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. 2025 Apr 25;13(2):92–117. doi: 10.62347/QCPV6064

Table 2.

Autophagy-related medications for breast cancer

Drug Application Status Target Tumor or cell Type Autophagy Activity Mechanism Reference
BafA1 Research Autophagosome Breast cancer Inhibition Enhancing radiation-induced death in breast cancer cells by likely modulating endoplasmic stress and mTOR pathway [119]
Chloroquine (CQ) Clinical Application Autophagosome Breast cancer Inhibition Boosting radiation sensitivity by suppressing TAK1; improving cytotoxicity of chemotherapy in resistant tumors [119,120]
Ipatasertib Preclinical & Clinical Trials PI3K/AKT Breast cancer Induction Induces autophagy in TNBC, enhancing antitumor activity of PI3K/AKT suppressors in combination with CQ [121]
Taselisib Preclinical & Clinical Trials PI3K/AKT Breast cancer Induction Similar to Ipatasertib, inducing autophagy in TNBC, potentiating antitumor effects of chemotherapy with CQ [121]
Tamoxifen Clinical Application ER Breast cancer Induction Induces autophagy in ER+ breast cancer cells, potentially contributing to cell survival and resistance [122]
Lapatinib Clinical Application HER2/EGFR Breast cancer Dual Activity Short-term treatment induces apoptosis via autophagy; long-term treatment leads to protective autophagy [123]
Trastuzumab Clinical Application HER2 Breast cancer Not Specified Autophagy plays a significant role in the cytotoxic effects of trastuzumab and T-DM1 on HER2+ breast cancer cells [124,125]
Artemisinin Research Beclin-1, P21 MCF-7, MDA-MB-231 Up-regulation Inducing autophagy by up-regulating Beclin-1 and P21, leading to increased sensitivity to chemotherapy and apoptosis [126-129]
Baicalein Research PI3K/AKT, mTOR MCF-7, MDA-MB-231 Activation Suppressing cell proliferation and triggers apoptosis and Inducing autophagy by modulating the PI3K/AKT/mTOR pathway [130-133]
Britannin Research ATG1, ATG4, ATG5 MCF-7 Inhibition Inducing apoptosis and inhibits autophagy by down-regulating autophagy markers such as ATG4, ATG5, Beclin1, and LC-III [134,135]
Celastrol Research LC3 A/B, p62 MCF-7 Activation Exhibits antiproliferative activity and inhibits colony formation by elevating expression of autophagy markers LC3 A/B, p62, and Beclin-1 [137-139]
Cucurbitacin B Research LC3 II, p-mTOR MCF-7 Activation Decreasing cell viability and inducing DNA damage and autophagy by up-regulating LC3 II and inhibiting p-mTOR, p-Akt, and p62 expressions [140-142]
Curcumin Research PI3K/Akt/mTOR MCF7, MDA-MB-231 Activation Sensitizing MDR breast cancer cells to cisplatin and inducing apoptosis and autophagy by down-regulating CCAT1 and inactivating the PI3K/Akt/mTOR pathway [143-145]
Gaillardin Research ATG1, ATG4, ATG5 MCF-7 Inhibition Inducing apoptosis and inhibiting autophagy by down-regulating autophagy markers such as ATG1, ATG4, ATG5, Beclin1, and LC-III [136]
Icariin Research CDK2, CDK4 MCF-7, MDA-MB-231 Dual Activity Inducing cell cycle arrest and apoptosis through suppression of autophagy in TAM-resistant cells and enhances autophagy in other contexts [146-148]
Paclitaxel Research Beclin1 BT474 Inhibition Inhibiting tumor growth by reducing the expression of Beclin1 [149-151]
Resveratrol Research AKT, mTORC1 MDA-MB-231, MCF-7 Dual Activity Sensitizing breast cancer cells to talazoparib and inducing apoptosis by suppressing AKT signaling and inhibiting autophagy flux [152-154]
Tetrandrine Research PI3K/AKT/mTOR MDA-MB-231, MCF-7 Activation Blocks cell proliferation and stimulating autophagy and apoptosis by elevating Beclin1, LC3-II/LC3-I and reducing p62/SQSTM1 [155-157]
Thymoquinone Research Beclin-1, LC3 MCF-7, MDA-MB-231 Dual Activity Inhibiting autophagy and cell migration in some contexts, while in others, it increases autophagic vesicles and sensitizes cells to PTX [158-160]
Tocotrienols Research Beclin-1, LC3B MCF-7, MDA-MB-231 Activation Decreasing cancer cell viability by increasing markers of both early and late phase autophagy [161-163]
Ursolic acid Research PI3K, AKT MCF-7, MDA-MB-231 Activation Inducing cytotoxic autophagy and apoptosis by diminishing AKT signaling and affecting glycolysis [164-166]