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AEP promotes aberrant RNA splicing through DDX3X cleavage in solid tumors
Yadong Xie, … , Haohao Zhang, Xinyang Song
Yadong Xie, … , Haohao Zhang, Xinyang Song
Published February 1, 2024
Citation Information: J Clin Invest. 2024;134(3):e177609. https://doi.org/10.1172/JCI177609.
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Commentary

AEP promotes aberrant RNA splicing through DDX3X cleavage in solid tumors

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Abstract

Aberrant alternative splicing (AS) events have been identified in a variety of cancers. Although somatic mutations of splicing factors and dysregulation of RNA-binding proteins (RBPs) have been linked to AS and tumor malignancy, it remains unclear how upstream mechanisms contribute to cancer development via alternative gene splicing. In this issue of the JCI, Wenrui Zhang and colleagues identified the role of asparagine endopeptidase (AEP), an intracellular cysteine endopeptidase, in promoting solid tumor–associated RNA splicing. The authors demonstrated that tumor environmental factors such as oxygen and nutrient deprivation induce the activity of AEP in a HIF1A-dependent manner. The activated AEP, in turn, cleaves an RNA helicase DDX3X to promote its nuclear retention. The authors further showed that this DDX3X nuclear fraction engages with splicing machinery to induce AS events in several cancer cells. These findings suggest that targeting an AEP-dependent aberrant RNA splicing cascade may facilitate therapeutics for solid tumors.

Authors

Yadong Xie, Haohao Zhang, Xinyang Song

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Figure 1

AEP cleaves DDX3X to drive tumor-promoting AS events.

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AEP cleaves DDX3X to drive tumor-promoting AS events.
Tumor microenviron...
Tumor microenvironmental stresses, such as hypoxia and nutrient deprivation, activate AEP from its inactive form (pro-AEP) into the mature form through HIF1A. AEP cleaves DDX3X at amino acid 124 to induce its nuclear translocation. Once in the nucleus, t-DDX3X-C affects downstream tumor AS events in a hnRNPA1-dependent manner. Examples of pre-mRNAs affected include transcripts that encode ARRB1, involved in the regulation of glycolysis, and PRDM2, which is important for tumor suppression.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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