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Long non‐coding RNA HOTAIR/microRNA‐206 sponge regulates STC2 and further influences cell biological functions in head and neck squamous cell carcinoma
Long non‐coding RNA HOTAIR/microRNA‐206 sponge regulates STC2 and further influences cell biological functions in head and neck squamous cell carcinoma
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Long non‐coding RNA HOTAIR/microRNA‐206 sponge regulates STC2 and further influences cell biological functions in head and neck squamous cell carcinoma
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Long non‐coding RNA HOTAIR/microRNA‐206 sponge regulates STC2 and further influences cell biological functions in head and neck squamous cell carcinoma
Long non‐coding RNA HOTAIR/microRNA‐206 sponge regulates STC2 and further influences cell biological functions in head and neck squamous cell carcinoma

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Long non‐coding RNA HOTAIR/microRNA‐206 sponge regulates STC2 and further influences cell biological functions in head and neck squamous cell carcinoma
Long non‐coding RNA HOTAIR/microRNA‐206 sponge regulates STC2 and further influences cell biological functions in head and neck squamous cell carcinoma
Journal Article

Long non‐coding RNA HOTAIR/microRNA‐206 sponge regulates STC2 and further influences cell biological functions in head and neck squamous cell carcinoma

2019
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Overview
Objective It is essential to characterize underlying molecular mechanism associated with head and neck squamous cell carcinoma (HNSCC) and identify promising therapeutic targets. Herein, we explored role of homeobox transcript antisense RNA (HOTAIR) in HNSCC to regulate stanniocalcin‐2 (STC2) by sponging microRNA‐206 (miR‐206). Methods HNSCC‐related differentially expressed genes and regulation network amongst HOTAIR, miR‐206 and STC2 were identified. Next, effect of HOTAIR on cell biological functions of HNSCC was identified after transfection of cells with HOTAIR overexpressed plasmids or siRNA against HOTAIR. PI3K/AKT signalling pathway‐related gene expression was measured after miR‐206 and STC2 were suppressed. Cell invasion, migration and proliferation were assessed. Finally, tumour growth was assessed to determine the effects of HOTAIR/miR‐206/STC2 axis in vivo. Results HOTAIR specifically bound to miR‐206 and miR‐206 targeted STC2. Downregulated HOTAIR or upregulated miR‐206 suppressed HNSCC cell proliferation, invasion and migration. miR‐206 inhibited PI3K/AKT signalling pathway by down‐regulating STC2. Besides, silenced HOTAIR or overexpressed miR‐206 repressed the tumour growth of nude mice with HNSCC. Conclusion HOTAIR regulated HNSCC cell biological functions by binding to miR‐206 through STC2.
Publisher
John Wiley & Sons, Inc,John Wiley and Sons Inc
Subject

1-Phosphatidylinositol 3-kinase

/ AKT protein

/ Animals

/ Antibodies

/ Antisense RNA

/ Apoptosis

/ Cell Line, Tumor

/ Cell migration

/ Cell Movement

/ Cell Proliferation

/ Cells

/ Female

/ Gastric cancer

/ Gene expression

/ Gene Expression Regulation, Neoplastic

/ Gene regulation

/ Glycoproteins - antagonists & inhibitors

/ Glycoproteins - genetics

/ Glycoproteins - metabolism

/ Head and neck carcinoma

/ Head and Neck Neoplasms - metabolism

/ Head and Neck Neoplasms - pathology

/ head and neck squamous cell carcinoma

/ Homeobox

/ Humans

/ In vivo methods and tests

/ Intercellular Signaling Peptides and Proteins - genetics

/ Intercellular Signaling Peptides and Proteins - metabolism

/ invasion

/ Kinases

/ long non‐coding RNA homeobox transcript antisense RNA

/ Metastasis

/ Mice

/ Mice, Nude

/ MicroRNAs

/ MicroRNAs - antagonists & inhibitors

/ MicroRNAs - genetics

/ MicroRNAs - metabolism

/ microRNA‐206

/ migration

/ miRNA

/ Molecular modelling

/ Original

/ Phosphatidylinositol 3-Kinases - metabolism

/ Plasmids

/ proliferation

/ Proteins

/ Proto-Oncogene Proteins c-akt - metabolism

/ Radiation therapy

/ Ribonucleic acid

/ RNA

/ RNA Interference

/ RNA, Long Noncoding - antagonists & inhibitors

/ RNA, Long Noncoding - genetics

/ RNA, Long Noncoding - metabolism

/ RNA, Small Interfering - metabolism

/ Signal Transduction

/ Signaling

/ siRNA

/ Squamous cell carcinoma

/ Squamous Cell Carcinoma of Head and Neck - metabolism

/ Squamous Cell Carcinoma of Head and Neck - pathology

/ Stanniocalcin

/ stanniocalcin‐2

/ Therapeutic targets

/ Transfection

/ Tumorigenesis

/ Tumors