Review Article

Chemical Constituents and Pharmacological Activities of Steroid Saponins Isolated from Rhizoma Paridis

Table 1

Efficacy of Rhizoma Paridis-derived steroid saponins against cancer in vitro.

CompoundCell line and IC50Targeting pathwaysRef.

Polyphyllin DHepG2 (4.01 uM, 24 h)Fas and JNK pathways; p53-Bax/Bcl-2 and p53-p21-cyclin E/CDK2 pathways; NF-kB and MMP-9[21]
Bel-7402 (4.74 uM, 24 h)[25,26]
PC-9 (2.69 μg/ml, 48 h)Bcl-2/Bax[34]
PC-9-ZD (2.51 μg/ml, 24 h; 2.07 μg/ml, 48 h; 1.53 μg/ml, 72 h)Bax/Bcl-2-caspase-3[35]
Hela (2.62 μM, 24 h)Bcl-2/Bax-caspase-3/9[36]

Pb/formosanin CHepG2 (13.62 ug/mL, 24 h; 3.29 ug/mL, 48 h)NMR metabolic pathways[22]
Bel-7402 (4.36 uM, 24 h)p53-Bax/Bcl-2 and p53-p21-cyclin E/CDK2 pathways; NF-kB and MMP-9[25,26]
SKOV3 (20.99 uM,24 h; 10.44 uM, 48 h; 8.83 uM, 72 h)NF-κB-VEGF and NF-κB-Bcl-2/Bcl-xL[27]
CaSki (5.7 μM), SiHa (3.7 μM), HEC-1A (2.1 μM), and A549 (4.0 μM)Bax-caspase-3/9 and ERK/Bcl-2[28]
HOC-7 (6.44 uM, 48 h)VEGF[30]
NCI–H460 (2.0 μM, 48 h) and NCI–H520 (1.6 μM, 48 h)JNK pathway[32]

Compound 1HepG2 (2.35 uM, 48 h)Mitochondrial apoptotic, CDK1, PI3K/Akt, and MAPK pathways[23]
MCF-7 (2.59 uM, 48 h)
PC-3 (4.76 uM, 48 h)

Polyphyllin VIIHepG2 (1.77 uM, 48 h),Mitochondrial apoptotic, CDK1, PI3K/Akt, and MAPK pathways[23]
MCF-7 (2.71 uM, 48 h),
PC-3 (4.67 uM, 48 h)
A2780 (3.0 μM, 24 h) and SKOV3 (3.0 μM, 24 h)PP2A/AKT/DRP1 signaling axis[29]

Polyphyllin VISCC-15 (25.80 μM, 24 h; 21.22 μM, 48 h; 19.57 μM, 72 h)p38/p53 and caspase 3/8 pathways[38]

Paris saponin HU251 (100 μg/ml, 48 h)ARA1/ARA3 and Akt/MAPK[40]