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. 2021 Jul 6;46(2):180. doi: 10.3892/or.2021.8131

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Copyright: © Wen 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. — Expression levels of RORβ in GC cells. (A) RORβ expression levels in GC cells were analyzed using western blotting. (B) Overexpression of RORβ in AGS cells was examined using western blotting. (C) AGS cells were subjected to nuclear/cytosolic fractionation, and RORβ expression levels were analyzed using western blotting. (D) RORβ expression levels in GC tissues were analyzed using immunohistochemical staining. (E) mRNA expression levels of RORβ were analyzed in GC tissues using reverse transcription-quantitative PCR. Data were analyzed using a Student's t-test. *P<0.05 and **P<0.01. RORβ, retinoic acid-related orphan receptor β; GC, gastric cancer; ov-, overexpression.