Author Correction: Transcription factor FoxO1 regulates myoepithelial cell diversity and growth
Rino Tokumasu, Rika Yasuhara, Seya Kang, Takahiro Funatsu, Kenji Mishima

Abstract
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Taxonomy
TopicsFOXO transcription factor regulation
Correction to: Scientific Reports 10.1038/s41598-024-51619-1, published online 11 January 2024
The original version of this Article contained an error in Fig. 4B, where, as a result of an error during figure assembly, a duplicate figure had been uploaded.
Fig. 4. FoxO1 suppressed ME cell proliferation via cell cycle arrest. (A) Viability of ME^PB-FoxO1^ cells treated with and without Dox (2 µg/mL) at the indicated time-points. (B,C) Cell proliferation rates were measured by BrdU incorporation assay. BrdU positive/DAPI (%, left) with and without Dox (2 µg/mL) for 24 h (B) or with and without transfection of siRNA for FoxO1 for 48 h (C). Immunofluorescent images were showed on the right (BrdU; green, DAPI; blue). (D–F) Expression of p27(KIP1) in ME^PB-FoxO1^ cells. Cells were treated with and without Dox (2 µg/mL) (D), pretreated with and without FoxO1 inhibitor (Inh.; AS1842856, 1 μM) (E) and transfected with siRNA for FoxO1 (F) in the presence of Dox (2 µg/mL) for 48h. The expression data of p21(CIP/WAF1) were shown in Fig. S4. (G) Chromatin immunoprecipitation-quantitative real-time PCR (ChIP-qPCR) analysis of the DNA binding activity of FoxO1 in ME cells. DNA sample was prepared from ME^PB-FoxO1^ cells treated with Dox (2 µg/mL) for 72 h. The associated DNA at the promoter regions of p21^CIP/WAF1^ (− 1722 to − 1712) and p27^KIP1^ (− 1036 to − 1026), after incubation with FoxO1 antibody-conjugated protein G beads, were immunoprecipitated and analyzed by qPCR. *P < 0.05. n = 3. All data were representative of three independent experiments. (H) A schematic for FoxO1-induced cell growth inhibition. See also Supplementary Fig. S4.
The original Article has been corrected.
