Correction to: J Exp Clin Cancer Res 40, 149 (2021)

https://doi.org/10.1186/s13046-021-01932-8

Following publication of the original article [1], the authors identified minor errors in Fig. 5, specifically:

  • Fig. 5h: Incorrect sphere formation image used for ALG3+LY2109761 (4th column, 1st and 2nd rows)

  • Fig. 5i: The percentage of CD44+/CD24- in the image of flow cytometry was placed in the wrong quadrant

The corrected figure is given here. The corrections do not have any effect on the final conclusions of the paper. The original article has been corrected.

Fig. 5
figure 1

ALG3 enhances radioresistance via regulation of TGFBR2 glycosylation. a Downshift of TGFBR2 bands in ALG3-sg cells was detected by Western blot. But not TGFBR1 bands (b) Representative immunofluorescence images of TGFBR2 expression level in cytoplasmic and membrane fractions. c A schematic model of different subtypes of N-glycans. The round spots are mannose, the square ones are acetylglucosamine, and the red spot is the initial of the N-glycosylation site, which is initiated by ALG3. d TGFBR2 band shift could be seen in ALG3-sg cells or cells treated by tunicamycin. And downregulation of ALG3 reduced the expression level of p-SMAD2. e Representative immunofluorescence images of p-SMAD2 expression level in cytoplasmic and nuclear fractions. Nuclear translocation of p-SMAD2 was significantly decreased in ALG3-sg and tunicamycin treatment groups. f The co-immunoprecipitation between TGFBR1 and TGFBR2, TGFBR1 and p-SMAD2 could be detected in ALG3-control group, but not tunicamycin treatment, and ALG3-sg groups. g TGFBR2 inhibitor (LY2109761) in ALG3-transduced cells decreased the surviving fraction of breast cancer cells after radiation treatment, which were detected by CCK-8 assays. Data were analyzed by two-way ANOVA. Each bar represents the mean ± SD of three independent experiments. h Inhibition of TGFBR2 in ALG3-transduced cells decreased the number of colonies after radiation treatment. i Inhibition of TGFBR2 in ALG3-transduced cells decreased the proportion of CD44+CD24 cells, which were detected by flow cytometry. “ns” no significance, *P < 0.05