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 |