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©The Author(s) 2025.
World J Gastrointest Oncol. Jan 15, 2025; 17(1): 99376
Published online Jan 15, 2025. doi: 10.4251/wjgo.v17.i1.99376
Published online Jan 15, 2025. doi: 10.4251/wjgo.v17.i1.99376
Figure 6 Effect of BIBR1532 on shelterin protein and key proteins in the DNA damage response pathway expression in KYSE150 and KYSE410 cells.
A and B: Expression of telomeric-repeat binding factor 1 (TRF1), TRF2, TIN2-interacting protein 1, protection of telomeres 1, TIN2, and repressor activation protein 1 in KYSE150 (A) and KYSE410 (B) cells after treatment with indicated concentrations of BIBR1532 for 48 hours; C and D: Expression of γ-H2AX, p-ATM, CHK2, p-ATR, and CHK1 in KYSE150 (C) and KYSE410 (D) cells after treatment with the indicated concentrations of BIBR1532 for 48 hours. TRF1: Telomeric-repeat binding factor 1; TRF2: Telomeric-repeat binding factor 2; TPP1: TIN2-interacting protein 1; POT1: Protection of telomeres 1; TIN2: TRF1-interacting nuclear protein 2; RAP1: Repressor activation protein 1; γ-H2AX: Phosphorylated histone H2AX; p-ATM: Phosphorylated ataxia-telangiectasia mutated gene; p-ATR: Phosphorylated ataxia telangiectasia and Rad3-related protein; CHK2: Check point kinase 2; CHK1: Check point kinase 1.
- Citation: Wang Q, Li QR, Xu L, Yuan ZC, Liu X, Tang MJ, Luo M, Zhong XW, Ma Q, Guo XL. BIBR1532 inhibits proliferation and metastasis of esophageal squamous cancer cells by inducing telomere dysregulation. World J Gastrointest Oncol 2025; 17(1): 99376
- URL: https://www.wjgnet.com/1948-5204/full/v17/i1/99376.htm
- DOI: https://dx.doi.org/10.4251/wjgo.v17.i1.99376