RASGRF2 as a potential pathogenic gene mediating the progression of alcoholic hepatitis to alcohol-related cirrhosis and hepatocellular carcinoma
Abstract Background and aims Alcoholic hepatitis (AH) and hepatocellular carcinoma (HCC) are common liver diseases. Chronic inflammation caused by AH can progress to alcoholic cirrhosis (AC) and eventually HCC. Methods This study sought to ascertain potential shared genes between AH and HCC through...
Saved in:
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Springer
2025-01-01
|
Series: | Discover Oncology |
Subjects: | |
Online Access: | https://doi.org/10.1007/s12672-025-01853-4 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1832571512736972800 |
---|---|
author | Zhengyuan Chen Danfeng Fan Tianyi Hang Xiaoqing Yue |
author_facet | Zhengyuan Chen Danfeng Fan Tianyi Hang Xiaoqing Yue |
author_sort | Zhengyuan Chen |
collection | DOAJ |
description | Abstract Background and aims Alcoholic hepatitis (AH) and hepatocellular carcinoma (HCC) are common liver diseases. Chronic inflammation caused by AH can progress to alcoholic cirrhosis (AC) and eventually HCC. Methods This study sought to ascertain potential shared genes between AH and HCC through the utilization of multiple transcriptome databases. Employing an immune infiltration analysis, and calculating the correlation between shared genes and immune infiltration results, in conjunction with independent bulk transcriptome validation sets, led to the identification of core shared genes. Subsequently, single-cell transcriptome data, clinical sample immunohistochemistry experiments, and overexpressed core shared genes in HepG2 cells were employed to validate the core shared genes of AH and HCC. Results Through the bulk transcriptome discovery sets of AH and HCC, 206 potential shared genes were identified. After screening with two machine learning algorithms, five shared genes remained. Combining the results of the immune infiltration and bulk transcriptome results from an independent validation cohort, the core shared gene was determined to be RASGRF2. Single-cell data further demonstrated that RASGRF2 and its downstream genes were highly expressed in AH, AC, and HCC tissues. Spatial transcriptome data indicated that RASGRF2 was highly expressed in HCC tumor tissues. Compared with the paracancerous tissues, the RASGRF2 gene was significantly overexpressed in HCC tissues. Overexpression of RASGRF2 in HepG2 cells resulted in significantly enhanced migration, invasion, and proliferation abilities. Conclusion RASGRF2 serve as a pathogenic gene that mediates the progression of AH to AC and potentially to HCC. |
format | Article |
id | doaj-art-521690c317ba419e8462c363c0073813 |
institution | Kabale University |
issn | 2730-6011 |
language | English |
publishDate | 2025-01-01 |
publisher | Springer |
record_format | Article |
series | Discover Oncology |
spelling | doaj-art-521690c317ba419e8462c363c00738132025-02-02T12:30:41ZengSpringerDiscover Oncology2730-60112025-01-0116111710.1007/s12672-025-01853-4RASGRF2 as a potential pathogenic gene mediating the progression of alcoholic hepatitis to alcohol-related cirrhosis and hepatocellular carcinomaZhengyuan Chen0Danfeng Fan1Tianyi Hang2Xiaoqing Yue3Nanjing University of Chinese MedicineNanjing University of Chinese MedicineNanjing University of Chinese MedicineNanjing University of Chinese MedicineAbstract Background and aims Alcoholic hepatitis (AH) and hepatocellular carcinoma (HCC) are common liver diseases. Chronic inflammation caused by AH can progress to alcoholic cirrhosis (AC) and eventually HCC. Methods This study sought to ascertain potential shared genes between AH and HCC through the utilization of multiple transcriptome databases. Employing an immune infiltration analysis, and calculating the correlation between shared genes and immune infiltration results, in conjunction with independent bulk transcriptome validation sets, led to the identification of core shared genes. Subsequently, single-cell transcriptome data, clinical sample immunohistochemistry experiments, and overexpressed core shared genes in HepG2 cells were employed to validate the core shared genes of AH and HCC. Results Through the bulk transcriptome discovery sets of AH and HCC, 206 potential shared genes were identified. After screening with two machine learning algorithms, five shared genes remained. Combining the results of the immune infiltration and bulk transcriptome results from an independent validation cohort, the core shared gene was determined to be RASGRF2. Single-cell data further demonstrated that RASGRF2 and its downstream genes were highly expressed in AH, AC, and HCC tissues. Spatial transcriptome data indicated that RASGRF2 was highly expressed in HCC tumor tissues. Compared with the paracancerous tissues, the RASGRF2 gene was significantly overexpressed in HCC tissues. Overexpression of RASGRF2 in HepG2 cells resulted in significantly enhanced migration, invasion, and proliferation abilities. Conclusion RASGRF2 serve as a pathogenic gene that mediates the progression of AH to AC and potentially to HCC.https://doi.org/10.1007/s12672-025-01853-4Alcoholic hepatitisHepatocellular carcinomaBulk transcriptomeSingle-cell transcriptomeSpatial transcriptomeHepG2 |
spellingShingle | Zhengyuan Chen Danfeng Fan Tianyi Hang Xiaoqing Yue RASGRF2 as a potential pathogenic gene mediating the progression of alcoholic hepatitis to alcohol-related cirrhosis and hepatocellular carcinoma Discover Oncology Alcoholic hepatitis Hepatocellular carcinoma Bulk transcriptome Single-cell transcriptome Spatial transcriptome HepG2 |
title | RASGRF2 as a potential pathogenic gene mediating the progression of alcoholic hepatitis to alcohol-related cirrhosis and hepatocellular carcinoma |
title_full | RASGRF2 as a potential pathogenic gene mediating the progression of alcoholic hepatitis to alcohol-related cirrhosis and hepatocellular carcinoma |
title_fullStr | RASGRF2 as a potential pathogenic gene mediating the progression of alcoholic hepatitis to alcohol-related cirrhosis and hepatocellular carcinoma |
title_full_unstemmed | RASGRF2 as a potential pathogenic gene mediating the progression of alcoholic hepatitis to alcohol-related cirrhosis and hepatocellular carcinoma |
title_short | RASGRF2 as a potential pathogenic gene mediating the progression of alcoholic hepatitis to alcohol-related cirrhosis and hepatocellular carcinoma |
title_sort | rasgrf2 as a potential pathogenic gene mediating the progression of alcoholic hepatitis to alcohol related cirrhosis and hepatocellular carcinoma |
topic | Alcoholic hepatitis Hepatocellular carcinoma Bulk transcriptome Single-cell transcriptome Spatial transcriptome HepG2 |
url | https://doi.org/10.1007/s12672-025-01853-4 |
work_keys_str_mv | AT zhengyuanchen rasgrf2asapotentialpathogenicgenemediatingtheprogressionofalcoholichepatitistoalcoholrelatedcirrhosisandhepatocellularcarcinoma AT danfengfan rasgrf2asapotentialpathogenicgenemediatingtheprogressionofalcoholichepatitistoalcoholrelatedcirrhosisandhepatocellularcarcinoma AT tianyihang rasgrf2asapotentialpathogenicgenemediatingtheprogressionofalcoholichepatitistoalcoholrelatedcirrhosisandhepatocellularcarcinoma AT xiaoqingyue rasgrf2asapotentialpathogenicgenemediatingtheprogressionofalcoholichepatitistoalcoholrelatedcirrhosisandhepatocellularcarcinoma |