TY - JOUR
T1 - Erratum
T2 - PBN11-8, a cytotoxic polypeptide purified from marine bacillus, suppresses invasion and migration of human hepatocellular carcinoma cells by targeting focal adhesion kinase pathways (Polymers 2018, 10, 1043)
AU - Zheng, Lanhong
AU - Zhu, Xiangjie
AU - Yang, Kangli
AU - Zhu, Meihong
AU - Farooqi, Ammad Ahmad
AU - Kang, Daole
AU - Sun, Mi
AU - Xu, Yixin
AU - Lin, Xiukun
AU - Feng, Yingang
AU - Liang, Fangfang
AU - Zhang, Fuming
AU - Linhardt, Robert J.
N1 - Publisher Copyright:
© 2021, MDPI AG. All rights reserved.
PY - 2021/1
Y1 - 2021/1
N2 - The authorswish tomake a change to the published paper [1]. In the originalmanuscript, the subfigures (0 h and 12 h) were repeated by mistake in Figure 1d. The corrected Figure 1 is presented below: (Figure Presented). Figure 1. PBN11-8 displays potent cytotoxicity to cancer cells. (a) Cells were treated with certain concentrations of PBN11-8. The cell inhibitory rate was determined by MTT assay as described in the experimental section. The IC50 values were 1.56, 1.80, 1.57 and 1.73 g/mL for BEL-7402, 786-0, HepG2 and Panc-28 cells, respectively. The IC50 values were 11.79 and 14.72 g/mL for HK2 and L02 cells, respectively. (b) Cells were cultured in a 96-well plate and treated with 4 g/mL PBN11-8 for each cell line for 0, 12, 24, and 48 h to study the time dependent analysis. Cell viability was analyzed by MTT assay. (c) The results of the crystal violet adhesion assay in BEL-7402 cells induced by 1, 2, 4 g/mL of PBN11-8 for 12 h. (d) The results of the crystal violet adhesion assay in BEL-7402 cells induced by 2 g/mL of PBN11-8 for 12, 24 and 48 h. (e,f) The quantitative evaluations of the crystal violet adhesion assay. The data represent the mean SD of three independent experiments. * p < 0.05 vs. control; and ** p < 0.01 vs. control. The authors apologize for any inconvenience caused and the change does not affect the scientific results. The manuscript will be updated, and the original will remain online on the article webpage at https://www.mdpi.com/2073-4360/10/9/1043.
AB - The authorswish tomake a change to the published paper [1]. In the originalmanuscript, the subfigures (0 h and 12 h) were repeated by mistake in Figure 1d. The corrected Figure 1 is presented below: (Figure Presented). Figure 1. PBN11-8 displays potent cytotoxicity to cancer cells. (a) Cells were treated with certain concentrations of PBN11-8. The cell inhibitory rate was determined by MTT assay as described in the experimental section. The IC50 values were 1.56, 1.80, 1.57 and 1.73 g/mL for BEL-7402, 786-0, HepG2 and Panc-28 cells, respectively. The IC50 values were 11.79 and 14.72 g/mL for HK2 and L02 cells, respectively. (b) Cells were cultured in a 96-well plate and treated with 4 g/mL PBN11-8 for each cell line for 0, 12, 24, and 48 h to study the time dependent analysis. Cell viability was analyzed by MTT assay. (c) The results of the crystal violet adhesion assay in BEL-7402 cells induced by 1, 2, 4 g/mL of PBN11-8 for 12 h. (d) The results of the crystal violet adhesion assay in BEL-7402 cells induced by 2 g/mL of PBN11-8 for 12, 24 and 48 h. (e,f) The quantitative evaluations of the crystal violet adhesion assay. The data represent the mean SD of three independent experiments. * p < 0.05 vs. control; and ** p < 0.01 vs. control. The authors apologize for any inconvenience caused and the change does not affect the scientific results. The manuscript will be updated, and the original will remain online on the article webpage at https://www.mdpi.com/2073-4360/10/9/1043.
UR - https://www.scopus.com/pages/publications/85099298192
U2 - 10.3390/polym13010166
DO - 10.3390/polym13010166
M3 - Comment/debate
AN - SCOPUS:85099298192
SN - 2073-4360
VL - 13
SP - 1
EP - 2
JO - Polymers
JF - Polymers
IS - 1
M1 - 166
ER -