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CLC number: R735.3+5

On-line Access: 2013-06-04

Received: 2012-08-24

Revision Accepted: 2013-01-11

Crosschecked: 2013-05-25

Cited: 8

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Citations:  Bibtex RefMan EndNote GB/T7714

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Journal of Zhejiang University SCIENCE B 2013 Vol.14 No.6 P.451-459


Effect of siRNA-mediated knockdown of eIF3c gene on survival of colon cancer cells

Author(s):  Ning Song, Yan Wang, Xiao-dong Gu, Zong-you Chen, Liu-bin Shi

Affiliation(s):  Department of General Surgery, Huashan Hospital, Fudan University, Shanghai 200040, China

Corresponding email(s):   linbinshi@163.com

Key Words:  Eukaryotic initiation factor subunit c (eIF3c), Colon cancer, RKO cells, Small interfering RNA (siRNA)

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Ning Song, Yan Wang, Xiao-dong Gu, Zong-you Chen, Liu-bin Shi. Effect of siRNA-mediated knockdown of eIF3c gene on survival of colon cancer cells[J]. Journal of Zhejiang University Science B, 2013, 14(6): 451-459.

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journal="Journal of Zhejiang University Science B",
publisher="Zhejiang University Press & Springer",

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%T Effect of siRNA-mediated knockdown of eIF3c gene on survival of colon cancer cells
%A Ning Song
%A Yan Wang
%A Xiao-dong Gu
%A Zong-you Chen
%A Liu-bin Shi
%J Journal of Zhejiang University SCIENCE B
%V 14
%N 6
%P 451-459
%@ 1673-1581
%D 2013
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B1200230

T1 - Effect of siRNA-mediated knockdown of eIF3c gene on survival of colon cancer cells
A1 - Ning Song
A1 - Yan Wang
A1 - Xiao-dong Gu
A1 - Zong-you Chen
A1 - Liu-bin Shi
J0 - Journal of Zhejiang University Science B
VL - 14
IS - 6
SP - 451
EP - 459
%@ 1673-1581
Y1 - 2013
PB - Zhejiang University Press & Springer
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DOI - 10.1631/jzus.B1200230

eukaryotic initiation factor subunit c (eIF3c) has been identified as an oncogene that is over-expressed in tumor cells and, therefore, is a potential therapeutic target for gene-based cancer treatment. This study was focused on investigating the effect of small interfering RNA (siRNA)-mediated eIF3c gene knockdown on colon cancer cell survival. The eIF3c gene was observed to be highly expressed in colon cancer cell models. The expression levels of the gene in eIF3c siRNA infected and control siRNA infected cells were compared via real-time polymerase chain reaction (PCR) and western blotting analysis. Cell proliferation levels were analyzed employing 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and colony formation assays. Furthermore, the effects of eIF3c gene knockdown on the cell cycle and apoptosis were analyzed using flow cytometry. The results showed that suppression of eIF3c expression significantly (P<0.001) reduced cell proliferation and colony formation of RKO colon cancer cells. The cell cycle was arrested by decreasing the number of cells entering S phase. Further, apoptosis was induced as a result of eIF3c knockdown. Collectively, eIF3c deletion effectively reduced the survival of colon cancer cells and could be used as a therapeutic tool for colon cancer therapy.

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