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Extracellular Vesicle LincRNA-p21 Expression in Tumor-Draining Pulmonary Vein Defines Prognosis in NSCLC and Modulates Endothelial Cell Behavior

Overview
Journal Cancers (Basel)
Publisher MDPI
Specialty Oncology
Date 2020 Apr 5
PMID 32244977
Citations 28
Authors
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Abstract

Hypoxia-induced upregulation of lincRNA-p21 in tumor tissue was previously shown by our group to be related to poor prognosis in resected non-small cell lung cancer (NSCLC) patients. In the present study, we have evaluated the presence of lincRNA-p21 in extracellular vesicles (EVs) from NSCLC patients and assessed its potential as a prognostic biomarker. High EV lincRNA-p21 levels in blood from the tumor-draining vein were associated with shorter time to relapse and shorter overall survival. Moreover, the multivariate analysis identified high lincRNA-p21 levels as an independent prognostic marker. In addition, lincRNA-p21 was overexpressed in H23 and HCC44 NSCLC cell lines and their derived EVs under hypoxic conditions. Functional assays using human umbilical vein endothelial cells (HUVECs) showed that tumor-derived EVs enriched in lincRNA-p21 affected endothelial cells by promoting tube formation and enhancing tumor cell adhesion to endothelial cells. Additionally, the analysis of selected EV microRNAs related to angiogenesis and metastasis showed that the microRNAs correlated with EV lincRNA-p21 levels in both patients and cell lines. Finally, EV co-culture with HUVEC cells increased the expression of microRNAs and genes related to endothelial cell activation. In conclusion, EV lincRNA-p21 acts as a novel prognosis marker in resected NSCLC patients, promoting angiogenesis and metastasis.

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References
1.
Cabili M, Trapnell C, Goff L, Koziol M, Tazon-Vega B, Regev A . Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses. Genes Dev. 2011; 25(18):1915-27. PMC: 3185964. DOI: 10.1101/gad.17446611. View

2.
Yu F, Zhou G, Huang K, Fan X, Li G, Chen B . Serum lincRNA-p21 as a potential biomarker of liver fibrosis in chronic hepatitis B patients. J Viral Hepat. 2017; 24(7):580-588. DOI: 10.1111/jvh.12680. View

3.
Shen Y, Liu Y, Sun T, Yang W . LincRNA-p21 knockdown enhances radiosensitivity of hypoxic tumor cells by reducing autophagy through HIF-1/Akt/mTOR/P70S6K pathway. Exp Cell Res. 2017; 358(2):188-198. DOI: 10.1016/j.yexcr.2017.06.016. View

4.
Gomez-Maldonado L, Tiana M, Roche O, Prado-Cabrero A, Jensen L, Fernandez-Barral A . EFNA3 long noncoding RNAs induced by hypoxia promote metastatic dissemination. Oncogene. 2014; 34(20):2609-20. PMC: 4722872. DOI: 10.1038/onc.2014.200. View

5.
Gezer U, Ozgur E, Cetinkaya M, Isin M, Dalay N . Long non-coding RNAs with low expression levels in cells are enriched in secreted exosomes. Cell Biol Int. 2014; 38(9):1076-9. DOI: 10.1002/cbin.10301. View