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PP013

Authors :
Cheng Chieh Yang
Kuo Wei Chang
Shou Yen Kao
Hsi Feng Tu
En-Hao Yu
Chung Ji Liu
Pei-Wen Wang
Shu-Chun Lin
Che-Lun Chang
Source :
Oral Oncology. 49:S97
Publication Year :
2013
Publisher :
Elsevier BV, 2013.

Abstract

MicroRNAs (miRNAs) play important roles in modulating the neoplastic process of cancers including head and neck squamous cell carcinoma (HNSCC). Purpose A genetic polymorphism (rs2292832, C > T) has been recently identified in the precursor of miR-149; nevertheless its clinicopathological implications remain obscure. Material and methods 273 HNSCC patients and 122 healthy controls were enrolled for genotyping analysis and HNSCC cell lines including SAS, OECM-1, FaDu were chosen for phenotypic assay regarding to miR-149 expression. Results We showed that miR-149 is down-regulated in HNSCC compared to normal mucosa and this is associated with a poorer patient survival. In addition, HNSCC patients with the T/T genotype have more advanced tumors and a worse prognosis. Multivariate analysis indicated that patients carried the T/T genotype have a 2.81-fold (95% CI: 1.58–4.97) increased risk of nodal metastasis and 1.66-fold (95% CI: 1.05–2.60) increased risk of mortality compared to other groups. T/T genotype also predicted the worse prognosis of buccal mucosa carcinoma subset of HNSCC. In vitro analysis indicated that exogenous miR-149 expression reduces the migration of HNSCC cells. Moreover, HNSCC cell subclones carrying the pri-mir-149 sequence containing the T variant show a low processing efficacy when converting the pre-mir-149 to mature miR-149. Conclusions These findings suggest that miR-149 suppresses tumor cell mobility, and that the pre-mir-149 polymorphism may affect the processing of miR-149, resulting in a change in the abundance of the mature form miRNA, which, in turn, modulates tumor progression and patient survival.

Details

ISSN :
13688375
Volume :
49
Database :
OpenAIRE
Journal :
Oral Oncology
Accession number :
edsair.doi...........540d3920fac5fb917a3727976b0c613e
Full Text :
https://doi.org/10.1016/j.oraloncology.2013.03.256