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Biomed Pharmacother ; 84: 722-729, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27710896

RESUMO

Aberrantly expressed microRNAs (miRNAs) are involved in many diseases including cancer. In clear cell renal cell carcinoma (ccRCCs) expression of miR-133b and miR-135a is reduced compared to control tissue and other sarcomas but the functional effects of this downregulation are not fully understood. This study aimed at evaluating the miR-133b and miR-135a expression profiles in different RCC subtypes and the functional role of these miRNAs. Viability and apoptosis were examined in three different ccRCC cell lines (786-O, A498 and SN12-PM6) after over-expression of these miRNAs. The modulation of JAK2 and the JAK2/STAT3 pathways was determined by Western blot. Transient transfection of miR-133b and miR-135a reduced viability and induced apoptosis by inhibition of JAK2 expression and its phosphorylation and activation of caspase 3 and 7 in all three ccRCC cell lines. p-STAT3 and Bcl-2 expression was reduced after miRNA transfection whereas only slight influence on Bcl-2 L11 (BIM) was detected. Our results demonstrate that miR-133b and miR-135a which are down-regulated in wildtype and mutated ccRCCs, induce apoptosis in vitro by a signaling cascade involving JAK2, STAT3 and Bcl-2. Therefore, over-expression of these miRNAs seems to functionally counteract oncogenic signalling pathways in ccRCCs.


Assuntos
Carcinoma de Células Renais/metabolismo , Janus Quinase 2/biossíntese , Neoplasias Renais/metabolismo , MicroRNAs/biossíntese , Fator de Transcrição STAT3/biossíntese , Apoptose/fisiologia , Carcinoma de Células Renais/genética , Linhagem Celular Tumoral , Humanos , Janus Quinase 2/genética , Neoplasias Renais/genética , MicroRNAs/genética , Fator de Transcrição STAT3/genética , Transdução de Sinais/fisiologia
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