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. 2017 Dec 21;15(3):3024–3030. doi: 10.3892/ol.2017.7688

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Copyright: © Wang et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 1. — Overexpression of FXYD3 in HCC. (A) Relative expression levels of FXYD3 were detected by reverse transcription-quantitative polymerase chain reaction in 80 pairs of HCC and non-cancerous normal liver tissue. In the scatterplot, each dot represents one tissue sample. The expression of FXYD3 was significantly higher in HCC compared with the non-cancerous liver tissue. (B) At the protein level, 5 pairs of samples (20.8%) showed significant expression upon western blotting. This image is representative of 3 replicates. (C) Quantification revealed that the expression of FXYD3 was significantly higher in HCC than in non-cancerous tissue. ***P<0.001 vs. normal. HCC, hepatocellular carcinoma; T, HCC; N, non-cancerous liver tissue; FYXD3, FXYD domain-containing ion transport regulator 3.