PI3K/AKT/mTOR-Targeted Therapy for Breast Cancer

Phosphatidylinositol 3-kinase (PI3K), protein kinase B (PKB/AKT) and mechanistic target of rapamycin (mTOR) (PAM) pathways play important roles in breast tumorigenesis and confer worse prognosis in breast cancer patients. The inhibitors targeting three key nodes of these pathways, PI3K, AKT and mTOR...

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Main Authors: Kunrui Zhu, Yanqi Wu, Ping He, Yu Fan, Xiaorong Zhong, Hong Zheng, Ting Luo
Format: Article
Language:English
Published: MDPI AG 2022-08-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/11/16/2508
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author Kunrui Zhu
Yanqi Wu
Ping He
Yu Fan
Xiaorong Zhong
Hong Zheng
Ting Luo
author_facet Kunrui Zhu
Yanqi Wu
Ping He
Yu Fan
Xiaorong Zhong
Hong Zheng
Ting Luo
author_sort Kunrui Zhu
collection DOAJ
description Phosphatidylinositol 3-kinase (PI3K), protein kinase B (PKB/AKT) and mechanistic target of rapamycin (mTOR) (PAM) pathways play important roles in breast tumorigenesis and confer worse prognosis in breast cancer patients. The inhibitors targeting three key nodes of these pathways, PI3K, AKT and mTOR, are continuously developed. For breast cancer patients to truly benefit from PAM pathway inhibitors, it is necessary to clarify the frequency and mechanism of abnormal alterations in the PAM pathway in different breast cancer subtypes, and further explore reliable biomarkers to identify the appropriate population for precision therapy. Some PI3K and mTOR inhibitors have been approved by regulatory authorities for the treatment of specific breast cancer patient populations, and many new-generation PI3K/mTOR inhibitors and AKT isoform inhibitors have also been shown to have good prospects for cancer therapy. This review summarizes the changes in the PAM signaling pathway in different subtypes of breast cancer, and the latest research progress about the biomarkers and clinical application of PAM-targeted inhibitors.
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spelling doaj.art-06b6cc2d35ac462aa16b32767bf1bc322023-12-01T23:33:21ZengMDPI AGCells2073-44092022-08-011116250810.3390/cells11162508PI3K/AKT/mTOR-Targeted Therapy for Breast CancerKunrui Zhu0Yanqi Wu1Ping He2Yu Fan3Xiaorong Zhong4Hong Zheng5Ting Luo6Breast Disease Center, Cancer Center, West China Hospital, Sichuan University, Chengdu 610000, ChinaBreast Disease Center, Cancer Center, West China Hospital, Sichuan University, Chengdu 610000, ChinaBreast Disease Center, Cancer Center, West China Hospital, Sichuan University, Chengdu 610000, ChinaMulti-Omics Laboratory of Breast Diseases, State Key Laboratory of Biotherapy, National Collaborative, Innovation Center for Biotherapy, West China Hospital, Sichuan University, Chengdu 610000, ChinaBreast Disease Center, Cancer Center, West China Hospital, Sichuan University, Chengdu 610000, ChinaBreast Disease Center, Cancer Center, West China Hospital, Sichuan University, Chengdu 610000, ChinaBreast Disease Center, Cancer Center, West China Hospital, Sichuan University, Chengdu 610000, ChinaPhosphatidylinositol 3-kinase (PI3K), protein kinase B (PKB/AKT) and mechanistic target of rapamycin (mTOR) (PAM) pathways play important roles in breast tumorigenesis and confer worse prognosis in breast cancer patients. The inhibitors targeting three key nodes of these pathways, PI3K, AKT and mTOR, are continuously developed. For breast cancer patients to truly benefit from PAM pathway inhibitors, it is necessary to clarify the frequency and mechanism of abnormal alterations in the PAM pathway in different breast cancer subtypes, and further explore reliable biomarkers to identify the appropriate population for precision therapy. Some PI3K and mTOR inhibitors have been approved by regulatory authorities for the treatment of specific breast cancer patient populations, and many new-generation PI3K/mTOR inhibitors and AKT isoform inhibitors have also been shown to have good prospects for cancer therapy. This review summarizes the changes in the PAM signaling pathway in different subtypes of breast cancer, and the latest research progress about the biomarkers and clinical application of PAM-targeted inhibitors.https://www.mdpi.com/2073-4409/11/16/2508AKTbiomarkerbreast cancercancer therapymTORPI3K
spellingShingle Kunrui Zhu
Yanqi Wu
Ping He
Yu Fan
Xiaorong Zhong
Hong Zheng
Ting Luo
PI3K/AKT/mTOR-Targeted Therapy for Breast Cancer
Cells
AKT
biomarker
breast cancer
cancer therapy
mTOR
PI3K
title PI3K/AKT/mTOR-Targeted Therapy for Breast Cancer
title_full PI3K/AKT/mTOR-Targeted Therapy for Breast Cancer
title_fullStr PI3K/AKT/mTOR-Targeted Therapy for Breast Cancer
title_full_unstemmed PI3K/AKT/mTOR-Targeted Therapy for Breast Cancer
title_short PI3K/AKT/mTOR-Targeted Therapy for Breast Cancer
title_sort pi3k akt mtor targeted therapy for breast cancer
topic AKT
biomarker
breast cancer
cancer therapy
mTOR
PI3K
url https://www.mdpi.com/2073-4409/11/16/2508
work_keys_str_mv AT kunruizhu pi3kaktmtortargetedtherapyforbreastcancer
AT yanqiwu pi3kaktmtortargetedtherapyforbreastcancer
AT pinghe pi3kaktmtortargetedtherapyforbreastcancer
AT yufan pi3kaktmtortargetedtherapyforbreastcancer
AT xiaorongzhong pi3kaktmtortargetedtherapyforbreastcancer
AT hongzheng pi3kaktmtortargetedtherapyforbreastcancer
AT tingluo pi3kaktmtortargetedtherapyforbreastcancer