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©The Author(s) 2025.
World J Diabetes. May 15, 2025; 16(5): 102994
Published online May 15, 2025. doi: 10.4239/wjd.v16.i5.102994
Published online May 15, 2025. doi: 10.4239/wjd.v16.i5.102994
Figure 4 TERT activates FOXO1 transcription to inhibit ATG9A expression.
A: JASPAR was used to analyze the binding of FOXO1 to the ATG9A promoter; B and C: Dual-luciferase reporter gene and ChIP assays were used to verify the targeting of FOXO1 to ATG9A; D and E: Reverse transcription quantitative polymerase chain reaction and western blotting were used to analyze the expression of TERT, FOXO1 and ATG9A in cells after the cells were transfected with sh-TERT or/and sh-ATG9A. The data are expressed as mean ± SD. Each experiment was conducted in triplicate. aP < 0.05 vs sh-NC, IgG, and NC groups, bP < 0.05 vs sh-NC, IgG, and NC groups, cP < 0.05 vs sh-TERT + sh-NC group. HG: High glucose.
- Citation: Lei XT, Chen XF, Qiu S, Tang JY, Geng S, Yang GY, Wu QN. TERT/FOXO1 signaling promotes islet β-cell dysfunction in type 2 diabetes mellitus by regulating ATG9A-mediated autophagy. World J Diabetes 2025; 16(5): 102994
- URL: https://www.wjgnet.com/1948-9358/full/v16/i5/102994.htm
- DOI: https://dx.doi.org/10.4239/wjd.v16.i5.102994