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International Journal of Biological Sciences logoLink to International Journal of Biological Sciences
. 2025 Dec 15;21(15):7120–7122. doi: 10.7150/ijbs.128368

Hypoxia-activated selectivity-improved anti-PKM2 antibody combined with prodrug TH-302 for potentiated targeting therapy in hepatocellular carcinoma: Erratum

Bo Wang 1,, Fang-Zheng Qi 1,, Ping Chen 2,, Luo-Meng Qian 1, Hui-Shan Su 1, Yang Wang 1, Chen-Hui Wang 1, Ya-Xin Hou 1, Qing Zhang 2, Ding Li 2, Zhe-Sheng Chen 3, Si-He Zhang 1,
PMCID: PMC12757134  PMID: 41487912

In the process of checking the raw data, the authors noticed several inadvertent mistakes occurring in Figure 6E and Figure 7I&7J. During the preparation of these panels, the representative images showing results of H&E staining assays (Figure 6E and Figure 7I), and TUNEL staining assays (Figure 7J) were pasted and placed by mistake. The correct result should be as shown below. The authors apologize for these oversights and declare that this correction does not affect the description, interpretation, or conclusions detailed in the original paper.

FIGURE 6.

FIGURE 6

Ex vivo identification of the targeting-associated toxicity of HAP103 Ab. (E) Representative H&E staining of main organs and liver cancer tissues from mice subjected to different treatments.

FIGURE 7.

FIGURE 7

Hypoxia-targeting therapy for liver cancer via the combination of selectivity-improved HAP103 Ab and the prodrug TH-302. (I) Representative H&E staining of main organ tissues from mice subjected to different treatments. (J) Representative TUNEL staining demonstrating the degree of apoptosis in main organs and xenografted HCC tissues after different treatments. Scale bar=500 µm.


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