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. 2021 Sep 9;11:17946. doi: 10.1038/s41598-021-97073-1

Figure 4.

Figure 4

Fluorescence imaging and diagnostic potential of freshly resected human hepatocellular carcinoma (HCC) specimens. (a) Representative fluorescence images (case 22) obtained after spraying the specimens with 50 μM SPiDER-βGal, captured using IVIS Lumina Series III (Excitation: 520 nm, Emission: 570 nm). Scale bar = 10 mm. Guide map (white light): The areas surrounded by the red lines indicate the tumour (right). (b) Time-dependent changes in fluorescence intensities of tumour and non-tumour tissue after spraying SPiDER-βGal (50 μM) (case 22). (c) Box-and-whisker plot of time-dependent changes in fluorescence intensities of the tumour (blue) and non-tumour (green) tissues after spraying 50 μM SPiDER-βGal (HCC, n = 27). Means (cross), medians (horizontal line within box), inter-quartile ranges (box), and ranges (error bars) are indicated. The median fluorescence intensity of the tumour tissues was significantly higher than that of non-tumour tissues after 2 min of spraying SPiDER-βGal (50 μM). *p < 0.05, **p < 0.01. A two-tailed Wilcoxon t-test was used. (d) Receiver operating characteristic (ROC) curves of the increase in fluorescence intensities from 0 to 10 min. The yellow line is a 45° straight line tangent to the ROC curve. (e) ROC curves of the increase in fluorescence intensities from 0 to 30 min. The yellow line is a 45° straight line tangent to the ROC curve.