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] |