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Erschienen in: Tumor Biology 9/2016

20.07.2016 | Original Article

Expression profiles of miR-29c, miR-200b and miR-375 in tumour and tumour-adjacent tissues of head and neck cancers

verfasst von: Kristyna Hudcova, Martina Raudenska, Jaromir Gumulec, Hana Binkova, Zuzana Horakova, Rom Kostrica, Petr Babula, Vojtech Adam, Michal Masarik

Erschienen in: Tumor Biology | Ausgabe 9/2016

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Abstract

Altered expression of microRNAs (miRNAs) has been shown in many types of malignancies including the head and neck squamous cell carcinoma (HNSCC). Although there are many new and innovative approaches in the treatment of HNSCC, a clear marker of this disease is still missing. Three candidate miRNAs (miR-29c-3p, miR-200b-5p and miR-375-3p) were studied in connection with HNSCC using quantitative real-time PCR expression levels in 42 tissue samples of HNSCC patients and histologically normal tumour-adjacent tissue samples of these patients. Primary HNSCC carcinoma tissues can be distinguished from histologically normal-matched noncancerous tumour-adjacent tissues based on hsa-miR-375-3p expression (sensitivity 87.5 %, specificity 65 %). Additionally, a significant decrease of hsa-miR-200b-5p expression was revealed in tumour-adjacent tissue samples of patients with node positivity. Lower expression of hsa-miR-200b-5p and hsa-miR-29c-3p in HNSCC tumour tissue was associated with higher tumour grade. Consequently, survival analysis was performed. Lower expression of hsa-miR-29c-3p in tumour-adjacent tissue was associated with worse overall and disease-specific survivals. Lower expression of miR-29c-3p in tumourous tissue was associated with worse relapse-free survival. hsa-miR-375-3p seems to be a relatively promising diagnostic marker in HNSCC but is not suitable for prognosis of patients. Furthermore, this study highlighted the importance of histologically normal tumour-adjacent tissue in HNSCC progress (significant decrease of hsa-miR-200b-5p expression in tumour-adjacent tissue of patients with node positivity and low expression of hsa-miR-29c-3p in HNSCC tumour-adjacent tissue associated with worse prognosis).
Literatur
4.
Zurück zum Zitat Lan H, Lu H, Wang X, Jin H. MicroRNAs as potential biomarkers in cancer: opportunities and challenges. Biomed Research International. 2015:125094. doi:10.1155/2015/125094. Lan H, Lu H, Wang X, Jin H. MicroRNAs as potential biomarkers in cancer: opportunities and challenges. Biomed Research International. 2015:125094. doi:10.​1155/​2015/​125094.
7.
Zurück zum Zitat Schmitt MJ, Margue C, Behrmann I, Kreis S. miRNA-29: a microRNA family with tumor-suppressing and immune-modulating properties. Curr Mol Med. 2013;13(4):572–85.CrossRefPubMed Schmitt MJ, Margue C, Behrmann I, Kreis S. miRNA-29: a microRNA family with tumor-suppressing and immune-modulating properties. Curr Mol Med. 2013;13(4):572–85.CrossRefPubMed
8.
Zurück zum Zitat Bae HJ, Noh JH, Kim JK, Eun JW, Jung KH, Kim MG, et al. MicroRNA-29c functions as a tumor suppressor by direct targeting oncogenic SIRT1 in hepatocellular carcinoma. Oncogene. 2014;33(20):2557–67. doi:10.1038/onc.2013.216.CrossRefPubMed Bae HJ, Noh JH, Kim JK, Eun JW, Jung KH, Kim MG, et al. MicroRNA-29c functions as a tumor suppressor by direct targeting oncogenic SIRT1 in hepatocellular carcinoma. Oncogene. 2014;33(20):2557–67. doi:10.​1038/​onc.​2013.​216.CrossRefPubMed
10.
Zurück zum Zitat Zou YK, Li JW, Chen ZY, Li XW, Zheng SG, Yi D, et al. miR-29c suppresses pancreatic cancer liver metastasis in an orthotopic implantation model in nude mice and affects survival in pancreatic cancer patients. Carcinogenesis. 2015;36(6):676–84. doi:10.1093/carcin/bgv027.CrossRefPubMed Zou YK, Li JW, Chen ZY, Li XW, Zheng SG, Yi D, et al. miR-29c suppresses pancreatic cancer liver metastasis in an orthotopic implantation model in nude mice and affects survival in pancreatic cancer patients. Carcinogenesis. 2015;36(6):676–84. doi:10.​1093/​carcin/​bgv027.CrossRefPubMed
11.
13.
Zurück zum Zitat Diaz-Martin J, Diaz-Lopez A, Moreno-Bueno G, Castilla MA, Rosa-Rosa JM, Cano A, et al. A core microRNA signature associated with inducers of the epithelial-to-mesenchymal transition. J Pathol. 2014;232(3):319–29. doi:10.1002/path.4289.CrossRefPubMed Diaz-Martin J, Diaz-Lopez A, Moreno-Bueno G, Castilla MA, Rosa-Rosa JM, Cano A, et al. A core microRNA signature associated with inducers of the epithelial-to-mesenchymal transition. J Pathol. 2014;232(3):319–29. doi:10.​1002/​path.​4289.CrossRefPubMed
14.
Zurück zum Zitat Rhodes LV, Martin EC, Segar HC, Miller DF, Buechlein A, Rusch DB, et al. Dual regulation by microRNA-200b-3p and microRNA-200b-5p in the inhibition of epithelial-to-mesenchymal transition in triple-negative breast cancer. Oncotarget. 2015;6(18):16638–52. doi:10.18632/oncotarget.3184.CrossRefPubMedPubMedCentral Rhodes LV, Martin EC, Segar HC, Miller DF, Buechlein A, Rusch DB, et al. Dual regulation by microRNA-200b-3p and microRNA-200b-5p in the inhibition of epithelial-to-mesenchymal transition in triple-negative breast cancer. Oncotarget. 2015;6(18):16638–52. doi:10.​18632/​oncotarget.​3184.CrossRefPubMedPubMedCentral
22.
27.
Zurück zum Zitat Tang X, Hou Y, Yang G, Wang X, Tang S, Du YE, et al. Stromal miR-200s contribute to breast cancer cell invasion through CAF activation and ECM remodeling. Cell Death Differ. 2016;23(1):132–45. doi:10.1038/cdd.2015.78.CrossRefPubMed Tang X, Hou Y, Yang G, Wang X, Tang S, Du YE, et al. Stromal miR-200s contribute to breast cancer cell invasion through CAF activation and ECM remodeling. Cell Death Differ. 2016;23(1):132–45. doi:10.​1038/​cdd.​2015.​78.CrossRefPubMed
32.
Zurück zum Zitat Matamala N, Teresa Vargas M, Gonzalez-Campora R, Minambres R, Ignacio Arias J, Menendez P, et al. Tumor microRNA expression profiling identifies circulating microRNAs for early breast cancer detection. Clin Chem. 2015;61(8):1098–106. doi:10.1373/clinchem.2015.238691.CrossRefPubMed Matamala N, Teresa Vargas M, Gonzalez-Campora R, Minambres R, Ignacio Arias J, Menendez P, et al. Tumor microRNA expression profiling identifies circulating microRNAs for early breast cancer detection. Clin Chem. 2015;61(8):1098–106. doi:10.​1373/​clinchem.​2015.​238691.CrossRefPubMed
Metadaten
Titel
Expression profiles of miR-29c, miR-200b and miR-375 in tumour and tumour-adjacent tissues of head and neck cancers
verfasst von
Kristyna Hudcova
Martina Raudenska
Jaromir Gumulec
Hana Binkova
Zuzana Horakova
Rom Kostrica
Petr Babula
Vojtech Adam
Michal Masarik
Publikationsdatum
20.07.2016
Verlag
Springer Netherlands
Erschienen in
Tumor Biology / Ausgabe 9/2016
Print ISSN: 1010-4283
Elektronische ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-016-5147-2

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