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©The Author(s) 2025.
World J Gastrointest Oncol. Jul 15, 2025; 17(7): 107971
Published online Jul 15, 2025. doi: 10.4251/wjgo.v17.i7.107971
Published online Jul 15, 2025. doi: 10.4251/wjgo.v17.i7.107971
Figure 6 The inhibitor of β-Catenin, iCRT3, can attenuate the cellular phenotypes induced by SAC3 domain containing 1 overexpression.
aP < 0.05, cP < 0.001. A: The iCRT3 antagonizes the enhanced cell proliferation ability caused by SAC3 domain containing 1 overexpression, bar = 100 μm; B: The iCRT3 antagonizes the enhanced cell migration ability caused by SAC3 domain containing 1 overexpression, bar = 200 μm; C: Western blotting analysis of the effects of the β-Catenin antagonist iCRT3 on the expression of c-Myc, glucose transporter 1, hexokinase 2, pyruvate kinase M2 and lactate dehydrogenase A. SAC3D1: SAC3 domain containing 1; EdU: 5-ethynyl-2’-deoxyuridine; GLUT1: Glucose transporter 1; HK2: Hexokinase 2; PKM2: Pyruvate kinase M2; LDHA: Lactate dehydrogenase A.
- Citation: Lin XJ, Tang EJ, Sun B, Wang AL, Chen Y, Chen L, Xue YY, Li AJ, Liu CY. SAC3 domain containing 1 intervention in energy metabolism reprogramming assists in the progression of hepatocellular carcinoma. World J Gastrointest Oncol 2025; 17(7): 107971
- URL: https://www.wjgnet.com/1948-5204/full/v17/i7/107971.htm
- DOI: https://dx.doi.org/10.4251/wjgo.v17.i7.107971