Data/hora: 06/06/2024 19:06:56

Provedor de dados: 	56	
País: 	Brazil	
Título: 	Identification of microRNAs and mRNAs associated with multidrug resistance of human laryngeal cancer Hep-2 cells	
Autores: 	Yin,Wanzhong; Wang,Ping; Wang,Xin; Song,Wenzhi; Cui,Xiangyan; Yu,Hong; Zhu,Wei.	
Data: 	2013-06-01	
Ano: 	2013	
Palavras-chave: 	Multidrug resistance; Laryngeal cancer; Hep-2 cells; MRNA; MicroRNA.	
Resumo: 	Multidrug resistance (MDR) poses a serious impediment to the success of chemotherapy for laryngeal cancer. To identify microRNAs and mRNAs associated with MDR of human laryngeal cancer Hep-2 cells, we developed a multidrug-resistant human laryngeal cancer subline, designated Hep-2/v, by exposing Hep-2 cells to stepwise increasing concentrations of vincristine (0.02-0.96'µM). Microarray assays were performed to compare the microRNA and mRNA expression profiles of Hep-2 and Hep-2/v cells. Compared to Hep-2 cells, Hep-2/v cells were more resistant to chemotherapy drugs (∼45-fold more resistant to vincristine, 5.1-fold more resistant to cisplatin, and 5.6-fold more resistant to 5-fluorouracil) and had a longer doubling time (42.33±1.76 vs 28.75±1.12'h, P&lt;0.05), higher percentage of cells in G0/G1 phase (80.98±0.52 vs69.14±0.89, P&lt;0.05), increased efflux of rhodamine 123 (95.97±0.56 vs 12.40±0.44%, P&lt;0.01), and up-regulated MDR1 expression. A total of 7 microRNAs and 605 mRNAs were differentially expressed between the two cell types. Of the differentially expressed mRNAs identified, regulator of G-protein signaling 10, high-temperature requirement protein A1, and nuclear protein 1 were found to be the putative targets of the differentially expressed microRNAs identified. These findings may open a new avenue for clarifying the mechanisms responsible for MDR in laryngeal cancer.	
Tipo: 	Info:eu-repo/semantics/article	
Idioma: 	Inglês	
Identificador: 	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2013000600546	
Editor: 	Associação Brasileira de Divulgação Científica	
Relação: 	10.1590/1414-431X20131662	
Formato: 	text/html	
Fonte: 	Brazilian Journal of Medical and Biological Research  v.46 n.6 2013	
Fonte: 	info:eu-repo/semantics/openAccess