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. 2025 Jun 15;15(14):7176–7177. doi: 10.7150/thno.118171

Melatonin enhances sorafenib-induced cytotoxicity in FLT3-ITD acute myeloid leukemia cells by redox modification: Erratum

Tian Tian 1,*, Jiajun Li 1,*, Yizhuo Li 1,*, Yun-Xin Lu 1,*, Yan-Lai Tang 3, Hua Wang 1, Fufu Zheng 3, Dingbo Shi 1, Qian Long 1, Miao Chen 1, Guillermo Garcia-Manero 4, Yumin Hu 1,, Lijun Qin 2,, Wuguo Deng 1,
PMCID: PMC12204075  PMID: 40585974

The authors regret some incorrect flow cytometry scatter diagrams were accidentally displayed during data organization in Figure 1C, Figure 2F and Figure 3F. The authors confirm that these corrections do not change the result interpretation or conclusions of the article. The authors apologize for any inconvenience that the errors may have caused.

Figure 1.

Figure 1

(C) Representative images of cell apoptosis in the indicated cells treated with melatonin for 48 h were determined by Annexin-V/propidium iodide (PI) assay (red numbers indicate subpopulation of cells negative for Annexin V/PI).

Figure 2.

Figure 2

(F) Reversion of Melatonin-induced cell death by the antioxidant NAC (N-acetyl-L-cysteine). BaF3/ITD and MV4-11 cells were treated with melatonin (2 mM) alone or a combination NAC (4 mM) for 48 h, then determined by Annexin-V/propidium iodide (PI) assay (red numbers indicate subpopulation of cells negative for Annexin V/PI).

Figure 3.

Figure 3

(F) Representative images of cell apoptosis in the indicated cells treated with melatonin, sorafenib or combination for 48 h (red numbers indicate subpopulation of cells negative for Annexin V/PI).


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