Intermittent hypoxia mediates paraspeckle protein-1 upregulation in sleep apnea

As some evidence suggests that hypoxia might be an inducer of nuclear paraspeckle formation, we explore whether intermittent hypoxia (IH)-mediated paraspeckle protein-1 (PSPC1) overexpression might contribute to the activation of tumor growth factor (TGF)β-SMAD pathway in patients with obstructive s...

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Bibliographic Details
Authors: Díaz-García, Elena; García-Tovar, Sara; Casitas, Raquel; Jaureguizar, Ana; Zamarrón, Ester; Sánchez-Sánchez, Begoña; Sastre-Perona, Ana; López-Collazo, Eduardo; García Rio, Francisco; Cubillos-Zapata, Carolina
Format: Article
Publication date:2021
Country:España
Institution:Universidad Autónoma de Madrid
Repository:Biblos-e Archivo. Repositorio Institucional de la UAM
Language:English
OAI Identifier:oai:repositorio.uam.es:10486/716560
Online Access:http://hdl.handle.net/10486/716560
https://dx.doi.org/10.3390/cancers13153888
Access Level:Open access
Keyword:HIF1α
Intermittent hypoxia
Paraspeckle component 1
Sleep apnea
TGFβ
Medicina
Description
Summary:As some evidence suggests that hypoxia might be an inducer of nuclear paraspeckle formation, we explore whether intermittent hypoxia (IH)-mediated paraspeckle protein-1 (PSPC1) overexpression might contribute to the activation of tumor growth factor (TGF)β-SMAD pathway in patients with obstructive sleep apnea (OSA). This activation would promote changes in intracellular signaling that would explain the increased cancer aggressiveness reported in these patients. Here, we show that patients with OSA exhibit elevated PSPC1 levels both in plasma and in monocytes. Our data suggest that PSPC1 is ultimately delivered to the plasma through its cleavage from OSA monocytes by matrix metalloproteinase-2 (MMP2). In addition, IH promotes PSPC1, TGFβ, and MMP2 expression in monocytes through the hypoxia-inducible factor. Lastly, both PSPC1 and TGFβ induce increased expression of genes that drive the epithelial-to-mesenchymal transition. Our study details the mechanism by which hypoxemia upmodulates the extracellular release of PSPC1 by means of MMP2, such that plasma PSPC1 together with TGFβ activation signaling further promotes tumor metastasis and supports cancer aggressiveness in patients with OSA