- Academic Editor
†These authors contributed equally.
The authors wish to make the following corrections to this paper [
1. In the Materials and Methods, Cell Growth Assay section, ‘OD values were determined after 24, 48, 72, and 96 hours to evaluate cell growth’ should instead read ‘OD values were determined after 12, 24, 36, and 48 hours to evaluate cell growth’. And ‘absorbance at 490 nm was obtained by a microplate reader’ should instead read ‘absorbance at 450 nm was obtained by a microplate reader’.
2. We have deleted an input error in Fig. 4A and have replaced it.
3. In Fig 5, in which the images of 0 h in the IOSE80 si-TMEM98 group in Fig. 5C, 6 h in the SKOV3 oe-TMEM98 group, and 12 h in the SKOV3 NC group in Fig. 5E were misused and have been replaced.
4. In Fig 12, we have deleted an input error in Fig. 12 and have replaced it.
The authors confirm that the mistakes do not affect the results and conclusions of the study and apologize for any inconvenience caused by this mistake.
(A) Compared with the NC group, the cell viability of SKOV3 cells in the
si-TMEM98 group increased significantly. (B) Compared with the NC group, the cell
viability of IOSE80 cells in the si-TMEM98 group increased significantly. (C)
Compared with the NC group, the cell viability of SKOV3 cells in the oe-TMEM98
group decreased significantly. (D) Compared with the NC group, the cell viability
of SKOV3 cells in the oe-TMEM98 group decreased significantly (n = 3, *p
Error Fig. 5.
(A,E) Test the migration ability of SKOV3 cells by scratch test. (B,F)
Quantitative analysis of the migration rate of SKOV3 cells. (C,G) Test the
migration ability of IOSE80 cells by scratch test. (D,H) Quantitative analysis
of migration rate of IOSE80 cells (n = 3, *p
Error Fig. 12.
Publisher’s Note: IMR Press stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.