Properties | Information | |
---|---|---|
PhytoCAT-ID | PhytoCAT-1033 | |
Phytochemical name or plant extracts | Lentinula edodes mycelia extract | |
PMID | 23874107 | |
Literature evidence | Concomitant use of LEM(Lentinula edodes mycelia extract) with FEC75 therapy can maintain host QOL and immune function, and offer important implications for an application of LEM as a useful oral adjuvant to anthracycline-based chemotherapies. | |
IUPAC name | NA | |
Phytochemicals’ class or type of plant extracts | Mycelia extract | |
Source of phytochemicals or plant Extracts | Lentinula edodes | |
Geographical availability | East Asia(mainly in China and Japan) | |
Plant parts | NA | |
Other cancers | Breast cancer | |
Target gene or protein | SOD1 | |
Gene or Protein evidence | Immunohistochemical assessment of SOD1 as markers of inflammation and oxidative stress were performed. | |
Target pathways | TLR4/Dectin1-MAPK and Syk-PKC-NF-κB pathways | |
IC50 | NA | |
Potency | Subjects were treated with two courses of FEC75 chemotherapy (5-fluorouracil [5-FU], 500 mg/m2, cyclophosphamide, 500 mg/m2, epirubicin, 75 mg/m2) for 3 weeks as one course. The first course comprised FEC75 chemotherapy alone, whereas the second course used LEM in combination with FEC. In the second course, subjects took 1800 mg/day of LEM every day for the 3 weeks. | |
Cell line/ mice model | MCF-7 and MDA-MB-231 cells. | |
Additional information | Latcripin-7a, derivative of Lentinula edodes c(91-3), reduces migration and induces apoptosis, autophagy, and cell cycle arrest at G-(1) phase in breast cancer cells. | |
PubChem ID | NA | |
Additional PMIDs | 19020765 33044599 | |
Additional sources of information | http://bioweb.uwlax.edu/bio203/s2007/hendzel_abby/Habitat.htm#:~:text=Lentinula%20edodes%20is%20native%20to,of%20the%20mushroom's%20life... | |
Safety | NA |