Targeting the PI3K Pathway: Advancements and Achievements in Breast Cancer Therapy

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
出处
期刊:Current Pharmaceutical Design [Bentham Science Publishers]
卷期号:31 (31): 2481-2503 被引量:9
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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