Your browser doesn't support javascript.
loading
[Inhibitory effect of RNA interference targeting GFI-1 on the proliferation of atypical chronic myelogenous leukemia NT1 cells].
Yang, X; Liu, H; Lin, Z H; Qian, J; Xu, X R.
Afiliação
  • Yang X; Department of Hematology, the Affiliated Hospital of Nantong University, Nantong 226000, China.
  • Liu H; Department of Hematology, the Affiliated Hospital of Nantong University, Nantong 226000, China.
  • Lin ZH; Department of Hematology, the Affiliated Hospital of Nantong University, Nantong 226000, China.
  • Qian J; Department of Hematology, the Affiliated Hospital of Nantong University, Nantong 226000, China.
  • Xu XR; School of Public Health, Nantong University, Nantong 226000, China.
Zhonghua Zhong Liu Za Zhi ; 38(8): 572-7, 2016 Aug.
Article em Zh | MEDLINE | ID: mdl-27531476
ABSTRACT

OBJECTIVE:

To investigate the inhibitory effects of RNA interference targeting GFI-1 on growth and proliferation of atypical chronic myelogenous leukemia (aCML) NT1 cells.

METHODS:

NT1 cells were transfected with PBS and liposome complex (vehicle group), scrambled siRNA and liposome complex (negative control, NC group), and GFI-1 siRNA and liposome complex (GFI-1 siRNA group), respectively. Real-time quantitative RT-PCR (qRT-PCR) and Western blot were performed to examine the expression levels of GFI-1 mRNA and protein, respectively. The proliferation abilities of NT1 cells of the three groups were evaluated by MTT assay. The cell cycle in cells of the three groups was analyzed by flow cytometry. Moreover, nude mouse xenograft model was used to detect the tumor formation ability in the three group cells.

RESULTS:

Quantitative real-time PCR data showed that the expression level of GFI-1 mRNA in GFI-1 siRNA group was significantly lower than those of NC group and vehicle group [(0.367±0.017) vs. (0.918±0.006) and (1.010±0.005), respectively, (P<0.05)]. Western blot results showed that the GFI-1 protein expression level in the GFI-1 siRNA group was also significantly reduced, compared with those of the NC group and vehicle group (P<0.05 for both). From MTT assay data, the absorbance value of NT1 cells in the GFI-1 siRNA group (0.667±0.059) was significantly lower than those of the NC group (1.096±0.049) and vehicle group (1.193±0.064, P=0.023). Flow cytometry data showed that sub-G1 and G0/G1 phase proportions of the GFI-1 siRNA group were significantly higher than those of the NC and vehicle groups [sub-G1 (8.2±2.5)% vs. (1.9±1.3)% and (2.0±3.6)%, respectively, (P<0.05); G0/G1 (66.7±3.8)% vs. (53.3±4.5)% and (48.6±3.2)%, respectively, (P<0.05)]. Furthermore, the tumor weight in the GFI-1 siRNA group [(0.37±0.02) g] was significantly lower than those in the NC group [(0.83±0.06) g] and vehicle group [(0.92±0.04) g] (P<0.05).

CONCLUSIONS:

RNA interference targeting GFI-1 inhibits the growth and proliferation of NT1 cells, which may provide a new therapeutic target for atypical chronic myelogenous leukemia.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proliferação de Células Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: Zh Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proliferação de Células Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: Zh Ano de publicação: 2016 Tipo de documento: Article