Single-cell and spatial analyses of the GDF family in tumors, with a focus on the prognostic and biological role of GDF15 in hepatocellular carcinoma

Growth differentiation factors (GDFs) are a subfamily of the TGF-β superfamily whose expression increases in response to cellular stress and disease. Despite emerging cell- or animal-based evidence supporting an association between the GDF subfamily and cancer, systematic pan-cancer analyses of the GDF subfamily based on single-cell and spatial transcriptomes remains unavailable. In this study, we performed a comprehensive analysis of the GDF subfamily in 33 cancers, including expression, diagnosis, methylation, prognostic value, immune infiltration analysis, and potential biological pathways. We focused on the analysis of multi-group scRNA-seq and spatial data in hepatocellular carcinoma (HCC) to determine the role of the GDF family in the tumor microenvironment and its applicability in immunotherapy. Moreover, both the gain and loss of function strategies were used to assess the function of Growth differentiation factor 15 (GDF15) in cell lines of HCC. The GDF subfamily is expressed to varying degrees in most tumors and is significantly correlated with the prognosis of cancer patients. Subsequent scRNA-seq analysis depicted the heterogeneous cellular ecosystems of normal liver and HCC. Hepatocytes expressing GDF15 were less differentiated in HCC, and GDF15 promoted proliferation and invasion of HCC cell lines. Compared to normal liver, the strength of crosstalk between GDF15-positive Hepatocytes and other cells was enhanced in tumors, especially cancer-associated fibroblasts (CAFs)-derived Periostin and GDF15-positive Hepatocytes both regulate each other and jointly promote hepatocarcinogenesis. Further spatial transcriptomic data showed that GDF15 expression was negatively correlated with immune infiltration, especially in M1-type macrophages. Notably, validation analyses in bulk RNA-seq consistently emphasized the clinical significance of these findings. This study provides a comprehensive overview of the oncogenic role of the GDF subfamily in a wide range of tumors, highlights the important role of GDF15 in HCC ecosystem, and provides important biomarkers and potential therapeutic targets for future research.

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Journal
Cell & Bioscience
Published
2025-06-27
DOI
https://doi.org/10.1186/s13578-025-01431-9
Primary Topic
GDF15 and Related Biomarkers
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article
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article

Single-cell and spatial analyses of the GDF family in tumors, with a focus on the prognostic and biological role of GDF15 in hepatocellular carcinoma

Xiaoqian Feng, Wenkang Yuan, Y. Zhu, Fu‐Min Zhang et al.
Cell & Bioscience
GDF15 and Related Biomarkers
article

Single-cell and spatial analyses of the GDF family in tumors, with a focus on the prognostic and biological role of GDF15 in hepatocellular carcinoma

Xiaoqian Feng, Wenkang Yuan, Y. Zhu, Fu‐Min Zhang, Qian Huai, Bo Tao, Ying Dai, Xingyu Li, Haoran Zhang, Xu Zhang, Zhuo Yu, Yishan Du
article en

Abstract

Growth differentiation factors (GDFs) are a subfamily of the TGF-β superfamily whose expression increases in response to cellular stress and disease. Despite emerging cell- or animal-based evidence supporting an association between the GDF subfamily and cancer, systematic pan-cancer analyses of the GDF subfamily based on single-cell and spatial transcriptomes remains unavailable. In this study, we performed a comprehensive analysis of the GDF subfamily in 33 cancers, including expression, diagnosis, methylation, prognostic value, immune infiltration analysis, and potential biological pathways. We focused on the analysis of multi-group scRNA-seq and spatial data in hepatocellular carcinoma (HCC) to determine the role of the GDF family in the tumor microenvironment and its applicability in immunotherapy. Moreover, both the gain and loss of function strategies were used to assess the function of Growth differentiation factor 15 (GDF15) in cell lines of HCC. The GDF subfamily is expressed to varying degrees in most tumors and is significantly correlated with the prognosis of cancer patients. Subsequent scRNA-seq analysis depicted the heterogeneous cellular ecosystems of normal liver and HCC. Hepatocytes expressing GDF15 were less differentiated in HCC, and GDF15 promoted proliferation and invasion of HCC cell lines. Compared to normal liver, the strength of crosstalk between GDF15-positive Hepatocytes and other cells was enhanced in tumors, especially cancer-associated fibroblasts (CAFs)-derived Periostin and GDF15-positive Hepatocytes both regulate each other and jointly promote hepatocarcinogenesis. Further spatial transcriptomic data showed that GDF15 expression was negatively correlated with immune infiltration, especially in M1-type macrophages. Notably, validation analyses in bulk RNA-seq consistently emphasized the clinical significance of these findings. This study provides a comprehensive overview of the oncogenic role of the GDF subfamily in a wide range of tumors, highlights the important role of GDF15 in HCC ecosystem, and provides important biomarkers and potential therapeutic targets for future research.

Cell & BioscienceVol. 15(1)
Anhui Medical University (CN), Peking University (CN), Chinese PLA General Hospital (CN), JiangSu Armed Police General Hospital (CN), Chaohu Hospital of Anhui Medical University (CN), First Affiliated Hospital of Anhui Medical University (CN), Second Affiliated Hospital of Anhui Medical University (CN), Ningbo University Affiliated Hospital (CN), Ningbo First Hospital (CN)
Good health and well-being
Openalex Percentile: Top 75%
GDF15 and Related Biomarkers
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