Table 2.
Properties | Models | Mechanism | Reference |
---|---|---|---|
Apoptosis | Myeloid leukemia K562 cells | Releases cytochrome c from mitochondria, PARP and caspase-9 cleavages | [93] |
Melanoma A375 cells | Induces ROS burst, decreases GSH, and wrecks MMP | [94] | |
Gastric cancer BGC-823 cells | Induces ROS, activates ASK1, and phosphorylates JNK protein | [95] | |
Leukemic Jurkat and K562 cells | Downregulates IAPs, pAkt, c-Myc, and cyclin D1 | [96] | |
Breast cancer MCF-7, MDAMB, HepG2 cells | Generates ROS | [97] | |
Cell cycle arrest | Breast cancer MCF-7 cells | Downregulates cyclin B1, Cdc2 and NF-κB by decreasing the interaction of pIκB-NF-κB | [98] |
Cell cycle arrest and apoptosis | HT-29 colon cancer cells | Induced ROS generation, DNA fragmentation, chromatin condensation, and nuclear shrinkage | [99] |
K562 cells and xenograft mouse | Derivative PGV-1 induces prometaphase arrest in the M phase and induces cell senescence and death by increasing ROS. | [100] | |
Prostate carcinoma PC-3 and DU145 and xenograft mice |
Analogue Ca 37 induces ROS production | [101] | |
Prostate cancer RM-1 and DU145 cell lines and xenograft mice | Analog WZ35 induces ROS overproduction, intracellular calcium surge, and mitochondrial disruption | [102] | |
NCI-H460 cells | Analogues hexamethoxy-diarylpentadienones (1 and 2) upregulate p53 and p21 and downregulate Cdc25C, cyclin B1/Cdk1 in a Michael acceptor- and ROS-dependent fashion | [103] | |
NSCLC A549 and SPC-A1 cell lines | Causes ROS production, DNA damage, endoplasmic reticulum stress and mitochondrial instability. | [92] | |
Chemosensitization | Glioblastoma | DMC synergistically increases TMZ-induced apoptosis by increasing ROS production, inactivating JAK/STAT3 signaling pathway and caspase-3 cleavage | [104] |
Anti-tumorigenesis | CML-derived K562 cells, xenograft mouse | Derivatives upregulate ROS levels, compete with co-enzymes to bind to the respective ROS metabolic enzymes and inhibit their activities | [105] |
Anti-angiogenesis | HUVECs, CAMs | Analog A2 induces NADH/NADPH oxidase-derived ROS | [106] |
Tumor re-incidence and metastasis inhibition | B16F10 cells, syngeneic mice | Nanoformulation increases intracellular curcumin accumulation and ROS formation | [107] |
Anti-tumorigenesis | Gastric cancer BGC-823 cells, xenograft mice | Enhances oxidative stress, decreases mtDNA content and DNA polymerase γ | [91] |
Leukemic K562 cells, xenograft mice | Induces ROS level | [108] | |
Autophagy and apoptosis | lymphoma HuT-78 cells | Produces ROS, inhibits c-FLIP, Bcl-xL, cIAP, XIAP, disrupts the integrity of IKK and beclin-1 by degrading Hsp90, inhibits NF-κB, accumulates autophagy marker LC3-I | [109] |
Autophagy | Colon cancer HCT116 cells | Generates ROS, converts autophagic marker LC3-I to LC3-II and degrades sequestome-1 | [110] |
MMP—matrix metallopeptidase, ASK1—apoptosis signal-regulating kinase 1, IAPs—inhibitors of apoptosis proteins, JAK—Janus kinase, STAT3—signal transducer and activator of transcription 3, mtDNA—mitochondrial DNA, GSH—glutathione, ROS—reactive oxygen species.