Evidence map›Paper›PMID 38870176›Full record

ArticlePloS one2024

Glyoxalase 1: Emerging biomarker and therapeutic target in cervical cancer progression.

Ji-Young Kim, Ji-Hye Jung, Soryung Jung, Sanghyuk Lee, Hyang Ah Lee, Yung-Taek Ouh, Seok-Ho Hong

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. 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

7 authors.

Ji-Young KimDepartment of Internal Medicine, School of Medicine, Kangwon National University, Chuncheon, Republic of Korea.
Ji-Hye JungDepartment of Internal Medicine, School of Medicine, Kangwon National University, Chuncheon, Republic of Korea.
Soryung JungDepartment of Life Science, Ewha Womans University, Seoul, Republic of Korea.ORCID 0009-0003-0501-4399
Sanghyuk LeeDepartment of Life Science, Ewha Womans University, Seoul, Republic of Korea.
Hyang Ah LeeDepartment of Obstetrics and Gynecology, School of Medicine, Kangwon National University, Chuncheon, Republic of Korea.
Yung-Taek OuhDepartment of Obstetrics and Gynecology, School of Medicine, Kangwon National University, Chuncheon, Republic of Korea.ORCID 0000-0001-5887-4497
Seok-Ho HongDepartment of Internal Medicine, School of Medicine, Kangwon National University, Chuncheon, Republic of Korea.ORCID 0000-0003-3372-442X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCervical cancer presents a significant global health challenge, disproportionately impacting underserved populations with limited access to healthcare. Early detection and effective management are vital in addressing this public health concern. This study focuses on Glyoxalase-1 (GLO1), an enzyme crucial for methylglyoxal detoxification, in the context of cervical cancer.

methodsWe assessed GLO1 expression in cervical cancer patient samples using immunohistochemistry. In vitro experiments using HeLa cells were conducted to evaluate the impact of GLO1 inhibition on cell viability and migration. Single-cell RNA sequencing (scRNA-seq) and gene set variation analysis were utilized to investigate the role of GLO1 in the metabolism of cervical cancer. Additionally, public microarray data were analyzed to determine GLO1 expression across various stages of cervical cancer.

resultsOur analysis included 58 cervical cancer patients, and showed that GLO1 is significantly upregulated in cervical cancer tissues compared to normal cervical tissues, independent of pathological findings and disease stage. In vitro experiments indicated that GLO1 inhibition by S-p-bromobenzylglutathione cyclopentyl diester decreased cell viability and migration in cervical cancer cell lines. Analyses of scRNA-seq data and public gene expression datasets corroborated the overexpression of GLO1 and its involvement in cancer metabolism, particularly glycolysis. An examination of expression data from precancerous lesions revealed a progressive increase in GLO1 expression from normal tissue to invasive cervical cancer.

conclusionsThis study highlights the critical role of GLO1 in the progression of cervical cancer, presenting it as a potential biomarker and therapeutic target. These findings contribute valuable insights towards personalized treatment approaches and augment the ongoing efforts to combat cervical cancer. Further research is necessary to comprehensively explore GLO1's potential in clinical applications.

Indexed as

Biomarkers, TumorLactoylglutathione LyaseUterine Cervical NeoplasmsAdultCell Line, TumorCell MovementCell SurvivalDisease ProgressionFemaleGene Expression Regulation, NeoplasticHeLa CellsHumansMiddle AgedBiomarkers, TumorGLO1 protein, humanLactoylglutathione Lyase

Identifiers

PMID38870176
PMCPMC11175447

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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.