GPC-3 and AXL are essential factors and therapeutic targets for hepatocellular carcinoma

Abstract Purpose The aim of this study was to determine the expression of Glypican-3(GPC-3) and AXL in hepatocellular carcinomas (HCCs). Methods A total of 140 patients diagnosed with HCC were included in this study. All patients had undergone radical surgery and had complete clinical information. Formalin-fixed paraffin-embedded tissue blocks of HCC from these patients were collected, and the expression levels of GPC-3 and AXL were detected by immunohistochemical (IHC) staining. Results Immunohistochemical analysis showed that GPC-3 and AXL were diffusely expressed in HCCs. The positive expression rate of GPC-3 was 77.1% (108/140) and that of AXL was 85.7% (120/140). Additionally, the proportion of cases with positive expression for either GPC-3 or AXL is 93.6%. Conclusions The findings of this study confirm that both GPC-3 and AXL are highly expressed in HCCs tissues, and the high co-expression rate supports the development of dual-target chimeric antigen receptor T (CAR-T) cell therapy for HCC treatment.

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Publication Details

Journal
Clinical Cancer Bulletin
Published
2025-10-27
DOI
https://doi.org/10.1007/s44272-025-00051-1
Citations
1
Primary Topic
Phagocytosis and Immune Regulation
Type
article
Field-Weighted Citation Impact
0.80

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article

GPC-3 and AXL are essential factors and therapeutic targets for hepatocellular carcinoma

Cuisong Zhu, Jianqing Xu, Yan Su, Xiaowu Huang et al.
1 citations
Clinical Cancer Bulletin
Phagocytosis and Immune Regulation
0.80
article

GPC-3 and AXL are essential factors and therapeutic targets for hepatocellular carcinoma

Cuisong Zhu, Jianqing Xu, Yan Su, Xiaowu Huang, Chao Qiu, Xiaoyan Zhang, Shuye Zhang, Jie-Yi Shi, Yanling Feng
article en
1 citations

Abstract

Abstract Purpose The aim of this study was to determine the expression of Glypican-3(GPC-3) and AXL in hepatocellular carcinomas (HCCs). Methods A total of 140 patients diagnosed with HCC were included in this study. All patients had undergone radical surgery and had complete clinical information. Formalin-fixed paraffin-embedded tissue blocks of HCC from these patients were collected, and the expression levels of GPC-3 and AXL were detected by immunohistochemical (IHC) staining. Results Immunohistochemical analysis showed that GPC-3 and AXL were diffusely expressed in HCCs. The positive expression rate of GPC-3 was 77.1% (108/140) and that of AXL was 85.7% (120/140). Additionally, the proportion of cases with positive expression for either GPC-3 or AXL is 93.6%. Conclusions The findings of this study confirm that both GPC-3 and AXL are highly expressed in HCCs tissues, and the high co-expression rate supports the development of dual-target chimeric antigen receptor T (CAR-T) cell therapy for HCC treatment.

Clinical Cancer BulletinVol. 4(1)
Xiamen University (CN), Fudan University (CN), Shanghai Public Health Clinical Center (CN), Zhongshan Hospital of Xiamen University (CN), Zhongshan Hospital (CN), YangPu Geriatric Hospital (CN), Xiamen University of Technology (CN)
Science and Technology Commission of Shanghai Municipality
Openalex Percentile: Top 22%
Phagocytosis and Immune Regulation
0.80
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