Characterization of lactylation modification subtypes and the promoting role of CCL20 in hepatocellular carcinoma progression
- Li-Hong Wu 1, Liu Yang 1, Xiang-Xu Wang 2, Shuang Bai 3, Xi Yan 1, Jing Wei 1, Jun Wang 1, Fei Tian 2
- Li-Hong Wu 1, Liu Yang 1, Xiang-Xu Wang 2
- 1Department of Gastroenterology, Xijing 986 Hospital, Fourth Military Medical University, Xi'an, China.
- 2Department of Clinical Oncology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
- 3Department of Oncology, Xi'an People's Hospital (Xi'an Fourth Hospital), Xi'an, China.
- 0Department of Gastroenterology, Xijing 986 Hospital, Fourth Military Medical University, Xi'an, China.
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View abstract on PubMed
Summary
This summary is machine-generated.This study identifies a six-gene lactylation modification-based prognostic model (LRPS) for hepatocellular carcinoma (HCC). Higher LRPS scores indicate worse prognosis and correlate with immune cell infiltration, highlighting CCL20 as a key driver gene.
Area Of Science
- Oncology
- Biochemistry
- Molecular Biology
Background
- Hepatocellular carcinoma (HCC) is an aggressive malignancy with a need for improved prognostic factors.
- Lactylation modification is implicated in tumorigenesis, but its role and related genes in HCC are not fully understood.
Purpose Of The Study
- To identify prognostically significant lactylation modification-related genes in HCC.
- To develop and validate a lactylation modification-based prognostic model for HCC patients.
- To investigate the role of lactylation in the tumor immune microenvironment and HCC progression.
Main Methods
- Screening of lactylation-related genes using expression data and patient survival outcomes (DFS, PFS, OS).
- Stratification of HCC patients into subtypes using Non-negative Matrix Factorization (NMF).
- Construction and validation of a prognostic model using LASSO-Cox and multivariate Cox regression; analysis of immune cell infiltration via CIBERSORT; in vitro validation of CCL20.
Main Results
- Three lactylation modification patterns were identified, with higher levels associated with poorer HCC prognosis.
- A six-gene prognostic model (LRPS: FAM83D, ENO1, PFN2, LCAT, PTGR1, CCL20) was developed and validated, showing reduced survival in high-risk groups.
- The LRPS correlated with TP53 mutations, immune cell infiltration (M0 macrophages, Tregs, neutrophils), and CCL20 overexpression enhanced HCC cell proliferation and migration.
Conclusions
- A novel lactylation modification-based prognostic model (LRPS) accurately predicts HCC patient outcomes.
- The LRPS is linked to glucose metabolism and immune infiltration patterns.
- CCL20 is a key gene in the model, promoting HCC progression and serving as a potential prognostic biomarker and therapeutic target.
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