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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.
- 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.)
- Subjects :
- Animals
Apoptosis
Biomarkers, Tumor genetics
Case-Control Studies
Cell Movement
Cell Proliferation
DNA Copy Number Variations
Female
Follow-Up Studies
Gene Expression Profiling
Gene Expression Regulation, Neoplastic
Genomics
Head and Neck Neoplasms drug therapy
Head and Neck Neoplasms genetics
Humans
Mice
Mice, Inbred BALB C
Mice, Nude
Nanomedicine
Nanoparticles chemistry
Prognosis
Prospective Studies
Squamous Cell Carcinoma of Head and Neck drug therapy
Squamous Cell Carcinoma of Head and Neck genetics
Survival Rate
Tumor Cells, Cultured
Xenograft Model Antitumor Assays
Biomarkers, Tumor metabolism
Genes, Tumor Suppressor
Head and Neck Neoplasms pathology
MicroRNAs administration & dosage
MicroRNAs genetics
Nanoparticles administration & dosage
Squamous Cell Carcinoma of Head and Neck secondary
Subjects
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