Phytochemical Name : Extract of Spondias pinnata

Properties Information
PhytoCAT-ID PhytoCAT-738
Phytochemical name or plant extracts Extract of Spondias pinnata
PMID 23686547
Literature evidence Flow cytometric analysis and confocal microscopic studies confirmed that SPME is able to induce apoptosis in both malignant cell lines.
IUPAC name NA
Phytochemicals’ class or type of plant extracts Methanolic extract
Source of phytochemicals or plant Extracts Spondias pinnata
Geographical availability Andaman Is., Assam, Bangladesh, China South-Central, China Southeast, East Himalaya, Hainan, India, Jawa, Laos, Lesser Sunda Is., Malaya, Maluku, Myanmar, Nepal, Pakistan, Philippines, Sri Lanka, Sulawesi, Thailand, Vietnam
Plant parts Bark
Other cancers Breast cancer, Lung cancer
Target gene or protein Caspase 3, Caspase 9, PARP, Bax
Gene or Protein evidence The 17 kDa subunit of cleaved caspase-3 was clearly detected after 8 h of treatment in A549 and MCF-7 cells followed by a gradual increase in its level. The 17 kDa subunit of cleaved caspase-9 was found increasing with time in both types of cells. the expression of Bax was also found increasing in MCF-7 cell with no change in expression of Bcl-2.
Target pathways Death-receptor-induced extrinsic pathway , mitochondria-apoptosome-mediated intrinsic pathway
IC50 149.34 ± 13.30 μg/ml against MCF-7
Potency SPME inhibited the growth of both A549 and MCF-7 cells in a dose-dependent manner with an IC50 value of 147.84 ± 3.74 and 149.34 ± 13.30 μg/ml, respectively.
Cell line/ mice model MCF-7, A549
Additional information  SPME increased the number of cells in sub-G1 phase both in the case of A549 and MCF-7 dose dependently, which refers to the cells that underwent apoptosis. This sub-G1 population was quantified as the percentage of apoptosis. These results indicate SPME induced cell death in A549 and MCF-7 cells.
PubChem ID NA
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:71489-1
Safety The cytotoxicity of SPME on the normal fibroblast cell line was also evaluated, the results showed that treatment of WI-38 with the extract did not inhibit the cell proliferation significantly and the IC50 was calculated as 932.38 ± 84.44 μg/ml