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子宫内膜癌 A230V-ALK5(TGFBR1)突变体减弱 TGF-β 信号传导,并表现出对 ALK5 抑制剂的体外敏感性降低。

The endometrial cancer A230V-ALK5 (TGFBR1) mutant attenuates TGF-β signaling and exhibits reduced in vitro sensitivity to ALK5 inhibitors.

机构信息

Reproductive Cancer Genetics Section, Cancer Genetics and Comparative Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America.

出版信息

PLoS One. 2024 Nov 22;19(11):e0312806. doi: 10.1371/journal.pone.0312806. eCollection 2024.

Abstract

The ALK5 (TGFBR1) receptor serine/threonine kinase transduces TGF-β (Transforming Growth Factor beta) signaling to activate SMAD2/3-dependent and -independent pathways. Here, we aimed to determine the functional consequences of ALK5 mutations in human endometrial cancer (EC). Somatic mutation data were retrieved from publicly available databases. Using seven in silico algorithms, 78.5% (11 of 14) of ALK5 kinase domain mutations in EC, including A230V-ALK5, were predicted to impact protein function. For in vitro studies, we focused on A230V-ALK5 because it was the only mutated residue located within the ATP-binding pocket, which is an important region for both ATP-binding and binding of ATP-competitive inhibitors. Constructs expressing wildtype-, constitutively-active-, kinase-dead-, or mutant A230V-ALK5, were transfected into NIH/3T3 cells. Following TGF-β1 stimulation, transient exogenous expression of A230V-ALK5 resulted in attenuated SMAD2/3 signal transduction and reduced AKT activation. We further showed that the A230V-ALK5 mutant had reduced stability resulting from increased ubiquitin-dependent protein degradation. Our structural modeling predicted that SB-431542, a small molecule ATP-competitive inhibitor of ALK5, binds to the A230V-ALK5 mutant with reduced affinity compared to wildtype-ALK5. We therefore examined the inhibitory effect of SB-431542 and galunisertib on wildtype- and mutant-ALK5 activity using a Smad-binding element (SBE) luciferase reporter assay combined with TGF-β1 stimulation, in NIH/3T3 cells and HEC-265 EC cells. SBE luciferase activity in A230V-ALK5 transfected cells was inhibited less by SB-431542 and galunisertib than in wildtype-ALK5 transfected cells indicating that A230V-ALK5 is less sensitive to inhibition by these agents than wildtype-ALK5, potentially due to changes in SB-431542/A230V-ALK5 binding affinity. Our findings are novel and show that A230V-ALK5 is a partial loss-of-function mutant that attenuates TGF-β1 signal transduction and has reduced sensitivity to ALK5 small molecule inhibitors.

摘要

ALK5(TGFBR1)受体丝氨酸/苏氨酸激酶将 TGF-β(转化生长因子β)信号转导至激活 SMAD2/3 依赖性和非依赖性途径。在这里,我们旨在确定人类子宫内膜癌(EC)中 ALK5 突变的功能后果。体细胞突变数据从公开可用的数据库中检索。使用七种计算机算法,EC 中的 ALK5 激酶结构域突变(包括 A230V-ALK5)的 78.5%(14 个中的 11 个)被预测会影响蛋白功能。对于体外研究,我们主要关注 A230V-ALK5,因为它是唯一位于 ATP 结合口袋内的突变残基,ATP 结合口袋对于 ATP 结合和 ATP 竞争性抑制剂的结合都是重要区域。表达野生型、组成型激活型、激酶失活型或突变型 A230V-ALK5 的构建体被转染到 NIH/3T3 细胞中。在 TGF-β1 刺激后,瞬时外源性表达 A230V-ALK5 导致 SMAD2/3 信号转导减弱和 AKT 激活减少。我们进一步表明,A230V-ALK5 突变体由于泛素依赖性蛋白降解增加而导致稳定性降低。我们的结构建模预测,SB-431542 是一种小分子 ALK5 的 ATP 竞争性抑制剂,与野生型 ALK5 相比,与 A230V-ALK5 突变体的结合亲和力降低。因此,我们使用 TGF-β1 刺激联合 Smad 结合元件(SBE)荧光素酶报告基因测定,在 NIH/3T3 细胞和 HEC-265 EC 细胞中检查了 SB-431542 和 galunisertib 对野生型和突变型 ALK5 活性的抑制作用。在转染 A230V-ALK5 的细胞中,SBE 荧光素酶活性对 SB-431542 和 galunisertib 的抑制作用小于转染野生型 ALK5 的细胞,表明 A230V-ALK5 对这些药物的抑制作用不如野生型 ALK5 敏感,这可能是由于 SB-431542/A230V-ALK5 结合亲和力的变化所致。我们的研究结果是新颖的,表明 A230V-ALK5 是一种部分功能丧失的突变体,可减弱 TGF-β1 信号转导,并对 ALK5 小分子抑制剂的敏感性降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af8/11584080/f893556df96c/pone.0312806.g001.jpg

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