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. 2024 Feb 5;15:104–105. doi: 10.18632/oncotarget.28536

Correction: Targeting programmed cell death ligand 1 by CRISPR/Cas9 in osteosarcoma cells

Yunfei Liao 1,2, Lulu Chen 1, Yong Feng 2,3, Jacson Shen 2, Yan Gao 2, Gregory Cote 4, Edwin Choy 4, David Harmon 4, Henry Mankin 2, Francis Hornicek 2, Zhenfeng Duan 2,
PMCID: PMC10852055  PMID: 38329729

This article has been corrected: In Figure 1B, the β-actin panel is an accidental duplicate of the β-actin panel in Figure 2D. The corrected Figure 1, produced using the original data, is shown below. The authors declare that these corrections do not change the results or conclusions of this paper.

Figure 1. Expression of PD-L1 protein in osteosarcoma cell lines and osteosarcoma patient tissues.

Figure 1

(A) Representative images of different immunohistochemical staining intensities of PD-L1 are shown in osteosarcoma tissues. The percentage of cells showing positive cytoplasmic staining for PD-L1 was calculated by reviewing the entire spot. Based on the PD-L1 staining intensities in the tumor samples, the staining patterns were categorized into 4 groups: no staining (0), weak staining (1+), moderate staining (2+) and intense staining (3+) (Original magnification, 400×). (B) Expression of PD-L1 protein in osteosarcoma cell lines and normal osteoblast cell lines. (C) Kaplan-Meier overall survival curve of patients with osteosarcoma were subgrouped as either PD-L1 low staining (staining ≤ 1) or high staining (staining ≥ 2). (D) Kaplan-Meier five-year survival curve of patients with osteosarcoma were subgrouped as either PD-L1 low staining (staining ≤ 1) or high staining (staining ≥ 2).

Original article: Oncotarget. 2017; 8:30276–30287. 30276-30287. https://doi.org/10.18632/oncotarget.16326


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