A new finding in the key prognosis-related proto-oncogene FYN in hepatocellular carcinoma based on the WGCNA hub-gene screening trategy

Background: Hepatocellular carcinoma (HCC) is the third-most deadly cancer worldwide. More breakthroughs are needed in the clinical practice for liver cancer are needed, and new treatment strategies are required. This study aims to determine the significant differences in genes associated with LIHC...

Full description

Bibliographic Details
Main Authors: Guo, G. (Author), Huang, C. (Author), Nie, Y. (Author), Wang, A. (Author), Zhou, J. (Author), Zhu, X. (Author)
Format: Article
Language:English
Published: BioMed Central Ltd 2022
Subjects:
FYN
Online Access:View Fulltext in Publisher
LEADER 02921nam a2200553Ia 4500
001 10-1186-s12885-022-09388-5
008 220425s2022 CNT 000 0 und d
020 |a 14712407 (ISSN) 
245 1 0 |a A new finding in the key prognosis-related proto-oncogene FYN in hepatocellular carcinoma based on the WGCNA hub-gene screening trategy 
260 0 |b BioMed Central Ltd  |c 2022 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1186/s12885-022-09388-5 
520 3 |a Background: Hepatocellular carcinoma (HCC) is the third-most deadly cancer worldwide. More breakthroughs are needed in the clinical practice for liver cancer are needed, and new treatment strategies are required. This study aims to determine the significant differences in genes associated with LIHC and further analyze its prognostic value further. Methods: Here, we used the TCGA-LIHC database and the profiles of GSE25097 from GEO to explore the differentially co-expressed genes in HCC tissues compared with paratumor (or healthy) tissues. Then, we utilized WGCNA to screen differentially co-expressed genes. Finally, we explored the function of FYN in HCC cells and xenograft tumor models. Results: We identified ten hub genes in the protein–protein interaction (PPI) network, but only three (COLEC10, TGFBR3, and FYN) appeared closely related to the prognosis. The expression of FYN was positively correlated with the prognosis of HCC patients. The xenograft model showed that overexpression of FYN could significantly inhibit malignant tumor behaviors and promote tumor cell apoptosis. Conclusion: Thus, FYN may be central to the development of LIHC and maybe a novel biomarker for clinical diagnosis and treatment. © 2022, The Author(s). 
650 0 4 |a biology 
650 0 4 |a Biomarker 
650 0 4 |a Biomarkers, Tumor 
650 0 4 |a Carcinoma, Hepatocellular 
650 0 4 |a COLEC10 protein, human 
650 0 4 |a collectin 
650 0 4 |a Collectins 
650 0 4 |a Computational Biology 
650 0 4 |a FYN 
650 0 4 |a gene expression profiling 
650 0 4 |a Gene Expression Profiling 
650 0 4 |a gene expression regulation 
650 0 4 |a Gene Expression Regulation, Neoplastic 
650 0 4 |a gene regulatory network 
650 0 4 |a Gene Regulatory Networks 
650 0 4 |a genetics 
650 0 4 |a Hepatocellular carcinoma 
650 0 4 |a human 
650 0 4 |a Humans 
650 0 4 |a liver cell carcinoma 
650 0 4 |a Liver Neoplasms 
650 0 4 |a liver tumor 
650 0 4 |a metabolism 
650 0 4 |a pathology 
650 0 4 |a prognosis 
650 0 4 |a Prognosis 
650 0 4 |a proto oncogene 
650 0 4 |a Proto-Oncogenes 
650 0 4 |a tumor marker 
650 0 4 |a Weighted gene coexpressed network analysis 
700 1 |a Guo, G.  |e author 
700 1 |a Huang, C.  |e author 
700 1 |a Nie, Y.  |e author 
700 1 |a Wang, A.  |e author 
700 1 |a Zhou, J.  |e author 
700 1 |a Zhu, X.  |e author 
773 |t BMC Cancer