PI3K/AKT/mTOR通路
乳腺癌
临床试验
医学
蛋白激酶B
癌症研究
癌症
转移
磷酸肌醇3激酶
靶向治疗
药理学
生物信息学
信号转导
内科学
生物
细胞生物学
作者
Basavana Gowda Hosur Dinesh,Sunil Kumar Bandral,Nandini Markuli Sadashivappa,Srinivas Ganjipete,Damodar Nayak Ammunje,Selvaraj Kunjiappan,Panneerselvam Theivendren,Judy Jays,Parasuraman Pavadai
标识
DOI:10.2174/0113816128357976250122042633
摘要
Breast cancer is a complex disease caused by the aberrant and unchecked proliferation of breast cells, which leads to the development of tumours. In various types of cancer, the Phosphoinositide 3- kinase/Protein kinase B (PKB, also known as Akt (PI3K/Akt) signalling pathway, is essential for controlling cell survival, metastasis, and metabolism. Currently, marketed PI3K inhibitors for treating breast cancer face several issues, including toxicity, resistance, etc. Significant efforts have been made to develop synthetic and repurposed inhibitor drugs to target PI3K, which are now being tested in clinical trials. Developed synthetic PI3K inhibitors have been reported to have better results in clinical trials in the suppression of tumors. This review article mainly focuses on the PI3K pathway at the cellular and molecular level, the development of PI3K inhibitors, and their clinical trials. Biomarkers, marine drugs, synthetic drugs, and repurposed drugs to treat breast cancer are also discussed, followed by mutational changes in PI3K and the resistance mechanism involved in PI3K inhibitors.
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