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. 2020 Nov 10;10(11):1536. doi: 10.3390/biom10111536

Table 4.

In vitro evidence of the effects of curcumin on androgen-insensitive prostate cancer cells.

Cell Line Curcumin Dosage Effects Reference
PC3 0–50 μM; 0–72 h
IC50: 10–20 μM
↓ Proliferation
↑ Lifted, round cells
[54]
DU-145 10 and 50 μM; 1–4 days to assess cell viability
0–100 μM; 5 h to assess NF-κB expression
0-50 μM; 5 h to assess AP-1 expression
50 μM; 0–72 h to assess the expression of Bcl-2 and Bcl-xL
100 μM; 0–72 h to assess the expression and activity of procaspases 3 and 8
50 μM; 0–4 days to assess cell proliferation, PARP cleavage, and apoptosis
↓ Cell viability
↓ Proliferation
↓ NF-κB protein activation
↓ AP-1 protein
↓ Bcl-2 protein
↓ Bcl- xL protein
↑ Procaspase-3 and -8 activity
↑ PARP cleavage
↑ Apoptosis
[55]
PC3 30 μM; 21 days to assess colony formation efficiency
0–50 μM; 24 h to assess cell growth
30 μM; 24 h
↓ Cell growth
↓ Colony formation efficiency
↓ AR transcriptional activity
↓ c-Jun
↓ AP-1
↓ CBP
↓ NF-κB mRNA
[56]
DU-145 5–40 μM; 48 h ↓ Cell viability
↑ Cell cycle arrest at the G2/M phase
[58]
PC3, DU-145 35 μM; 30 min in PC3
14 μM; 30 min in DU-145
↓ p-Akt in PC3 only [59]
DU-145 0–125 ug/mL; 24–72 h to assess cell proliferation
10 ug/mL; 0–48 h to assess apoptosis
0–100 ug/mL; 0–48 h to assess MMP-2 an MMP-9 secretion
1–15 ug/mL; 24 h to assess MMP-9 protein expression
↓ Proliferation
↑ Apoptosis
↓ MMP-2 secretion
↓ MMP-9 secretion
↓ MMP-9 protein
[88]
PC3 0–50 μM; 0–72 h to assess the expression of MDM2, p21, Bax, and E2F1
0–30 μM; 24 h and 15 μM; 0–20 h to assess MDM2 mRNA expression
0–30 μM; 24 h to assess ETS2 and p-Akt expression
0–30 μM; 48 h to assess apoptosis, cell viability, and proliferation
↓ Cell viability
↓ Proliferation
↓ MDM2 protein and mRNA
↑ P21
↑ Bax
↓ E2F1
↓ Bcl-2
↓ ETS2
↓ P-Akt
↑ Apoptosis
[70]
DU-145, PC3 0–30 μM; 48 h to assess cell viability
0–30 μM; 3 weeks to assess colony formation efficiency
0–30 μM; 24 h to assess caspase-3 activation and PARP cleavage
↓ Cell viability
↓ Colony formation efficiency
↑ Caspase-3 activation and nuclear translocation
↑ PARP cleavage
[61]
PC3, DU-145 20 μM in DU-145, 30 μM in PC3; 48 h to assess cell viability and NF-κB expression
20–40 μM in PC3, 10–30 μM in DU-145; 24 h to assess Akt phosphorylation
10–30 μM; 24 h to assess protein expression
↓ NF-κB
↓ IκBα
↓ Bcl-2
↓ Bcl-xL
↓ XIAP
[71]
PC3, DU-145 25 μM; 17 h
10–50 μM; 17 h to assess IL-6 and IL-8 gene expression
10–25 μM; 17 h to assess NF-κB-luc activity
↑ MKP5 mRNA
↓ TNFα
↓ P-p38
↓ COX-2
↓ COX-2 mRNA
↓ IL-6 mRNA
↓ IL-8 mRNA
↓ p38-mediated inflammatory signaling
[72]
PC3 0–30 μM; 24 h to assess cell viability
5–40 μM; 21 days to assess colony formation efficiency and TRAIL-induced apoptosis
0–10 μM; 24 h to assess expression of DR4, DR5, DcR1, an dDcR2
0–20 μM; 24 and 48 h to assess the expression of pro- and antiapoptotic proteins, caspases, cleaved PARP, and mitochondrial membrane potential
↓ Cell viability
↓ Colony formation efficiency ↑ TRAIL-induced apoptosis
↑ DR4 death receptor
↑ DR5 death receptor
↑ Bak
↑ Bax
↑ PMMA
↑ Bim
↑ Noxa
↓ Bcl-2
↓ Bcl-xL
↑ Bid cleavage to tBid
↓ IAPs
↓ XIAP
↓ Mitochondria membrane potential
↑ Caspase-3 activity
↑ Caspase-3, -8, -9 cleavage
↑ PARP cleavage
[62]
PC3 20 μM; 24 h to assess cell-cycle progression
0–20 μM; 48 h and 20 μM; 0–48 h to assess apoptotic processes
0–20 μM; 0–48 h to assess protein expression
↑ Cell-cycle arrest at the G1/S phase
↑ Apoptosis
↑ p27
↑ p21
↑ p16
↓ Rb hyperphosphorylation
↓ Cyclin D1
↓ Cyclin E
↓ CDK4
[63]
PC3 0–100 μM; 24 h ↓ Cell proliferation
↓ Glyoxalase 1 activity
↑ Cytotoxicity
↑ Necrosis
[89]
PC3 0–50 μM; 24 h to assess cell viability, 8h to assess protein and DNA synthesis
0–50 μM; 1 h and 40 μM; 0–2 h to assess protein expression
40 μM; 1 h to assess the expression of p-Akt, p-mTOR, and p-S6
↓ Proliferation
↓ p-Akt
↓ p-mTOR
↓ p70S6K
↓ FOXO1
↓ GSK3β
↑ p-AMPK
↑ MAPK
↓ Cyclin D1
↑ Phosphatase activity
[65]
PC3 30 μM; 18 h ↓ CCL2 triggered cell adhesion
↓ Cell invasion
↓ Cell motility
↓ Adhesion to fibronectin
↓ CCL2 mRNA
↓ CCL2
[90]
Pc-Bra1 10 μM, 25 μM, or 50 μM; 24 h ↓ Cell viability
↑ Apoptosis
↓ Necrosis
[75]
PC3 25, 50, and 100 μM; 24–72 h to assess apoptosis and DNA fragmentation
100 μM; 3 and 6 h to assess expression of JNK and p38 MAPK
100 μM; 48 h to assess expression of caspases and cytochrome c
↑ Apoptosis
↑ Ceramide
↑ ssDNA
↑ JNK
↑ P38 MAPK
↓ Procaspases-3, -8, and -9
↑ Accumulation of cytochrome c in cytoplasm
[66]
PC3, DU-145 10–100 μM; 4 and 24 h
20 μM; 24 h in 22RV1 and DU-145 only for fluorescent microscopy and nuclear staining
Curcumin compartmentalization within cytoplasm and exclusion from nucleus
↑ Cytotoxicity
↑ Apoptosis
↑ Autophagy
[77]
PC3 50 μM; 24 h ↓ Proliferation
Cell cycle arrest at G2/M phase
↑ Apoptosis
↓ NF-κB
↓ AP-1
[91]
PC3 20 μM; 24 h ↑ IL-6, INS, DDIT3, NDRG1, MIR-152 [81]
PC3 15 μM; 24 h ↓ Iκb kinase β
↑ IκBα
↓ CXCL1
↓ CXCL2
↓ NF-κB
[92]
PC3, DU-145, 0–50 μM; 16 h, 24 h
25 and 50 μM; 1 h acute treatments
↓ Cell growth
↓ Cell migration/invasion
↓ Total and activated matripase
[83]
PC3 0–20 μM; 48 h ↓ Cell viability
↑ Apoptosis
↓ ld1
↓ ld1 mRNA
[93]
PC3, DU-145, 40 μM; 0–24 h to assess expression of ERK1/2, SAPK/JNK
0-60 μM; 24 h to assess expression of p65 and MUC1-C
10-100 μM; 24–72 h to assess cell viability
↓ Cell viability
↑ P-ERK 1/2
↑ P-SAPK/JNK in PC3 and DU-145
↓ MUC1-C
↓ NF-κB subunit p65
[94]
PC3 25 μM ↓ EMT
↓ IL-6
↓ ROS
↓ MAOA/mTOR/HIF-1α
↓ Cell invasion
[95]
DU-145 0–50 μM; 48 h to assess cell proliferation
15 μM; 48 h
↑ Cell death
↓ HGF-induced cell scattering
↓ Wound closure
↓ Cell invasion
↑ E-cadherin
↓ Vimentin
↓ c-Met
↓ Snail mRNA
↓ p-ERK
[96]
DU-145 10–50 μM; 24–72 h to assess cell viability and apoptotic activity
25 μM; 48 h for immunoblotting and PCR
25 μM; 24–72 h to assess cell-cycle progression
↓ Proliferation
↑ Apoptosis
↓ NOTCH1
↓ Cell survival
↓ Cell growth
Cell cycle arrest at the G0/G1 stage
↑ CDK inhibitors
↑ P21
↑ P27
[97]
PC3, DU-145 0–50 μM; 24h ↑ Apoptosis
↑ Autophagy
↑ Cytotoxicity
↑ TFR1
↑ IRP1
[98]
DU-145, PC3 0–50 μM; 48 h to assess dose–response relationship
25 μM; 0–48 h to assess time–effect relationship
25 μM; 24 h for scratch assay
10 and 50 μM; 24 h for immunoblotting and PCR
↓ Cell viability
↓ Proliferation
↓ Wound closure
↓ MT1-MMP mRNA
↓ MMP2 mRNA
[99]
DU145, PC3 10 μM; 1–5 days to assess cell viability and migration
10 μM; 0–24 h for PCR and immunoblotting
10 μM; 48 h to assess PGK1 expression
↑ miR-143
↓ Proliferation
↓ Cell migration
↓ KRAS signaling
↑ Docetaxel sensitivity
↓ PGK1
↑ FOXD3
[100]
PC3 5 μg/mL; 72 h ↓ Cell viability
Cell-cycle arrest
↑ Caspase-3
↑ Uncleaved caspase-3
↑ Uncleaved caspase-9
↑ Caspase-12
↑ PARP
↑ GRP78
↑ Inositol-requiring enzyme 1
↑ Calreticulin
↑ P-eIF2α
↑ Autophagy
↑ LC3B
[67]
PC3 25 μM; 48 h to evaluate apoptosis, gene and protein expression
25 μM; 24 h to assess H2O2 production
1.6–25 μM; 48 h to assess cell viability
10–50 μM; 30 min to assess ROS production
↓ Cell viability
↑ Cytotoxicity
↑ Apoptosis
↑ ROS
↑ CuZnSOD
↑ TRX1 oxidation
↑ TRXR1 mRNA
[84]
PC3, DU-145 0–20 μM; 4 days to assess cell viability
0–10 μM; 4 days to assess proliferation, protein expression and miR-34a expression
↓ Cell viability
↓ DNA synthesis
↓ Proliferation
↓ Cyclin D1
↓ PCNA
↑ P21
↑ miR-34α
↓ β-catenin
↓ c-myc
[68]