Copyright
©The Author(s) 2015.
World J Gastroenterol. Jan 21, 2015; 21(3): 868-877
Published online Jan 21, 2015. doi: 10.3748/wjg.v21.i3.868
Published online Jan 21, 2015. doi: 10.3748/wjg.v21.i3.868
Figure 4 Suppression of tumor growth by lentivirus-mediated NOB1-siRNA in RKO cell xenograft mouse model.
A: RKO cell xenograft mice were injected intratumorally with lentivirus-mediated NOB1-siRNA, scr-siRNA, or PBS. The size of the primary tumors was measured every week. Mice were sacrificed after 5 wk. NOB1-siRNA reduced NOB-1 expression in xenografted tumor tissue as determined by Western blot; B: NOB1-siRNA induced significant apoptosis in xenografted tumor tissue detected by TUNEL staining as shown in representative images; C: Plotted percentages of apoptotic cells; D: Typical pictures from RKO cell xenografted tumors infected by PBS, src-RNA and NOB1-siRNA; E: Plotted tumor weight; F: Tumor volume in RKO cell xenograft mouse model after NOB1-siRNA infection. aP < 0.05 vs scr-siRNA. scr-siRNA: Cells infected with lentivirus-mediated scramble small interfering RNA; NOB1-siRNA: Cells infected with lentivirus-mediated NOB1-siRNA; PBS: Phosphate buffered saline.
- Citation: He XW, Feng T, Yin QL, Jian YW, Liu T. NOB1 is essential for the survival of RKO colorectal cancer cells. World J Gastroenterol 2015; 21(3): 868-877
- URL: https://www.wjgnet.com/1007-9327/full/v21/i3/868.htm
- DOI: https://dx.doi.org/10.3748/wjg.v21.i3.868