Gamma-aminobutyric acid transaminase mediates tumor suppression in renal cell carcinoma through the cGAS-STING–interferon-β axis

Clear cell renal cell carcinoma (ccRCC) is resistant to conventional radiotherapy and chemotherapy, creating an urgent need for novel therapeutic strategies. Although GABA transaminase (ABAT) is involved in metabolic reprogramming as reported, its precise function and molecular mechanisms in ccRCC remain unclear. Here, we demonstrate that ABAT overexpression suppresses tumor growth both in vitro and in vivo. Mechanistically, ABAT mediates the cGAS-STING signaling pathway, and interacts with protein arginine methyltransferase 5 (PRMT5), thereby enhances interferon signaling. Besides, ABAT was found to reduce the infiltration of regulatory T cells within the tumor microenvironment. Collectively, these results suggest that ABAT represents a potential therapeutic target in clear cell renal cell carcinoma.

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Publication Details

Journal
Scientific Reports
Published
2026-03-11
DOI
https://doi.org/10.1038/s41598-026-42861-w
Primary Topic
interferon and immune responses
Type
article
Field-Weighted Citation Impact
0.00

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article

Gamma-aminobutyric acid transaminase mediates tumor suppression in renal cell carcinoma through the cGAS-STING–interferon-β axis

HongZhao Li, Senming Cao, Tianwei Cai, Chunyu Liu et al.
Scientific Reports
interferon and immune responses
article

Gamma-aminobutyric acid transaminase mediates tumor suppression in renal cell carcinoma through the cGAS-STING–interferon-β axis

HongZhao Li, Senming Cao, Tianwei Cai, Chunyu Liu, Ji Feng, Jinlu Tang, Zheng Wang, Yin Lu, Zexuan Lv, Qi Wang, Fan Gao, Yi Feng, Bin Jiang, Wenmei Fan, Xupeng Zhao, Qiang Cheng, Qing Ai
article en

Abstract

Clear cell renal cell carcinoma (ccRCC) is resistant to conventional radiotherapy and chemotherapy, creating an urgent need for novel therapeutic strategies. Although GABA transaminase (ABAT) is involved in metabolic reprogramming as reported, its precise function and molecular mechanisms in ccRCC remain unclear. Here, we demonstrate that ABAT overexpression suppresses tumor growth both in vitro and in vivo. Mechanistically, ABAT mediates the cGAS-STING signaling pathway, and interacts with protein arginine methyltransferase 5 (PRMT5), thereby enhances interferon signaling. Besides, ABAT was found to reduce the infiltration of regulatory T cells within the tumor microenvironment. Collectively, these results suggest that ABAT represents a potential therapeutic target in clear cell renal cell carcinoma.

Scientific Reports
Nankai University (CN), Chinese PLA General Hospital (CN), PLA Academy of Military Science (CN)
Ministry of Science and Technology of the People's Republic of China
Good health and well-being
Openalex Percentile: Top 25%
interferon and immune responses
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