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Effects of interfering chemotactic factor Fractalkine RNA expression on biological functions of human pancreatic cancer cell lines / 中华消化杂志
Chinese Journal of Digestion ; (12): 602-606, 2012.
Article in Chinese | WPRIM | ID: wpr-420161
ABSTRACT
Objective To explore the effects of Fractalkine (FKN) on the biological functions of human pancreatic cancer cell lines SW-1990 and PNAC-1.Methods Adenovirus mediated FKN-small interfering RNA (siRNA) was transfected into human pancreatic cancer cell lines SW 1990 and PNAC-1.The differences in proliferation and invasion ability between before and after FKN-siRNA transfection were determined by clone formation assay,MTT assay and cells invasion assay.After FKN-siRNA transfection,the expression of FKN,tumor necrosis factor (TNF)-α and interleukin (IL)-6 at protein and mRNA level in human pancreatic cancer cell were detected by Western blot and reverse transcription-polymerase chain reaction (RT-PCR).The data were analyzed by one way analysis of variance.Results After human pancreatic cancer cell lines SW-1990 and PNAC-1 transfected with FKN-siRNA,the clone numbers (5.27 % ± 0.35 % and 4.60 % ± 0.30% ) increased compared with those of control group ( 1.97% ±0.25% and 1.77% ± 0.25% ) and negative FKN-siRNA group (2.10%±0.30% and 1.97%±0.25%),and the difference was statistically significant (F=113.51,103.86; both P<0.05).The clone size was also enlarged.After human pancreatic cancer cell lines SW-1990 and PNAC-1 transfected with FKN-siRNA for 48 hours and 72 hours,the MTT test results showed the absorbance value (48 h1.28±0.07 and 1.19±0.14; 72 h1.49±0.11 and 1.52±0.16) was higher than that of control group (48 h0.80±0.03 and 0.74±0.11;72 h0.89±0.03 and 0.93±0.04) and negative FKN-siRNA group (48 h0.85±0.02 and 0.76±0.05; 72 h0.89±0.02 and 1.07±0.09),and the difference was statistically significant (F=83.80,71.99,17.19,23.51; all P<0.05).The invasion ability assay showed that the invasion ability of FKN-siRNA transfected cells was stronger than that of control group and negative FKN-siRNA group,and the difference was statistically significant (F=37.37,9.08; both P<0.05).After FKN-siRNA transfection,the expression of FKN at protein and mRNA level in SW-1990 and PNAC-1 cell line decreased (proteinF=118.93 and 88.62,mRNAF=47.91 and 72.59),at the same time the expression of TNF-α and IL-6 at protein and mRNA level increased (proteinFTNF-α =112.90 and 77.88,FIL-6 =165.27 and 286.49,mRNAFTNF-α ==47.93 and 45.19,FIL-6 =36.41 and 23.67),and the differences were statistically significant (all P values<0.05).Conclusion With siRNA technology to silent FKN function,the proliferation and invasion ability of pancreatic cancer cell lines increased,which indicated FKN might inhibit certain biological functions of pancreatic cancer cells.

Full text: Available Index: WPRIM (Western Pacific) Language: Chinese Journal: Chinese Journal of Digestion Year: 2012 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Language: Chinese Journal: Chinese Journal of Digestion Year: 2012 Type: Article