MiR-126 in intestinal-type sinonasal adenocarcinomas: exosomal transfer of MiR-126 promotes anti-tumour responses
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
1/2011/5/n.1
National Institute for Insurance against Workplace Accidents and Occupational Disease
16-31704A
Czech Health Research Council
PubMed
30223817
PubMed Central
PMC6142309
DOI
10.1186/s12885-018-4801-z
PII: 10.1186/s12885-018-4801-z
Knihovny.cz E-zdroje
- Klíčová slova
- Biomarker, Exosomes, Inflammatory polyps, Intestinal-type sinonasal adenocarcinomas, MiR-126, MiR-based therapy, Sinonasal-inverted papillomas,
- MeSH
- adenokarcinom genetika patologie terapie MeSH
- dospělí MeSH
- dřevo škodlivé účinky MeSH
- exozómy genetika metabolismus MeSH
- keratin-20 genetika MeSH
- lidé středního věku MeSH
- lidé MeSH
- mikro RNA aplikace a dávkování genetika MeSH
- nádorové biomarkery genetika MeSH
- nádory nosu genetika patologie terapie MeSH
- nádory vedlejších dutin nosních genetika patologie terapie MeSH
- patologická angiogeneze genetika terapie MeSH
- proliferace buněk genetika MeSH
- regulace genové exprese u nádorů genetika MeSH
- senioři MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- keratin-20 MeSH
- mikro RNA MeSH
- MIRN126 microRNA, human MeSH Prohlížeč
- nádorové biomarkery MeSH
BACKGROUND: Intestinal-type sinonasal adenocarcinomas (ITACs) are aggressive malignancies related to wood dust and leather exposure. ITACs are generally associated with advanced stage at presentation due to the insidious growth pattern and non-specific symptoms. Therefore, biomarkers that can detect the switch from the benign disease to malignancy are needed. Essential for tumour growth, angiogenesis is an important step in tumour development and progression. This process is strictly regulated, and MiR-126 considered its master modulator. METHODS: We have investigated MiR-126 levels in ITACs and compared them to benign sinonasal lesions, such as sinonasal-inverted papillomas (SIPs) and inflammatory polyps (NIPs). The tumour-suppressive functions of MiR-126 were also evaluated. RESULTS: We found that MiR-126 can significantly distinguish malignancy from benign nasal forms. The low levels of MiR-126 in ITACs point to its role in tumour progression. In this context, restoration of MiR-126 induced metabolic changes, and inhibited cell growth and the tumorigenic potential of MNSC cells. CONCLUSIONS: We report that MiR-126 delivered via exosomes from endothelial cells promotes anti-tumour responses. This paracrine transfer of MiRs may represent a new approach towards MiR-based therapy.
Department of Biomolecular Sciences University of Urbino Carlo Bo Urbino PU Italy
Institute of Biotechnology Czech Academy of Sciences Prague West Czech Republic
International Society of Doctors for the Environment Arezzo Italy
School of Medical Science Griffith University Southport Australia
Surgical Department ENT Metropolitan Unit Bellaria and Budrio Hospital Bologna Italy
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