Table 3.
Existing inhibitors targeting the phosphoinositide 3-kinase/protein kinase B/mechanistic target of rapamycin signaling pathway in triple negative breast cancer
|
Inhibitors class
|
Inhibitors name
|
Mechanism of action/inhibition
|
Ref.
|
|
| PI3K inhibitors | Pan-PI3K inhibitors | Buparlisib (BKM120) | Block hormone receptor-mediated repair through the PI3K/AKT/NF-κB/c-Myc signaling pathway as well as the PI3K/AKT/FOXM1/Exo1 signaling pathway | [102] |
| Selective PI3K inhibitors | LY294002 | Suppress the expression of PI3K, AKT, and mTOR as well as phosphorylated protein levels activation in TNBC cells while inducing alterations in multi-kinase phosphorylation | [104] | |
| Inavolisib (GDC-0077) | Inhibit PI3K signaling as well as reduce cell viability through p110α degradation | [106,107] | ||
| mTOR inhibitors | AZD8055 | Inhibit the proliferation of breast cancer cells, inhibit glycolysis and reduce glucose consumption. Inhibit MEK1/2 activated AKT, cell cycle progression and cell proliferation | [116,117] | |
| Dual PI3K/mTOR inhibitors | BEZ235 | Inhibit HIF-1alpha expression and the PI3K/mTOR signaling pathways, induce autophagy, and prolong DNA damage repair. Suppress cell proliferation, migration, and colony formation; promote the degradation of mutant p53 | [120,122] | |
| SF1126 | Suppresses tumorigenesis and angiogenesis in vivo. Induce apoptosis by inhibiting the EGFR-PI3K/AKT/mTOR pathway | [123] | ||
| GDC-0084 | Reduce the activity of PIK3CA mutant BC BMS cell lines in vitro, induce apoptosis, and inhibit the phosphorylation of AKT and p70S6 | [124] | ||
| Gedatolisib | Stimulate the response of dendritic cells, CD8+ T cells, and natural killer cells | [125] | ||
| GDC-0980 | Induce DNA damage, inhibit proliferation signaling, upregulate the expression of apoptotic markers, and suppress tumor growth | [127] | ||
| AKT inhibitors | Ipatasertib (GDC-0068) | Bind to three subtypes of AKT, thereby inhibit AKT activity, obstruct the PI3K/AKT/mTOR signaling pathway, and diminish tumor cell proliferation and survival | [134,136] | |
| MK-2206 | Inhibit Akt phosphorylation and induct DNA damage | [139] | ||
| Capivasertib (AZD5363) | Reduce stemness and re-sensitize BCSCs to chemotherapeutic agents by modulating mitochondrial fusion | [129] | ||
PI3K: Phosphoinositide 3-kinase; Akt: Protein kinase B; mTOR: Mechanistic target of rapamycin; NF-κB: Nuclear factor-kappa B; FOXM1: Forkhead box M1; TNBC: Triple negative breast cancer; HIF: Hypoxia-inducible factor; EGFR: Epidermal growth factor receptor; BCSC: Breast cancer stem cell; PIK3CA: Phosphoinositide3 kinase-alpha.