Class of Drug | Name of drug | Structure | Type of cancer to be used | Mechanism | Refs. |
---|---|---|---|---|---|
Antibiotics | Sulfisoxazole | Breast cancer | Interfering with endothelin receptor A to stop breast cancer cells from exuding tiny extracellular vesicles | [154] | |
Azithromycin | Colon cancer | ↑TNF-α-related apoptosis ↑TRAIL ↑DR4/5 ↓Autophagy | [155] | ||
Doxycycline | Osteosarcoma, prostate carcinoma, myeloid and colon cancer | In myeloid and colon cancer, it prevents permeation by lowering MMP-2 and MMP-9 | [166] | ||
Anthracycline | Endometrial, breast, bladder, hepatic, thyroid, and pulmonary malignancies | Attaches to DNA, causing it to get alkylated, which stops the cell cycle | [182] | ||
Antifungals | Itraconazole | Non-small cell lung cancer | By eliminating lipids from the plasma membrane, it decreases AKT1 activity, which inhibits its downstream target mTOR, resulting in mortality and growth slowering | [188] | |
Rapamycin | Breast cancer | It promotes intracellular autophagy and boosts the function of Atg7 and DAPK via transcriptional activation | [196] | ||
Griseofulvin | Colorectal and cervical cancers | Affects microtubule assembly in MCF-7 cells, causing programmed cell death ↑Cell cycle arrest | |||
Clotrimazole | Breast, colon and pulmonary cancer | Blockes actin polymerization and activates glycolytic inflow | [203] | ||
Ciclopirox | Breast, colorectal cancer rhabdomyosarcoma | ↓CDC–CDK, ↓Bcl-XL ↑Caspase-dependent cascade causing apoptotic cell death | |||
Nannocystin A | Colorectal and breast cancer cells | Target eukaryotic elongation factor 1 in proteome investigations | |||
NSAIDS drugs | Aspirin | Hepatocellular carcinoma | Affects P4HA2 by suppressing NF-κB and LMCD1-AS1/let-7g of Aspirin prevents tumour growth and accumulation of collagen | ||
Ibuprofen | Adenocarcinoma | Modulates the expression levels of cancer-related genes Akt, P53, PCNA, Bax, and Bcl2 | [228] | ||
Naproxen | bladder carcinoma | ↑Cell arrest ↑Cancer cells death ↑PI3K | [233] | ||
Diclofenac | Ovarian cancer | ↑Apoptotic cell death ↓SOD2 ↓Proportion of free radicals | |||
Celecoxib | Bladder cancer | Blocks epithelial-to-mesenchymal transformation ↓miRNA-145/TGFBR2/Smad3 axis | [250] | ||
Indomethacin | Colon cancer | ↓Cancer cell proliferation ↓PKC-p38-DRP1 ↓Wnt/-βcatenin signalling, to effectively target MAPK mechanisms | |||
Thiocolchicoside | Leukaemia, lymphoma, and squamous cell carcinoma | Blocks the receptor stimulator NF-kB ligand ↓NF-kB signalling cascade ↓Cancer-induced bone metastasis | |||
Artemisinin | Breast cancer | Deactivates cancer-related fibroblasts and decreases CAFs mediating growth and metastases by suppressing TGF-β signalling | [315] | ||
Artesunate | Hepatocellular carcinoma | ↑Pro-apoptotic proteins ↑caspases ↓MYC oncogene ↓Anti-apoptotic proteins | |||
Dihydroartemisinin | Ovarian cancer | ↓Cancer cell development ↓Metastases by addressing the platelet-derived growth factor receptor-alpha (PDGFR) | [316] | ||
Mebendazole | Melanoma | ↑Apoptotic cell death ↑Caspases ↑Bcl-2 ↓Repressor of apoptosis X-linked blocker of apoptosis (XIAP) | |||
Chloroquine | Metastatic tumors | Par-4-dependent suppression, mediates p53- and Rab8b-based Par-4 production to promote tumour cell death | [279] | ||
Pyrimethamine | Non-small cell lung cancer | ↓EMT ↓Invasion ↓Cancer cells growth, ↓Metastases by interacting with dihydrofolate reductase and thymidine phosphorylase | |||
Quinacrine | Renal cancer | Facilitates chromatin transcription (FACT) protein complex, which seems to be trapped on chromatin and induces CK2-induced phosphorylation of p53, responsible for quinacrine-mediated p53 transcription |