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. 2026 Oct 13;12:73. doi: 10.1038/s41421-026-00932-2

Author Correction: Breast cancer induces CD62L+ Kupffer cells via DMBT1 to promote neutrophil extracellular trap formation and liver metastasis

Pu Tian 1, Qiuyao Wu 1, Dasa He 1, Wenjing Zhao 2, Lichao Luo 1, Zhenchang Jia 1, Wenqian Luo 1, Xianzhe Lv 1, Yanan Liu 1, Yuan Wang 1, Qian Wang 1, Peiyuan Zhang 1, Yajun Liang 1,✉, Qifeng Yang 2,✉, Guohong Hu 1,✉
PMCID: PMC13661528  PMID: 42869879

Correction to: Cell Discovery https://www.nature.com/articles/s41421-025-00819-8, published online 12 August 2025

In Fig. 6g of the initially published version of the article, the representative images of KD1 and KD2 contained partially overlapped/similar areas due to a mislabeling for the file name, and thus a KD1 (kd4 in file names) image was mislabeled as KD2 (kd5 in file names), or vice versa. In addition, the P value was mislabeled from 0.0003 to 0.003. The corrected Fig. 6 is provided below, with both mislabeled images replaced and P value corrected. The authors apologize for the negligence and any inconvenience caused by the erratum. The figure error did not affect any conclusion of the article.

Correct Fig. 6

Fig. 6. DMBT1 promotes liver metastasis of breast cancer.

Fig. 6

a–c In vivo BLI (a), ex vivo BLI (b) and NETosis (c) in livers of NOD-SCID mice treated with Clod after intrasplenic inoculation of MCF7 with or without DMBT1 overexpression. d–f In vivo BLI (d), ex vivo BLI (e) and NETosis (f) of NOD-SCID mice treated with GSK484 after intrasplenic inoculation of MCF7 with or without DMBT1 overexpression. g–j NETosis (g), CD62L+ KCs (h) and in vivo BLI (i) of livers, and survival (j) of nude mice after intrasplenic injection of LvM16 cells with DMBT1 knockdown. k, l Primary tumor growth (k) and liver metastasis (l) in C57BL/6 mice after orthotopic injection of AT3 cells with Dmbt1 knockdown. n = 3 or 4 (a, b), 3 (c, h, k, l), 7 (d, i, j), 4 (e, f, g) mice per group. P values were obtained by repeated measures two-way ANOVA (a, d, i, k), Log rank test (j) or two-tailed unpaired t-test (others). Scale bars, 50 μm. Data are shown as mean ± SEM (a, d, i, k) or mean ± SD (others).

Incorrect Fig. 6

Fig. 6. DMBT1 promotes liver metastasis of breast cancer.

Fig. 6

a–c In vivo BLI (a), ex vivo BLI (b) and NETosis (c) in livers of NOD-SCID mice treated with Clod after intrasplenic inoculation of MCF7 with or without DMBT1 overexpression. d–f In vivo BLI (d), ex vivo BLI (e) and NETosis (f) of NOD-SCID mice treated with GSK484 after intrasplenic inoculation of MCF7 with or without DMBT1 overexpression. g–j NETosis (g), CD62L+ KCs (h) and in vivo BLI (i) of livers, and survival (j) of nude mice after intrasplenic injection of LvM16 cells with DMBT1 knockdown. k, l Primary tumor growth (k) and liver metastasis (l) in C57BL/6 mice after orthotopic injection of AT3 cells with Dmbt1 knockdown. n = 3 or 4 (a, b), 3 (c, h, k, l), 7 (d, i, j), 4 (e, f, g) mice per group. P values were obtained by repeated measures two-way ANOVA (a, d, i, k), Log rank test (j) or two-tailed unpaired t-test (others). Scale bars, 50 μm. Data are shown as mean ± SEM (a, d, i, k) or mean ± SD (others).

Contributor Information

Yajun Liang, Email: yjliang@sinh.ac.cn.

Qifeng Yang, Email: qifengy_sdu@163.com.

Guohong Hu, Email: ghhu@sinh.ac.cn.


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