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

IF 5.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Guanglei Shang, Wenju Zhang, Yanjie Jia, Donglei Ji, Enwei Wei, Chunfeng Gao, Caroline Zeng, Chunyu Wang, Nan Liu, Pengfei Ge, Yunqian Li, Lei Zeng
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引用次数: 0

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.

GAS41促进itga4介导的PI3K/Akt/mTOR信号通路和胶质瘤的发生。
胶质瘤扩增序列41 (Glioma Amplified Sequence 41, GAS41)是一种染色质相关蛋白,属于YEATS结构域蛋白家族,在各种肿瘤中经常被扩增。然而,其在胶质瘤中的生物学功能和致癌机制尚不完全清楚。在本研究中,我们发现GAS41在人胶质瘤组织和细胞系中表达上调,GAS41的高表达与不良临床预后显著相关。基因缺失和化学抑制可显著抑制胶质瘤细胞的增殖和转移能力,诱导细胞凋亡。此外,功能注释发现GAS41参与刺激膜蛋白ITGA4的表达,激活胶质瘤细胞系下游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具有有效的抗增殖活性。分子对接发现,这些化合物与GAS41 YEATS结构域口袋结合的方式与化合物9和3b相似,为探索GAS41选择性抑制的基本分子框架提供了结构基础。总的来说,我们的研究说明了GAS41在胶质瘤进展和恶性表型中的关键作用,并表明靶向GAS41可能是一种有希望的胶质瘤治疗策略。
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来源期刊
Biochemical pharmacology
Biochemical pharmacology 医学-药学
CiteScore
10.30
自引率
1.70%
发文量
420
审稿时长
17 days
期刊介绍: Biochemical Pharmacology publishes original research findings, Commentaries and review articles related to the elucidation of cellular and tissue function(s) at the biochemical and molecular levels, the modification of cellular phenotype(s) by genetic, transcriptional/translational or drug/compound-induced modifications, as well as the pharmacodynamics and pharmacokinetics of xenobiotics and drugs, the latter including both small molecules and biologics. The journal''s target audience includes scientists engaged in the identification and study of the mechanisms of action of xenobiotics, biologics and drugs and in the drug discovery and development process. All areas of cellular biology and cellular, tissue/organ and whole animal pharmacology fall within the scope of the journal. Drug classes covered include anti-infectives, anti-inflammatory agents, chemotherapeutics, cardiovascular, endocrinological, immunological, metabolic, neurological and psychiatric drugs, as well as research on drug metabolism and kinetics. While medicinal chemistry is a topic of complimentary interest, manuscripts in this area must contain sufficient biological data to characterize pharmacologically the compounds reported. Submissions describing work focused predominately on chemical synthesis and molecular modeling will not be considered for review. While particular emphasis is placed on reporting the results of molecular and biochemical studies, research involving the use of tissue and animal models of human pathophysiology and toxicology is of interest to the extent that it helps define drug mechanisms of action, safety and efficacy.
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