A STT3A-dependent PD-L1 glycosylation modification mediated by GMPS drives tumor immune evasion in hepatocellular carcinoma.

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Tác giả: Cheng Cheng, Qi Chu, Tianming Cui, Shumin Deng, Yumin Fu, Xinyu Guo, Changyong Ji, Xianying Li, Shuhang Liang, Lianxin Liu, Yao Liu, Yufeng Liu, Kun Ma, Linmao Sun, Jiabei Wang, Chenghui Wu, Changjian Xing, Ning Zhang, Shuo Zhou, Yitong Zhu

Ngôn ngữ: eng

Ký hiệu phân loại: 333.8232 Subsurface resources

Thông tin xuất bản: England : Cell death and differentiation , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 751427

Hepatocellular carcinoma (HCC) is a malignant tumor characterized by rapid progression. To explore the regulatory mechanism of rapid tumor growth and metastasis, we conducted proteomic and scRNA-Seq analyses on advanced HCC tissues and identified a significant molecule, guanine monophosphate synthase (GMPS), closely associated with the immune evasion in HCC. We analyzed the immune microenvironment characteristics remodeled by GMPS using scRNA-Seq and found GMPS induced tumor immune evasion in HCC by impairing the tumor-killing function of CD8
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