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GSK3α 调控氨基酸饥饿时癌细胞核糖体蛋白的动态变化。

GSK3α Regulates Temporally Dynamic Changes in Ribosomal Proteins upon Amino Acid Starvation in Cancer Cells.

机构信息

Department of Pediatric Hematology and Oncology, Hannover Medical School, 30625 Hannover, Germany.

Institute of Clinical Molecular Biology, Kiel University, 24105 Kiel, Germany.

出版信息

Int J Mol Sci. 2023 Aug 26;24(17):13260. doi: 10.3390/ijms241713260.

DOI:10.3390/ijms241713260
PMID:37686063
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10488213/
Abstract

Amino acid availability is crucial for cancer cells' survivability. Leukemia and colorectal cancer cells have been shown to resist asparagine depletion by utilizing GSK3-dependent proteasomal degradation, termed the Wnt-dependent stabilization of proteins (Wnt/STOP), to replenish their amino acid pool. The inhibition of GSK3α halts the sourcing of amino acids, which subsequently leads to cancer cell vulnerability toward asparaginase therapy. However, resistance toward GSK3α-mediated protein breakdown can occur, whose underlying mechanism is poorly understood. Here, we set out to define the mechanisms driving dependence toward this degradation machinery upon asparagine starvation in cancer cells. We show the independence of known stress response pathways including the integrated stress response mediated with GCN2. Additionally, we demonstrate the independence of changes in cell cycle progression and expression levels of the asparagine-synthesizing enzyme ASNS. Instead, RNA sequencing revealed that GSK3α inhibition and asparagine starvation leads to the temporally dynamic downregulation of distinct ribosomal proteins, which have been shown to display anti-proliferative functions. Using a CRISPR/Cas9 viability screen, we demonstrate that the downregulation of these specific ribosomal proteins can rescue cell death upon GSK3α inhibition and asparagine starvation. Thus, our findings suggest the vital role of the previously unrecognized regulation of ribosomal proteins in bridging GSK3α activity and tolerance of asparagine starvation.

摘要

氨基酸的可用性对癌细胞的存活至关重要。研究表明,白血病和结直肠癌细胞通过利用 GSK3 依赖性蛋白酶体降解(称为 Wnt 依赖性蛋白稳定(Wnt/STOP))来抵抗天冬酰胺耗竭,从而补充其氨基酸池。GSK3α 的抑制阻止了氨基酸的来源,这随后导致癌细胞对天冬酰胺酶治疗的敏感性。然而,可能会发生对 GSK3α 介导的蛋白分解的抵抗,其潜在机制尚不清楚。在这里,我们着手定义在天冬酰胺饥饿的癌细胞中依赖这种降解机制的机制。我们表明,包括 GCN2 介导的综合应激反应在内的已知应激反应途径的独立性。此外,我们证明了细胞周期进程的变化和天冬酰胺合成酶 ASNS 的表达水平的独立性。相反,RNA 测序显示,GSK3α 抑制和天冬酰胺饥饿导致不同核糖体蛋白的时空动态下调,这些核糖体蛋白已显示出具有抗增殖功能。使用 CRISPR/Cas9 存活筛选,我们证明这些特定核糖体蛋白的下调可以挽救 GSK3α 抑制和天冬酰胺饥饿时的细胞死亡。因此,我们的发现表明,以前未被认识到的核糖体蛋白的调节在连接 GSK3α 活性和对天冬酰胺饥饿的耐受性方面起着至关重要的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a0/10488213/096192f6972f/ijms-24-13260-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a0/10488213/7041a1e32725/ijms-24-13260-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a0/10488213/6469d543327e/ijms-24-13260-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a0/10488213/f78720384bc1/ijms-24-13260-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a0/10488213/c3a1de527513/ijms-24-13260-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a0/10488213/096192f6972f/ijms-24-13260-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a0/10488213/7041a1e32725/ijms-24-13260-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a0/10488213/6469d543327e/ijms-24-13260-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a0/10488213/f78720384bc1/ijms-24-13260-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a0/10488213/096192f6972f/ijms-24-13260-g005.jpg

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