PI3K/AKT/mTOR通路
自噬
蛋白激酶B
背景(考古学)
药物发现
信号转导
细胞凋亡
癌细胞
激酶
癌症
体内
化学
生物
癌症研究
药理学
细胞生物学
生物化学
生物技术
遗传学
古生物学
作者
Manuele Figueiredo da Silva,Arestides Alves Lins,Midiane Correia Gomes,Washley Phyama de Jesus Marinho,Rodrigo Santos Aquino de Araújo,Ricardo Olímpio de Moura,Peng Zhan,Igor José dos Santos Nascimento,Edeildo Ferreira da Silva Júnior
标识
DOI:10.2174/0109298673325229240928040758
摘要
The term cancer is used to describe a complex pathology characterized by the uncontrollable proliferation of cells, which displays a fast metastatic spread, being a disease with difficult treatment. In this context, Phosphatidylinositol 3-kinase (PI3K) represents a promising pathway to be inhibited, aiming to develop anticancer agents, since it performs a pivotal role in regulating essential cellular processes, including cell proliferation, growth, autophagy, and apoptosis. In parallel, natural compounds can effectively represent a therapeutic strategy to fight against malignant cells. Then, compounds derived from various plant sources, such as flavonoids, terpenoids, alkaloids, coumarins, and lignans, have exhibited remarkable in vitro and in vivo anticancer properties. This review focused in the exploration of natural products targeting the PI3K/AKT/m-TOR signaling pathway, demonstrating that these compounds could even further investigated to reveal novel and effective anticancer drugs in the future.
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