Post Graduate & Research Department of Zoology, St. Joseph's College (Autonomous), Devagiri, Calicut, Kerala, 673008, India.
Curr Drug Targets. 2019;20(12):1217-1226. doi: 10.2174/1389450120666190618123846.
Phosphoinositide 3-kinase (PI3Ks) is a member of intracellular lipid kinases and involved in the regulation of cellular proliferation, differentiation and survival. Overexpression of the PI3K/Akt/mTOR signalling has been reported in various forms of cancers, especially in colorectal cancers (CRC). Due to their significant roles in the initiation and progression events of colorectal cancer, they are recognized as a striking therapeutic target.
The present review is aimed to provide a detailed outline on the role of PI3K/Akt/mTOR pathway in the initiation and progression events of colorectal cancers as well as its function in drug resistance. Further, the role of PI3K/Akt/mTOR inhibitors alone and in combination with other chemotherapeutic drugs, in alleviating colorectal cancer is also discussed. The review contains preclinical and clinical evidence as well as patent literature of the pathway inhibitors which are natural and synthetic in origin.
The data were obtained from PubMed/Medline databases, Scopus and Google patent literature.
PI3K/Akt/mTOR signalling is an important event in colorectal carcinogenesis. In addition, it plays significant roles in acquiring drug resistance as well as metastatic initiation events of CRCs. Several small molecules of natural and synthetic origin have been found to be potent inhibitors of CRCs by effectively downregulating the pathway. Data from various clinical studies also support these pathway inhibitors and several among them are patented.
Inhibitors of the PI3K/mTOR pathway have been successful for the treatment of primary and metastatic colorectal cancers, rendering the pathway as a promising clinical cancer therapeutic target.
磷酸肌醇 3-激酶(PI3Ks)是细胞内脂质激酶家族的成员,参与细胞增殖、分化和存活的调节。PI3K/Akt/mTOR 信号通路的过度表达已在各种形式的癌症中被报道,尤其是在结直肠癌(CRC)中。由于它们在结直肠癌的起始和进展事件中具有重要作用,因此被认为是一个显著的治疗靶点。
本综述旨在详细阐述 PI3K/Akt/mTOR 通路在结直肠癌起始和进展事件中的作用及其在耐药性中的功能。此外,还讨论了 PI3K/Akt/mTOR 抑制剂单独使用以及与其他化疗药物联合使用在缓解结直肠癌方面的作用。该综述包含了来自原始研究、临床试验和专利文献的有关天然和合成来源的通路抑制剂的临床前和临床证据。
数据来自 PubMed/Medline 数据库、Scopus 和 Google 专利文献。
PI3K/Akt/mTOR 信号通路是结直肠癌发生的重要事件。此外,它在获得耐药性以及 CRC 转移起始事件中也发挥着重要作用。已经发现几种天然和合成的小分子能够通过有效地下调该通路来抑制 CRC。来自各种临床研究的数据也支持这些通路抑制剂,其中一些已获得专利。
PI3K/mTOR 通路抑制剂已成功用于治疗原发性和转移性结直肠癌,使该通路成为有前途的临床癌症治疗靶点。