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GAS41促进ITGA4介导的PI3K/Akt/mTOR信号通路及胶质瘤的肿瘤发生。

GAS41 promotes ITGA4-mediated PI3K/Akt/mTOR signaling pathway and glioma tumorigenesis.

作者信息

Shang Guanglei, Zhang Wenju, Jia Yanjie, Ji Donglei, Wei Enwei, Gao Chunfeng, Zeng Caroline, Wang Chunyu, Liu Nan, Ge Pengfei, Li Yunqian, Zeng Lei

机构信息

Bethune Institute of Epigenetic Medicine, The First Hospital of Jilin University, Changchun, Jilin 130021, China; International Center of Future Science, Jilin University, Changchun, 130012, China.

Bethune Institute of Epigenetic Medicine, The First Hospital of Jilin University, Changchun, Jilin 130021, China.

出版信息

Biochem Pharmacol. 2025 Mar;233:116747. doi: 10.1016/j.bcp.2025.116747. Epub 2025 Jan 7.

Abstract

Glioma Amplified Sequence 41 (GAS41) is a chromatin-associated protein that belongs to the YEATS domain family of proteins and is frequently amplified in various tumors. However, its biological function and carcinogenic mechanism in gliomas are not fully understood. In this study, we revealed that GAS41 was upregulated in human glioma tissues and cell lines, and higher expression of GAS41 was significantly associated with poor clinical prognosis. Genetic depletion and chemical inhibition of GAS41 remarkably inhibited glioma cell proliferation and metastasis abilities and induced cellular apoptosis. Furthermore, functional annotation identified that GAS41 was involved in stimulating the expression of membrane protein ITGA4 to activate the downstream PI3K/Akt/mTOR signaling pathway in glioma cell lines. In addition, we synthesized and evaluated a series of small molecules targeting the GAS41 YEATS domain, which yielded effective anti-proliferative activities in glioma cells. Molecular docking revealed that these compounds bound to the GAS41 YEATS domain pocket in a manner similar to Compounds 9 and 3b, providing a structural basis for exploring the selective inhibition of GAS41 as part of an essential molecular framework. Overall, our study illustrates the crucial role of GAS41 in glioma progression and the malignant phenotype and suggests that targeting GAS41 may be a promising therapeutic treatment strategy for gliomas.

摘要

胶质瘤扩增序列41(GAS41)是一种与染色质相关的蛋白质,属于YEATS结构域蛋白家族,在各种肿瘤中经常发生扩增。然而,其在胶质瘤中的生物学功能和致癌机制尚未完全明确。在本研究中,我们发现GAS41在人类胶质瘤组织和细胞系中上调,且GAS41的高表达与不良临床预后显著相关。对GAS41进行基因敲除和化学抑制可显著抑制胶质瘤细胞的增殖和转移能力,并诱导细胞凋亡。此外,功能注释表明GAS41参与刺激膜蛋白ITGA4的表达,以激活胶质瘤细胞系中的下游PI3K/Akt/mTOR信号通路。此外,我们合成并评估了一系列靶向GAS41 YEATS结构域的小分子,这些小分子在胶质瘤细胞中产生了有效的抗增殖活性。分子对接显示,这些化合物以类似于化合物9和3b的方式与GAS41 YEATS结构域口袋结合,为探索作为重要分子框架一部分的GAS41的选择性抑制提供了结构基础。总体而言,我们的研究阐明了GAS41在胶质瘤进展和恶性表型中的关键作用,并表明靶向GAS41可能是一种有前景的胶质瘤治疗策略。

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