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. 2018 Mar 22;37(26):3485–3500. doi: 10.1038/s41388-018-0161-z

Fig. 3.

Fig. 3

CREPT promoted colon cancer cell growth and tumor metastasis. a Expression levels of CREPT were increased after transfection with CREPT plasmids in colon cancer cell lines DLD-1 and HCT116 by RT-PCR and western blotting. b Knockdown efficiency of CREPT in HT29 and SW480 cell was confirmed by RT-PCR and western blotting. c Ectopic expression of CREPT significantly enhanced cell viability in both cell lines by MTT assay. d The number of colonies increased when transfected with CREPT plasmids in DLD-1 and HCT116. e Knockdown of CREPT significantly inhibited cell viability in HT29 and SW480 cell lines. f The number of colonies dramatically reduced after knockdown of CREPT in HT29 and SW480 cell lines. g Ectopic expression of CREPT significantly promoted cell viability in HCEC 1CT and 2CT cells. h CREPT overexpression accelerated HCT116 cells colony formation in soft agar. i Ectopic expression of CREPT in HCT116 cells promoted tumor growth and tumor weight in xenograft model. j Knockdown of CREPT in SW480 cells repressed tumor growth and tumor weight. IHC staining showed CREPT expression in xenograft tumor. n = 5. *P < 0.05, **P < 0.01