Proteomics Identifies LUC7L3 as a Prognostic Biomarker for Hepatocellular Carcinoma

Bibliographic Details
Title: Proteomics Identifies LUC7L3 as a Prognostic Biomarker for Hepatocellular Carcinoma
Authors: Yushan Hou, Siqi Wang, Yiming Zhang, Xiaofen Huang, Xiuyuan Zhang, Fuchu He, Chunyan Tian, Aihua Sun
Source: Current Issues in Molecular Biology, Vol 46, Iss 5, Pp 4004-4020 (2024)
Publisher Information: MDPI AG, 2024.
Publication Year: 2024
Collection: LCC:Biology (General)
Subject Terms: hepatocellular carcinoma, alternative splicing, LUC7L3, RRM2, prognostic biomarker, Biology (General), QH301-705.5
More Details: Alternative splicing has been shown to participate in tumor progression, including hepatocellular carcinoma. The poor prognosis of patients with HCC calls for molecular classification and biomarker identification to facilitate precision medicine. We performed ssGSEA analysis to quantify the pathway activity of RNA splicing in three HCC cohorts. Kaplan–Meier and Cox methods were used for survival analysis. GO and GSEA were performed to analyze pathway enrichment. We confirmed that RNA splicing is significantly correlated with prognosis, and identified an alternative splicing-associated protein LUC7L3 as a potential HCC prognostic biomarker. Further bioinformatics analysis revealed that high LUC7L3 expression indicated a more progressive HCC subtype and worse clinical features. Cell proliferation-related pathways were enriched in HCC patients with high LUC7L3 expression. Consistently, we proved that LUC7L3 knockdown could significantly inhibit cell proliferation and suppress the activation of associated signaling pathways in vitro. In this research, the relevance between RNA splicing and HCC patient prognosis was outlined. Our newly identified biomarker LUC7L3 could provide stratification for patient survival and recurrence risk, facilitating early medical intervention before recurrence or disease progression.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1467-3045
1467-3037
Relation: https://www.mdpi.com/1467-3045/46/5/247; https://doaj.org/toc/1467-3037; https://doaj.org/toc/1467-3045
DOI: 10.3390/cimb46050247
Access URL: https://doaj.org/article/ebfd8a674e9f468480b9e7f0d5982f64
Accession Number: edsdoj.bfd8a674e9f468480b9e7f0d5982f64
Database: Directory of Open Access Journals
More Details
ISSN:14673045
14673037
DOI:10.3390/cimb46050247
Published in:Current Issues in Molecular Biology
Language:English