Linglong Yin1,2, Youhong Liu1,2, Yuchong Peng1,2, Yongbo Peng3, Xiaohui Yu1,2, Yingxue Gao1,2, Bowen Yuan1,2, Qianling Zhu1,2, Tuoyu Cao1,2, Leye He4, Zhicheng Gong5, Lunquan Sun1,2, Xuegong Fan6, Xiong Li7,8,9. 1. Center for Molecular Medicine, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410008, Hunan, China. 2. Hunan Key Laboratory of Molecular Radiation Oncology, Xiangya Hospital, Central South University, Changsha, China. 3. State Key Laboratory of Chemo/Biosensing and Chemometrics, Hunan University, Changsha, China. 4. Research Institute for Prostate Disease, Central South University, Changsha, China. 5. Department of Pharmacy, Xiangya Hospital, Central South University, Changsha, China. 6. Hunan Key Laboratory of Viral Hepatitis, Xiangya Hospital, Central South University, Changsha, China. 7. Center for Molecular Medicine, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410008, Hunan, China. lixiongxiangya@csu.edu.cn. 8. Hunan Key Laboratory of Molecular Radiation Oncology, Xiangya Hospital, Central South University, Changsha, China. lixiongxiangya@csu.edu.cn. 9. Research Institute for Prostate Disease, Central South University, Changsha, China. lixiongxiangya@csu.edu.cn.
Correction to: J Exp Clin Cancer Res 37, 153 (2018)https://doi.org/10.1186/s13046-018-0810-7Following publication of the original article [1], the authors identified a minor error in Fig. 4; specifically:
Fig. 4
Co-administration of SAHA and veliparib enhanced PCa cell apoptosis. PCa cells LNCaP, C4–2 and PC-3 were treated with SAHA and veliparib alone or in combination at the indicated doses for 4 days (a LNCaP. b C4–2. c PC-3. d VCap, CWR22Rv1, DU145). Cells were stained with FITC-Annexin V antibody and counterstained with PI. The apoptotic cells were analyzed by flow cytometery. Representative dot plots of FITC-Annexin V/PI staining are shown. Graph shows mean apoptotic cells (Annexin-V+/PI+) ± SD. Experiments were performed in triplicate. Cell apoptosis was validated by testing the protein levels of cleaved PARP by western blotting (a-d). *p < 0.05; ** p < 0.01 (SAHA or Veliparib alone vs. co-treatment)
Fig. 4 b: Incorrect flow cytometry graphs of VEL (20uM) and SA + VEL were used; the figure has been corrected to use the correct graphsCo-administration of SAHA and veliparib enhanced PCa cell apoptosis. PCa cells LNCaP, C4–2 and PC-3 were treated with SAHA and veliparib alone or in combination at the indicated doses for 4 days (a LNCaP. b C4–2. c PC-3. d VCap, CWR22Rv1, DU145). Cells were stained with FITC-Annexin V antibody and counterstained with PI. The apoptotic cells were analyzed by flow cytometery. Representative dot plots of FITC-Annexin V/PI staining are shown. Graph shows mean apoptotic cells (Annexin-V+/PI+) ± SD. Experiments were performed in triplicate. Cell apoptosis was validated by testing the protein levels of cleaved PARP by western blotting (a-d). *p < 0.05; ** p < 0.01 (SAHA or Veliparib alone vs. co-treatment)The corrected figure is given here. The correction does not have any effect on the final conclusions of the paper.