PI3K/AKT/mTOR通路
自噬
蛋白激酶B
结直肠癌
体内
癌症研究
小RNA
药理学
癌症
生物
医学
细胞凋亡
信号转导
细胞生物学
生物化学
内科学
基因
生物技术
作者
Yang Bai,Yao Xiong,Yuanyuan Zhang,Lin Cheng,Hui Liu,Ke Xu,Yi‐Ying Wu,Jeffrey Field,Xiaodong Wang,Liming Zhou
标识
DOI:10.1142/s0192415x22500719
摘要
Combining innocuous natural products with cytotoxic agents may enhance the effectiveness of chemotherapy. Tangeretin is a citrus flavonoid that has antineoplastic properties, but its mechanism of action is still unknown. Here, we used a high throughput-screening (HTS) platform to screen for drugs that may synergize with tangeretin and confirmed the top hits against colorectal cancer (CRC) cells in vitro and in vivo. 5-Fluorouracil (5-FU) and PI3K/Akt inhibitors have come out as top hits that show a strong synergy effect with tangeretin by HTS. We further confirmed the synergistic effect of tangeretin with 5-FU against CRC cells in vitro and in vivo. Since 5-FU can increase microRNA-21 (miR-21) expression and activate PI3K/Akt signaling, we addressed if tangeretin acted at this level. In 5-FU treated cells, tangeretin inhibited miR-21 induction, rescued the expression of the target PTEN, reduced Akt activation, and induced autophagy. Together, our data indicated that a natural product, such as tangeretin, can modulate miR-21 expression and that this pathway might be a potential therapeutic target for CRC. Combining tangeretin with 5-FU may be useful in the clinic, since 5-FU is the current first line drug for treating CRC.
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