Evidence map›Paper›PMID 41577808›Full record

ArticleScientific reports2026

Functional characterization of angiogenesis genes in hepatocellular carcinoma via integrated bulk and single cell RNA sequencing.

Jiayi Zhang, Wei Liu, Xiaorui Liu, Xu Wang, Kai Tang, Chengtao Sun, Tielong Wang, Shuqiang Liu, Xiaoshun He

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Jiayi Zhang *Organ Transplant Center, The First Affiliated Hospital, Sun Yat-sen University, NO.58 Zhongshan Er Road, Guangzhou, 510080, China.
Wei Liu *State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, 510060, China.
Xiaorui Liu *Organ Transplant Center, The First Affiliated Hospital, Sun Yat-sen University, NO.58 Zhongshan Er Road, Guangzhou, 510080, China.
Xu Wang *Tianjin Huaxing Hospital, Tianjin, China.
Kai TangSchool of Pharmaceutical Sciences, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, 250117, China. tangkai1995@sdfmu.edu.cn.
Chengtao SunDepartment of Oncology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Lung Cancer Institute, Jinan, Shandong Province, China. mysuna@126.com.
Tielong WangOrgan Transplant Center, The First Affiliated Hospital, Sun Yat-sen University, NO.58 Zhongshan Er Road, Guangzhou, 510080, China. wangtlong5@mail2.sysu.edu.cn.
Shuqiang LiuSchool of Pharmaceutical Sciences, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, 250117, China. lshq120@163.com.
Xiaoshun HeOrgan Transplant Center, The First Affiliated Hospital, Sun Yat-sen University, NO.58 Zhongshan Er Road, Guangzhou, 510080, China. gdtrc@163.com.

Funding

National Natural Science Foundation of China 82070670Shandong Postdoctoral Science Foundation SDCX-ZG-202301013Shandong Provincial Natural Science Foundation ZR2022MH245
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) originates from hepatocytes and accounts for over 80% of primary liver cancers. Despite numerous studies have explained the role of certain angiogenesis-related and integrated stress response related genes in the development of HCC, few studies have explored the function of all angiogenesis-related and ISR(Integrated stress response)-related genes, as well as their applications in therapeutic prediction models. Here, by integrating bulk and single cell transcriptome data, We first explored the expression patterns of genes at the intersection of angiogenesis and the integrated stress response (ISR). To comprehensively identify angiogenesis-related gene modules, we then performed WGCNA (weighted gene co-expression network analysis) using a broader angiogenesis gene set, revealing modules strongly correlated with angiogenic activity.Based on these core genes, we constructed a prognostic model to evaluate patient outcomes and responses to immunotherapy, which is valuable for informing treatment options. Furthermore, through drug response modeling, we identified several drugs targeting angiogenesis genes that could serve as potential therapeutic options. Single-cell transcriptome analysis also revealed that DAB2, which is highly expressed in APOA2+ macrophages, may be involved in the cellular response to signals from fibroblast cells via the THY1 pathway. Finally, molecular docking studies indicated that dihydroergotamine might be a promising candidate drug for targeting DAB2. This study systematically investigated the expression changes of angiogenesis genes in HCC, constructed a tumor prognosis prediction model, and explored potential therapeutic targets and drugs. These findings are of significance for guiding the selection of treatment options and identifying therapeutic targets for HCC.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsNeovascularization, PathologicGene Expression ProfilingGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansPrognosisSequence Analysis, RNASingle-Cell AnalysisSingle-Cell Gene Expression AnalysisTranscriptomeAngiogenesisDAB2HCCMulti-omicsPrognosis model

Identifiers

PMID41577808
PMCPMC12830787

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LicenceCC BY-NC-ND
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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.