ArticleDiscover oncology2025
PGLS as an immune and prognostic biomarker: from pan-cancer analysis to validation.
Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Glucose metabolism in tumor-associated macrophage plasticity and cancer immunity.Frontiers in cell and developmental biology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
6-phosphogluconolactonase (PGLS) is a metabolic enzyme of the pentose phosphate pathway that has been linked to tumorigenesis in several cancers. However, its role in pan-cancer remains unclear. This study reveals the expression profile and prognostic analysis of PGLS in different cancers by pan-cancer analysis. We utilized mRNA-seq data from TCGA and GTEx databases to analyze PGLS expression in different tumors. PGLS expression was significantly higher in almost all types of human cancer tissues compared to corresponding normal tissues. High PGLS expression was linked to poor prognosis. PGLS expression was significantly associated with immune regulatory genes, immune cell infiltration, tumor heterogeneity, tumor stemness, and involved in the regulation of anticancer drug sensitivity. Knockdown of PGLS resulted in slowed growth and diminished migratory and invasive capacity of Huh7 and A498 cells. Additionally, PGLS knockdown led to an increase in M1 macrophages, CD8
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.