Proteomic analysis reveals G0S2 as a potential apoptosis regulator in hepatocellular carcinoma

The G0/G1 switch gene 2 (G0S2) is a compact protein with diverse functions, including its involvement in apoptosis, metabolism, and inflammation. Its potential role in cancer-related apoptosis remains poorly understood. This study aimed to investigate the underlying mechanisms of G0S2 in apoptosis, particularly in cancer. Proteomic analysis was performed on G0S2-overexpressing mice, and functional annotations, pathway analysis, and protein-protein interactions were explored. Apoptosis was verified through TUNEL staining, immunohistochemistry, and molecular genetic strategies. G0S2 overexpression led to significant alterations in the expression of apoptosis-related proteins, including Caspase3, FADD, and BAX. Mechanistically, G0S2 promotes apoptosis through the BAX/Caspase3 pathway. G0S2 is implicated in apoptosis, specifically through the BAX/Caspase3 pathway, shedding light on its potential as a therapeutic target for diseases related to apoptosis, inflammation, and cancer. These findings may have implications for the development of novel therapeutic strategies for treating this devastating malignancy.

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Journal
BMC Cancer
Published
2026-09-21
DOI
https://doi.org/10.1186/s12885-026-16746-0
Primary Topic
PI3K/AKT/mTOR signaling in cancer
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article
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article

Proteomic analysis reveals G0S2 as a potential apoptosis regulator in hepatocellular carcinoma

Shizhan Ma, Yaxin Qiu, Wenxiu Sun, Mengzhe Jing et al.
BMC Cancer
PI3K/AKT/mTOR signaling in cancer
article

Proteomic analysis reveals G0S2 as a potential apoptosis regulator in hepatocellular carcinoma

Shizhan Ma, Yaxin Qiu, Wenxiu Sun, Mengzhe Jing, Mingliang Sun, Zhenyuan Zhang, Xiujuan Zhang, Yong Yan, Qi Wang, Dongming Wu
article en

Abstract

The G0/G1 switch gene 2 (G0S2) is a compact protein with diverse functions, including its involvement in apoptosis, metabolism, and inflammation. Its potential role in cancer-related apoptosis remains poorly understood. This study aimed to investigate the underlying mechanisms of G0S2 in apoptosis, particularly in cancer. Proteomic analysis was performed on G0S2-overexpressing mice, and functional annotations, pathway analysis, and protein-protein interactions were explored. Apoptosis was verified through TUNEL staining, immunohistochemistry, and molecular genetic strategies. G0S2 overexpression led to significant alterations in the expression of apoptosis-related proteins, including Caspase3, FADD, and BAX. Mechanistically, G0S2 promotes apoptosis through the BAX/Caspase3 pathway. G0S2 is implicated in apoptosis, specifically through the BAX/Caspase3 pathway, shedding light on its potential as a therapeutic target for diseases related to apoptosis, inflammation, and cancer. These findings may have implications for the development of novel therapeutic strategies for treating this devastating malignancy.

BMC Cancer
Shandong University of Traditional Chinese Medicine (CN), Fourth People’s Hospital of Jinan (CN), Shandong Provincial Hospital (CN), Taishan University (CN), Tianjin Hospital (CN), Affiliated Hospital of Shandong University of Traditional Chinese Medicine (CN), Jinan City People's Hospital (CN), Shandong First Medical University (CN)
Good health and well-being
Openalex Percentile: Top 18%
PI3K/AKT/mTOR signaling in cancer
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Proteomic analysis reveals G0S2 as a potential apoptosis regulator in hepatocellular carcinoma — Shizhan Ma, Yaxin Qiu, et al. · BMC Cancer (2026) | TGRS Research Map | TGRS