化学
PI3K/AKT/mTOR通路
mTOR抑制剂的发现与发展
背景(考古学)
蛋白激酶B
药理学
癌症
替西罗莫司
癌症研究
生物化学
生物
信号转导
内科学
医学
古生物学
作者
Maria Antonietta Occhiuzzi,Gernando Lico,Giuseppina Ioele,Michele De Luca,Antonio Garofalo,Fedora Grande
标识
DOI:10.1016/j.ejmech.2022.114971
摘要
The biochemical role of the PI3K/PKB/mTOR signalling pathway in cell-cycle regulation is now well known. During the onset and development of different forms of cancer it becomes overactive reducing apoptosis and allowing cell proliferation. Therefore, this pathway has become an important target for the treatment of various forms of malignant tumors, including breast cancer and follicular lymphoma. Recently, several more or less selective inhibitors targeting these proteins have been identified. In general, drugs that act on multiple targets within the entire pathway are more efficient than single targeting inhibitors. Multiple inhibitors exhibit high potency and limited drug resistance, resulting in promising anticancer agents. In this context, the present survey focuses on small molecule drugs capable of modulating the PI3K/PKB/mTOR signalling pathway, thus representing drugs or drug candidates to be used in the pharmacological treatment of different forms of cancer.
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