/0000-0003-3372-442X
Kangwon National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Methylglyoxal (MG) is a dicarbonyl compound formed in cells mainly by the spontaneous degradation of the triose phosphate intermediates of glycolysis. MG is a powerful precursor of advanced glycation end products, which lead to strong dicarbonyl and oxidative stress. Although divergent functions of MG have been observed depending on its concentration, MG is considered to be a potential anti-tumor factor due to its cytotoxic effects within the oncologic domain. MG detoxification is carried out by the glyoxalase system. Glyoxalase 1 (Glo1), the ubiquitous glutathione-dependent enzyme responsible for MG degradation, is considered to be a tumor promoting factor due to it catalyzing the removal of cytotoxic MG. Indeed, various cancer types exhibit increased expression and activity of Glo1 that closely correlate with tumor cell growth and metastasis. Furthermore, mounting evidence suggests that Glo1 contributes to cancer stem cell survival. In this review, we discuss the role of Glo1 in the malignant progression of cancer and its possible use as a promising therapeutic target for tumor therapy. We also summarize therapeutic outcomes of Glo1 inhibitors as prospective treatments for the prevention of cancer.

Indexed as

Antineoplastic AgentsLactoylglutathione LyaseNeoplasmsHumansOxidative StressAntineoplastic AgentsLactoylglutathione Lyasecancercancer stem cellglyoxalase 1methylglyoxal

Identifiers

PMID36172978
PMCPMC9794553
OpenAlexW4297965553

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.