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Segment-specific targeting via RNA interference mediates down-regulation of OPN expression in hepatocellular carcinoma cells.
Lin, F; Huang, C M; Cao, J; Pei, Z H; Gu, W L; Fan, S F; Li, K P; Lin, C M.
Afiliação
  • Lin F; Department of General Surgery, Guangzhou First People's Hospital Affiliated to Guangzhou Medical University, Guangzhou, Guangdong, China.
  • Huang CM; Department of General Surgery, People's Hospital of Guangdong Province, Guangzhou, Guangdong, China.
  • Cao J; Department of General Surgery, Guangzhou First People's Hospital Affiliated to Guangzhou Medical University, Guangzhou, Guangdong, China caojiecn@yeah.net.
  • Pei ZH; Department of General Surgery, Guangzhou First People's Hospital Affiliated to Guangzhou Medical University, Guangzhou, Guangdong, China.
  • Gu WL; Department of General Surgery, Guangzhou First People's Hospital Affiliated to Guangzhou Medical University, Guangzhou, Guangdong, China.
  • Fan SF; Department of General Surgery, Guangzhou First People's Hospital Affiliated to Guangzhou Medical University, Guangzhou, Guangdong, China.
  • Li KP; Department of General Surgery, Guangzhou First People's Hospital Affiliated to Guangzhou Medical University, Guangzhou, Guangdong, China.
  • Lin CM; Department of General Surgery, Guangzhou First People's Hospital Affiliated to Guangzhou Medical University, Guangzhou, Guangdong, China.
Genet Mol Res ; 14(4): 14440-7, 2015 Nov 19.
Article em En | MEDLINE | ID: mdl-26600502
ABSTRACT
Osteopontin (OPN) plays an important role in the metastasis and recurrence of tumors after resection of hepatocellular carcinoma (HCC). In this study, the down-regulation effect on OPN expression in HCC cells of RNA interference (RNAi) molecules designed to target different segments of OPN was investigated to identify a more effective site for OPN knockdown. Specific small interfering RNAs (siRNAs A, B, and C) of OPN were synthesized and transfected into an HCC cell line (HEP-G2; representing the OPNi-A, OPNi-B, and OPNi-C groups). Fluorescent quantitative polymerase chain reaction and immunohistochemical methods were used to detect the mRNA and protein expression of OPN before and after RNAi. Results showed that after transfection, the fluorescence intensity of the OPNi-A group was greater than those of the OPNi-B and OPNi-C groups. After 48 h of transfection, the ΔCT values of OPN mRNA expression in the OPNi-A-C groups increased from 8.31 ± 1.58, 8.78 ± 1.49, and 8.25 ± 1.51 to 12.14 ± 1.43, 10.22 ± 1.97, and 10.48 ± 1.88, respectively (P < 0.05), and the OPN protein levels (immunohistochemistry scores) decreased from 6.44 ± 1.67, 5.43 ± 2.05, and 5.45 ± 2.52 to 2.84 ± 1.52, 4.43 ± 1.65, and 3.95 ± 1.43 points, respectively. These results indicated that RNAi based on different segments of the OPN gene had different down-regulatory effects on OPN expression. Synthesis of targeted siRNA aimed at specific OPN segments might have important significance for dealing with the invasiveness and metastasis of HCC cells.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Hepatocelular / Osteopontina / Neoplasias Hepáticas / Recidiva Local de Neoplasia Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Hepatocelular / Osteopontina / Neoplasias Hepáticas / Recidiva Local de Neoplasia Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article