Evidence map›Paper›PMID 41898765›Full record

ArticleInternational journal of molecular sciences2026

Exploring the Role of GGA2 in Cancer Progression: Pan-Cancer Bioinformatics and Experimental Validation in Prostate Cancer.

Yangyang Han, Ziyu Huang, Yuxuan Zou, Yunbo Zhang, Huizhen Xin, Meng Sun, Yimin Liu, Mengqi Zhang, Mengjia Li

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. 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
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

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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.

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

9 authors.

Yangyang HanDepartment of Biology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi 830017, China.ORCID 0009-0005-9284-5530
Ziyu HuangDepartment of Biology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi 830017, China.
Yuxuan ZouDepartment of Biology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi 830017, China.
Yunbo ZhangDepartment of Biology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi 830017, China.
Huizhen XinDepartment of Biology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi 830017, China.
Meng SunDepartment of Biology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi 830017, China.
Yimin LiuDepartment of Biology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi 830017, China.
Mengqi ZhangDepartment of Biology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi 830017, China.
Mengjia LiDepartment of Biology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi 830017, China.ORCID 0000-0002-2767-9266

Funding

the National Natural Science Foundation of China 32300465the National Natural Science Foundation of China 81902580Xinjiang Key Laboratory of Molecular Biology for Endemic Diseases XJDFB2024G02
6 · The paper itself

Abstract

Cancer remains a significant challenge to global public health. Preliminary studies indicate that the protein Golgi-associated, Gamma-adaptin Ear Containing, ARF Binding Protein 2 (GGA2) may influence various cancers. However, the potential role of GGA2 in oncogenesis remains unknown. We utilized data from The Cancer Genome Atlas (TCGA) and the Genotype-Tissue Expression (GTEx) projects to analyze GGA2 expression levels. Genetic variations and protein expression of GGA2 in human tissues were assessed using the cBioPortal. Gene Set Enrichment Analysis (GSEA) provided deeper insights into GGA2's oncogenic functions. Comprehensive analysis of TCGA datasets combined with ESTIMATE and TIMER tools demonstrated significant correlations between GGA2 expression levels and clinical outcomes, survival metrics, genomic instability markers (microsatellite instability (MSI)/tumor mutational burden (TMB)), and immune microenvironment composition. Functional validation in prostate cancer models employed qRT-PCR quantification, immunoblotting verification, and cellular behavior assessments through colony formation, Transwell migration, and wound closure assays. Our findings suggest GGA2 could serve as a prognostic biomarker in various cancers. Abnormal levels of GGA2 promoter methylation and genetic alterations may contribute to its dysregulated expression in some cancers. Distinctly, GGA2 expression correlates with MSI and TMB across different cancers and is linked to the expression of immune checkpoint genes. Functionally, GGA2 is instrumental in inhibiting oncogenic mechanisms by diminishing the proliferation, colony formation, invasion, and migratory capabilities of prostate cancer cells. Our study shows that the oncogenic role of GGA2 in various cancers and GGA2 could be served as a biomarker of PARD.

Indexed as

Adaptor Proteins, Vesicular TransportComputational BiologyProstatic NeoplasmsBiomarkers, TumorCell Line, TumorDisease ProgressionDNA MethylationGene Expression Regulation, NeoplasticHumansMaleMicrosatellite InstabilityPrognosisPromoter Regions, GeneticAdaptor Proteins, Vesicular TransportBiomarkers, TumorGGA2immunepan-cancerprognostic biomarkerprostate cancer

Identifiers

PMID41898765
PMCPMC13026977

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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.