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pmid:36118521

Sex differences in hepatocellular carcinoma indicated BEX4 as a potential target to improve efficacy of lenvatinib plus immune checkpoint inhibitors.

Lu Liu · Kangkang Yu · Chong Huang · Meisi Huo · Xiaoqi Li · Ruiqi Yin · Chuanmiao Liu · Lu Lu · Huaping Sun · Jubo Zhang

Journal of Cancer · 2022 doi:10.7150/jca.73051

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

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Sex differences in hepatocellular carcinoma indicated BEX4 as a potential target to improve efficacy of lenvatinib plus immune checkpoint inhibitors.
doi
10.7150/jca.73051
pmid
36118521
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Lu Liu
[1]
Kangkang Yu
[2]
Chong Huang
[3]
Meisi Huo
[4]
Xiaoqi Li
[5]
Ruiqi Yin
[6]
Chuanmiao Liu
[7]
Lu Lu
[8]
Huaping Sun
[9]
Jubo Zhang
journal
Journal of Cancer
year
2022
abstract
Background: Hepatocellular carcinoma (HCC) is the most common form of liver cancer, and significant sex disparities have been observed in HCC. We aim to explore the potential sex-biased mechanisms involved in hepatocarcinogenesis. Methods: Based on TCGA data, we compared clinical features, genetic alterations, and immune cell infiltrations between male and female HCC patients. In addition, we performed sex-based differential expression analysis and functional enrichment analysis. Finally, GSE64041 dataset and another HCC cohort were engaged to validate our findings. Results: Significant differences of genetic alterations and TME were observed between male and female HCC patients. Enhanced metabolism of lipids was associated with hepatocarcinogenesis in men, while ECM-organization-related pathways were correlated to HCC development in women. BEX4 was upregulated in female but downregulated in male HCC patients, and was positively correlated with immune checkpoint molecules and infiltrated immune cell. These findings were further validated in dataset GSE64041 and our HCC cohort. More importantly, a negative correlation was found between BEX4 expression and lenvatinib sensitivity. Conclusion: Distinct biological processes were involved in sex-biased tumorigenesis of HCC. BEX4 can be targeted to improve the efficacy of lenvatinib plus immune checkpoint inhibitors.
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Gene expression profiling in paired human hepatocellular carcinoma and liver parenchyma biopsies and normal liver biopsies.
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36118521", "kind": "science-record", "revision": 5, "content_hash": "sha256:013689543f9c9f74df90948d1b65c302492f23a9f4710331ae153383e8f27eac", "created_at": "2026-11-01T18:15:23Z", "updated_at": "2026-11-01T22:50:07Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Sex differences in hepatocellular carcinoma indicated BEX4 as a potential target to improve efficacy of lenvatinib plus immune checkpoint inhibitors.", "doi": "10.7150/jca.73051", "pmid": "36118521", "authors": ["Lu Liu", "Kangkang Yu", "Chong Huang", "Meisi Huo", "Xiaoqi Li", "Ruiqi Yin", "Chuanmiao Liu", "Lu Lu", "Huaping Sun", "Jubo Zhang"], "journal": "Journal of Cancer", "year": 2022, "abstract": "Background: Hepatocellular carcinoma (HCC) is the most common form of liver cancer, and significant sex disparities have been observed in HCC. We aim to explore the potential sex-biased mechanisms involved in hepatocarcinogenesis. Methods: Based on TCGA data, we compared clinical features, genetic alterations, and immune cell infiltrations between male and female HCC patients. In addition, we performed sex-based differential expression analysis and functional enrichment analysis. Finally, GSE64041 dataset and another HCC cohort were engaged to validate our findings. Results: Significant differences of genetic alterations and TME were observed between male and female HCC patients. Enhanced metabolism of lipids was associated with hepatocarcinogenesis in men, while ECM-organization-related pathways were correlated to HCC development in women. BEX4 was upregulated in female but downregulated in male HCC patients, and was positively correlated with immune checkpoint molecules and infiltrated immune cell. These findings were further validated in dataset GSE64041 and our HCC cohort. More importantly, a negative correlation was found between BEX4 expression and lenvatinib sensitivity. Conclusion: Distinct biological processes were involved in sex-biased tumorigenesis of HCC. 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