Evidence map›Paper›PMID 40890493›Full record

ArticleDiscover oncology2025

Integrated pan-cancer and melanoma-specific analysis of angiopoietin-2: prognostic value, immune microenvironment modulation, and ceRNA network regulation.

Xuejun Ni, Xiaofen Wan, Beichen Cai, Hongteng Xie, Lu Chen, Qian Lin, Ruonan Ke, Tao Huang, Heyan Ye, Xiuying Shan and 1 more

Abstract read
In one paragraph

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 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. Article
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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

11 authors.

Xuejun Ni *Department of Plastic Surgery, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, China.
Xiaofen Wan *Department of Plastic Surgery, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, China.
Beichen Cai *Department of Plastic Surgery, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, China.
Hongteng XieBurn & Wound Repair Department, Fujian Medical University Union Hospital, Fuzhou, 350001, China.
Lu ChenDepartment of Plastic Surgery, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, China.
Qian LinDepartment of Plastic Surgery, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, China.
Ruonan KeDepartment of Plastic Surgery, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, China.
Tao HuangDepartment of Plastic Surgery, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, China.
Heyan YeDepartment of Plastic Surgery, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, China.
Xiuying ShanDepartment of Plastic Surgery, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, China. xiuyingshan@fjmu.edu.cn.
Biao WangDepartment of Plastic Surgery, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, China. biaowang@fjmu.edu.cn.

Funding

National Natural Science Foundation of China No.82472576Natural Science Fundation of Fujian Province No.2021J01244Natural Science Fundation of Fujian Province No. 2024J08167
6 · The paper itself

Abstract

objectiveThis research seeks to comprehensively explore the expression patterns of Angiopoietin-2 (ANGPT2) in pan-cancer and examine its relationship with clinical outcomes, tumor immune microenvironment dynamics, and biological functions, with particular emphasis on skin cutaneous melanoma (SKCM).

methodsData from six databases, including UCSC Xena, TCGA, GTEx, TIMER2.0, GEPIA, and cBioPortal, were analyzed to assess ANGPT2 expression in pan-cancer. Immunohistochemical images were sourced from the HPA database. We explored the correlation between ANGPT2 expression and prognosis, diagnostic value, genetic alterations, and immune cell infiltration in cancers. Functional enrichment and gene set enrichment analyses were performed to uncover the biological roles of ANGPT2. Additionally, miRWalk, miRDB, Starbase 2.0 ENCORI, and Cytoscape were utilized to identify and construct the lncRNA-miRNA-ANGPT2 ceRNA regulatory network in SKCM.

resultsOur comprehensive pan-cancer analysis revealed that ANGPT2 undergoes genetic alterations in several tumor types, including mutations, amplifications, and deep deletions. ANGPT2 expression varies across cancers, with high levels detected in 21 tumor types. ANGPT2 demonstrated significant diagnostic and prognostic value in various cancers. Genes related to ANGPT2 in cancers with high expression were found to be involved in critical pathways such as tumor angiogenesis, growth factor signaling, extracellular matrix (ECM) structure, and cell surface receptor activation. In addition, ANGPT2 was found to modulate the immune microenvironment in multiple tumors, promoting immune evasion and contributing to tumor progression, particularly in SKCM. A lncRNA-miRNA-ANGPT2 ceRNA regulatory network was identified, which may play a role in SKCM progression.

conclusionsANGPT2 demonstrates potential as a biomarker for cancer diagnosis and prognosis, with evidence suggesting its involvement in immune microenvironment regulation and associated gene networks. Therapeutic approaches targeting ANGPT2, either as a stand-alone treatment or in combination with immunotherapies, could offer new and effective strategies for future cancer treatments.

Indexed as

Angiopoietin-2ceRNA networkImmune microenvironmentIntegrative analysisMelanomaPan-cancer

Identifiers

PMID40890493
PMCPMC12401860

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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.