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. 2013 Jul 1;13:323. doi: 10.1186/1471-2407-13-323

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Copyright © 2013 Pan et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Jab1 knockdown enhanced the effects of T83 on cell viability inhibition and apoptosis induction. CNE2 cells (left) and CNE2R cells (right) were transfected with control siRNA (Cont-si) or Jab1 siRNA (Jab1-si) and then exposed to the indicated doses of T83 for 48 h; they were then examined for colony formation (A), sub-G1 (B), and cleaved caspase-3 (C-Caspase 3) (C). Protein levels were quantified with use of ImageJ software. All data represent three independent experiments, mean ± s.d. DMSO was used as control in “0” groups.