癌症研究
转录组
癌症
细胞培养
细胞生长
细胞周期
信号转导
生物
细胞
癌细胞
小分子
癌症干细胞
细胞信号
靶向治疗
细胞凋亡
细胞周期检查点
基因表达
化学
干细胞
基因
医学
毒性
癌变
基因表达调控
下调和上调
生长抑制
遗传增强
作者
Te‐Sheng Chang,Chin Li,Wei‐Ming Chen,Yung‐Yu Hsieh,KUO-LIANG WEI,Chung‐Kuang Lu,Ming‐Ko Chiang
出处
期刊:Anticancer Research
[International Institute of Anticancer Research (IIAR) Conferences 1997. Athens, Greece. Abstracts]
日期:2026-03-27
卷期号:46 (4): 1917-1927
标识
DOI:10.21873/anticanres.18084
摘要
BACKGROUND/AIM: Gastric cancer (GC) remains a major public health concern both in Taiwan and worldwide. While advances in public health have reduced its incidence rate, clinical outcomes of advanced GC remain suboptimal with current standard therapy. The Wnt/β-catenin signaling pathway is frequently up-regulated in GC, promoting tumor progression. This study investigated the anti-tumor effects of PKF118-310, a small molecule inhibitor of the β-catenin-TCF/LEF interaction, in GC cell lines and patient-derived models. MATERIALS AND METHODS: . RESULTS: gene expression correlated with PKF118-310 sensitivity. In PDX models, PKF118-310 reduced tumor growth without affecting body weight. CONCLUSION: PKF118-310 exhibits potent anti-tumor effects in GC by inhibiting the Wnt/β-catenin signaling pathway, reducing tumor growth, and targeting CSCs. These findings suggest PKF118-310 as a promising therapeutic candidate for GC treatment.
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