PI3K/AKT/mTOR通路
自噬
蛋白激酶B
信号转导
化学
细胞生物学
生物
细胞凋亡
生物化学
作者
Z. Y. Li,Haoxian Ke,Jiawei Cai,Shubiao Ye,Junfeng Huang,Chi Zhang,Ming Yuan,Ping Lan,Xianrui Wu
摘要
ABSTRACT Objectives Methylenetetrahydrofolate dehydrogenase 1 (MTHFD1) is the enzyme with the activities of methylenetetrahydrofolate dehydrogenase, methylenetetrahydrofolate cyclohydrolase, and formyltetrahydrofolate synthetase. Our aim was to elucidate the function of MTHFD1 in colorectal cancer (CRC). Methods In vitro assessments of the proliferation, invasion, and migration abilities of CRC cells were conducted using Immunohistochemistry, Transwell invasion assays, Western blot (WB), and Cell counting Kit‐8 assays. WB was also utilized to measure autophagy protein levels and PI3K‐AKT‐mTOR signaling pathway expression. Furthermore, the role of MTHFD1 was evaluated in vivo by using subcutaneous xenograft tumor models and lateral tail vein metastasis models of human CRC in nude mice. Results Overexpression of MTHFD1 promoted the abilities of tumorigenesis and metastasis in CRC in vitro and in vivo and reduced autophagy, attributing to the PI3K‐AKT‐mTOR signaling pathway in CRC cells. In contrast, the down‐regulation of MTHFD1 increased autophagy and suppressed their proliferation, migration, and invasion. Conclusions MTHFD1 can modulate the PI3K‐AKT‐mTOR signaling pathway to suppress autophagy and stimulate tumorigenesis and metastasis.
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