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. 2025 May 24;16(5):104623. doi: 10.5306/wjco.v16.i5.104623

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.