Tumor-derived exosomal miR-619-5p promotes tumor angiogenesis and metastasis through the inhibition of RCAN1.4.

Abstract:

:Tumor-derived exosomes (TEXs) contain enriched miRNAs that act as novel non-invasive biomarkers for cancer diagnosis and play a role in cancer progression. We investigated the exosomal miRNAs that affect cancer progression in non-small cell lung cancer (NSCLC) and identified the specific molecules involved. We identified that specific miRNAs in NSCLC cell-released exosomes can modulate angiogenesis, among which miR-619-5p was the most potent inducer. RCAN1.4 was identified as a target of miR-619-5p and its suppression promoted angiogenesis. Furthermore, the suppression of RCAN1.4 induced cell proliferation and metastasis in NSCLC cells. In patients with NSCLC, the level of RCAN1.4 expression was significantly lower, and that of miR-619-5p significantly higher, in tumor than normal lung tissues. miR-619-5p expression was higher than normal in exosomes isolated from the plasma of NSCLC patients. Finally, hypoxic conditions induced miR-619-5p upload into NSCLC cell-derived exosomes. Our findings indicate that exosomal miR-619-5p promotes the growth and metastasis of NSCLCs by regulating RCAN1.4 and can serve as a diagnostic indicator for these lung cancers.

journal_name

Cancer Lett

journal_title

Cancer letters

authors

Kim DH,Park S,Kim H,Choi YJ,Kim SY,Sung KJ,Sung YH,Choi CM,Yun M,Yi YS,Lee CW,Kim SY,Lee JC,Rho JK

doi

10.1016/j.canlet.2020.01.023

subject

Has Abstract

pub_date

2020-04-10 00:00:00

pages

2-13

eissn

0304-3835

issn

1872-7980

pii

S0304-3835(20)30037-9

journal_volume

475

pub_type

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