Table 3.
PharmacologicalEffects | Chemical component | Mechanism | Cell Lines/Model | Dosage of Administration | Ref. |
---|---|---|---|---|---|
Anticancer | H11 | Inhibiting growth | subcutaneous mouse sarcoma S180 | 4 and 8 mg·kg-1 | (Kanayama et al., 1986) |
Pi-PCM0, Pi-PCM1 and Pi-PCM2 | inhibiting proliferation | Sarcoma 180 grown in mice |
20 mg·kg-1 | (Huang et al., 2007) | |
PCM3-II | Reducing proliferation and viability and inducing cell-cycle G1 arrest | human breast carcinoma MCF-7 cells | 400 μg·ml-1 | (Zhang et al., 2006) | |
ac-PCM2 and wc-PCM2 | inhibiting growth |
Sarcoma 180 solid tumor grown in BALB/c mice | 20 mg·kg-1 | (Jin et al., 2003b) | |
CS-PCS3-II | increasing necrosis and apoptosis and immunological responses in tumor cells | Sarcoma 180 solid tumor grown in BALB/c mice | 20 mg·kg-1 | (Chen et al., 2010) | |
S1- S6 | inducing and facilitating apoptosis | HepG2 and S-180 tumor cells | 20 mg·kg-1 | (Huang et al., 2006) | |
WSP, WSP-1 and WSP-2 | anti-proliferation | S180 tumor cells | 100 and 200 mg·kg-1 | (Bian et al., 2010) | |
CMP33 | inhibiting growth | MCF-7, A549, HepG-2 and SGC-7901 cells | 1 mg·ml-1 | (Liu et al., 2019) | |
Dehydropachymic acid and Dehydroeburicoic acid | anti-proliferative activity | Molt 4 and HL 60 cells | – | (Lai et al., 2016) | |
Pachymic acid | inducing apoptosis by resulting in mitochondria dysfunction | DU145 cells | 40 mg·kg-1 | (Zhang et al., 2005) | |
Pachymic acid | inhibiting-proliferation by activating caspase 3, up-regulating PTEN expression and reducing AKT phosphorylation | primary osteosarcoma cells | 10–50 μg·ml-1 | (Wen et al., 2018) | |
Pachymic acid | Inhibiting proliferation and inducing apoptosis by up-regulating the expression of DNA damage-related proteins | NPC cells | 10–30 μM | (Zhang et al., 2017) | |
Pachymic acid | Decreased cell viability | SGC-7901 and MKN-49P cells | 15–240 μmol·L-1 | (Lu et al., 2017) | |
Anti-Oxidant | PCP-H, PCP-U, PCP-E and PCP-M | reducing and scavenging hydroxyl and DPPH radicals | – | – | (Wang et al., 2016) |
PCP-1, PCP-2 and PCP-3 | scavenging hydroxyl radicals, ABTS radicals and ferrous ions | – | – | ||
Anti-inflammatory | PC-II | inhibiting the production of IP-10 induced by IFN-γ | (Lu et al., 2010) | ||
CMP33 | improving colitis by decreasing levels of pro-inflammatory cytokines and increasing levels of anti-inflammatory cytokines | mice with inflammatory bowel disease (IBD) | (Liu et al., 2018) | ||
Pachymic acid, Trametenolic acid and Polyporenic acid C | inhibiting NO production and iNOS expression | RAW 264.7 cells | (Lee et al., 2017) | ||
Immunomodulation | PCWPW and PCWPS | inhibited T cell proliferation | PC12 cells | (Zhang et al., 2018) | |
S-P, CMP and S-CMP | Increasing hemolysin antibody titer and antibody | implanted HepG2 tumor in BALB/c mice | (Wang W. et al., 2015) | ||
Kidney protection | Poricoic acid ZL, ZI and ZK | down-regulating profibrotic protein expression | HK-2, NRK-52E and NRK-49F cells | (Chen L. et al., 2019) | |
Poricoic acid A | decreasing the elevated levels of creatinine and urea and improving renal fibrosis and podocyte injury | rats and renal NRK-52E cells | (Chen D. et al., 2019) | ||
Liver protection | PCPs | decreasing the levels of ALT, LD, TNF-α and IL-6 | liver injury mice induced by APAP | (Wu et al., 2018) |