Sohlh1 Modulates the Stemness and Differentiation of Glioma Stem-Like Cells by Inactivation of Wnt/β-Catenin Signalling Pathway via SFRP1

IF 5.3
Sujuan Zhi, YanRu Chen, Yunling Xiao, Lanlan Liu, Xiaoning Feng, Xuyue Liu, Ying Shen, RuiHong Zhang, Jing Hao
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引用次数: 0

Abstract

Glioma stem-like cells (GSLCs) are tumour initiating cells that drive tumorigenesis and progression through self-renewal and various differentiation potencies. Therefore, the identification of genes required for GSLC stemness and differentiation is vital for the development of novel targeted therapies. Sohlh1 belongs to the superfamily of bhlh transcription factors and serves as a tumour suppressor in glioma. The role of Sohlh1 in GSLCs remains unknown. Here, we demonstrated that Sohlh1 functioned through the SFRP1/Wnt/β-catenin signalling pathway and led to the consequent suppression of GSLC stemness and the promotion of GSLC differentiation in vitro and in vivo. Moreover, Sohlh1 could directly bind to the promoter of SFRP1 and promote its transcriptional activity. SFRP1 mediated the effects of Sohlh1 on GSLC stemness and differentiation. Clinically, we observed a significant inverse correlation between Sohlh1 and Nestin expression levels, and a positive correlation between Sohlh1 and SFRP1 expression in glioma tissues. Collectively, our findings suggest an important role of the Sohlh1/SFRP1/Wnt/β-catenin pathway in regulating GSLC stemness and differentiation, suggesting potential therapeutic targets for glioma.

Sohlh1通过SFRP1失活Wnt/β-Catenin信号通路调控胶质瘤干细胞样细胞的干性和分化
胶质瘤干细胞(GSLCs)是肿瘤起始细胞,通过自我更新和各种分化能力驱动肿瘤发生和进展。因此,鉴定GSLC干细胞和分化所需的基因对于开发新的靶向治疗方法至关重要。Sohlh1属于bhlh转录因子超家族,在胶质瘤中起肿瘤抑制作用。Sohlh1在GSLCs中的作用尚不清楚。在这里,我们证明了Sohlh1通过SFRP1/Wnt/β-catenin信号通路发挥作用,并导致GSLC干性的抑制,促进GSLC在体外和体内的分化。Sohlh1可以直接结合SFRP1的启动子,促进其转录活性。SFRP1介导Sohlh1对GSLC干性和分化的影响。在临床上,我们观察到Sohlh1与Nestin表达水平呈显著负相关,而Sohlh1与SFRP1在胶质瘤组织中的表达呈正相关。总之,我们的研究结果表明Sohlh1/SFRP1/Wnt/β-catenin通路在调节GSLC的干性和分化中起重要作用,提示了胶质瘤的潜在治疗靶点。
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来源期刊
CiteScore
11.50
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0.00%
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期刊介绍: The Journal of Cellular and Molecular Medicine serves as a bridge between physiology and cellular medicine, as well as molecular biology and molecular therapeutics. With a 20-year history, the journal adopts an interdisciplinary approach to showcase innovative discoveries. It publishes research aimed at advancing the collective understanding of the cellular and molecular mechanisms underlying diseases. The journal emphasizes translational studies that translate this knowledge into therapeutic strategies. Being fully open access, the journal is accessible to all readers.
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