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Integrated Genomic and Functional microRNA Analysis Identifies miR-30-5p as a Tumor Suppressor and Potential Therapeutic Nanomedicine in Head and Neck Cancer.

Authors :
Saleh AD
Cheng H
Martin SE
Si H
Ormanoglu P
Carlson S
Clavijo PE
Yang X
Das R
Cornelius S
Couper J
Chepeha D
Danilova L
Harris TM
Prystowsky MB
Childs GJ
Smith RV
Robertson AG
Jones SJM
Cherniack AD
Kim SS
Rait A
Pirollo KF
Chang EH
Chen Z
Van Waes C
Source :
Clinical cancer research : an official journal of the American Association for Cancer Research [Clin Cancer Res] 2019 May 01; Vol. 25 (9), pp. 2860-2873. Date of Electronic Publication: 2019 Feb 05.
Publication Year :
2019

Abstract

Purpose: To identify deregulated and inhibitory miRNAs and generate novel mimics for replacement nanomedicine for head and neck squamous cell carcinomas (HNSCC).<br />Experimental Design: We integrated miRNA and mRNA expression, copy number variation, and DNA methylation results from The Cancer Genome Atlas (TCGA), with a functional genome-wide screen.<br />Results: We reveal that the miR-30 family is commonly repressed, and all 5 members sharing these seed sequence similarly inhibit HNSCC proliferation in vitro . We uncover a previously unrecognized inverse relationship with overexpression of a network of important predicted target mRNAs deregulated in HNSCC, that includes key molecules involved in proliferation (EGFR, MET, IGF1R, IRS1, E2F7), differentiation (WNT7B, FZD2), adhesion, and invasion (ITGA6, SERPINE1). Reexpression of the most differentially repressed family member, miR-30a-5p, suppressed this mRNA program, selected signaling proteins and pathways, and inhibited cell proliferation, migration, and invasion in vitro . Furthermore, a novel miR-30a-5p mimic formulated into a targeted nanomedicine significantly inhibited HNSCC xenograft tumor growth and target growth receptors EGFR and MET in vivo . Significantly decreased miR-30a/e family expression was related to DNA promoter hypermethylation and/or copy loss in TCGA data, and clinically with decreased disease-specific survival in a validation dataset. Strikingly, decreased miR-30e-5p distinguished oropharyngeal HNSCC with poor prognosis in TCGA ( P = 0.002) and validation ( P = 0.007) datasets, identifying a novel candidate biomarker and target for this HNSCC subset.<br />Conclusions: We identify the miR-30 family as an important regulator of signal networks and tumor suppressor in a subset of HNSCC patients, which may benefit from miRNA replacement nanomedicine therapy.<br /> (©2019 American Association for Cancer Research.)

Details

Language :
English
ISSN :
1557-3265
Volume :
25
Issue :
9
Database :
MEDLINE
Journal :
Clinical cancer research : an official journal of the American Association for Cancer Research
Publication Type :
Academic Journal
Accession number :
30723145
Full Text :
https://doi.org/10.1158/1078-0432.CCR-18-0716