MicroRNA-126 suppresses proliferation of undifferentiated (BRAFV600E and BRAFWT) thyroid carcinoma through targeting PIK3R2 gene and repressing PI3K-AKT proliferation-survival signalling pathway
- 1. Cancer Molecular Pathology, School of Medicine, Menzies Health Institute Queensland, Griffith University, Gold Coast, Queensland (Australia)
- 2. Genomics Research Centre, Institute of Health and Biomedical Innovation, Faculty of Health, Queensland University of Technology, Brisbane, Queensland (Australia)
- 3. Pathology Queensland and Gold Coast University Hospital, Gold Coast, Queensland (Australia)
Description
Background: The objectives of this study are to investigate the expression of miR-126 and evaluate its effect on proliferation in undifferentiated thyroid carcinoma. Methods: miR-126 expression of undifferentiated thyroid carcinoma cell lines 8505C (BRAFV600E/V600E), BHT-101 (BRAFV600E/WT) and MB-1 (BRAFWT/WT) were quantified with q-PCR. These cell lines were transiently transfected with exogenous miR-126 (mimic). Following transfection, proliferation effects were observed through MTS proliferation assay and colony formation abilities. Immunofluorescence imaging and Western blot assay were also done to check target proteins expression. Results: Under-expression (p<0.05) of miR-126 was noted in BRAFV600E mutated undifferentiated thyroid carcinoma cells (8505C and BHT-101), but no change in expression was noted in non BRAFV600E mutated undifferentiated thyroid carcinoma cells (MB-1). In addition, a 30–50% drop in proliferation ability and a 35–45% reduction in colony formation capability were noticed in miR-126 mimic transfected group when compared to control group. Furthermore, immunofluorescence images showed reduced expression of p85β and p-AKT protein in miR-126 mimic transfected cells when compared to un-transfected cells. Also, Western blot analysis revealed a 34–40% suppression of p85β protein and a 21–53% drop in active AKT kinase (p-AKT) protein in miR-126 mimic transfected group when compared to control group. Conclusions: Expression of miR-126 was down-regulated in BRAFV600E mutated undifferentiated thyroid carcinoma. In addition, miR-126 was found to act as proliferation suppressor targeting PIK3R2 gene and reducing p85β (a regulatory subunit of PI3K kinase) protein translation and lower AKT kinase activity. Therefore, miR-126 could be a potential therapeutic tool in the treatment of undifferentiated thyroid carcinoma. - Highlights: • miR-126 expression was low in BRAF mutated undifferentiated thyroid carcinoma. • miR-126 suppresses p85β expression in undifferentiated thyroid carcinoma. • miR-126 suppresses AKT kinase activity in undifferentiated thyroid carcinoma. • miR-126 suppresses proliferation of undifferentiated thyroid carcinoma.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.yexcr.2015.09.010Additional details
Identifiers
- DOI
- 10.1016/j.yexcr.2015.09.010;
- PII
- S0014-4827(15)30093-8;
Publishing Information
- Journal Title
- Experimental Cell Research
- Journal Volume
- 339
- Journal Issue
- 2
- Journal Page Range
- p. 342-350
- ISSN
- 0014-4827
- CODEN
- ECREAL
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 49097335
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- BIOMEDICAL RADIOGRAPHY; CARCINOMAS; COLONY FORMATION; COMPARATIVE EVALUATIONS; GENES; IMAGES; INHIBITION; PHOSPHOTRANSFERASES; POLYMERASE CHAIN REACTION; THYROID; VANADIUM 60
- Descriptors DEC
- BODY; DIAGNOSTIC TECHNIQUES; DISEASES; ENDOCRINE GLANDS; ENZYMES; EVALUATION; GENE AMPLIFICATION; GLANDS; INTERMEDIATE MASS NUCLEI; ISOTOPES; MEDICINE; NEOPLASMS; NUCLEAR MEDICINE; NUCLEI; ODD-ODD NUCLEI; ORGANIC COMPOUNDS; ORGANS; PHOSPHORUS-GROUP TRANSFERASES; PROTEINS; RADIOLOGY; TRANSFERASES; VANADIUM ISOTOPES
Optional Information
- Copyright
- Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.