Phytochemical Name : Anacardic acid

Properties Information
PhytoCAT-ID PhytoCAT-614
Phytochemical name or plant extracts Anacardic acid
PMID 26990649
Literature evidence Since mitochondrial-targeted anticancer therapy (mitocans) may be useful in breast cancer, we examined the effect of anacardic acid on cellular bioenergetics and OXPHOS pathway proteins in breast cancer cells modeling progression to endocrine-independence: MCF-7 estrogen receptor ? (ER?)+ endocrine-sensitive, LCC9 and LY2 ER?+, endocrine-resistant, and MDA-MB-231 triple negative breast cancer (TNBC) cells.
IUPAC name 2-hydroxy-6-pentadecylbenzoic acid
Phytochemicals’ class or type of plant extracts Phenolic acid
Source of phytochemicals or plant Extracts Anacardium occidentale
Geographical availability Bolivia, Brazil North, Brazil Northeast, Brazil Southeast, Brazil West-Central, Colombia, Ecuador, Guyana, Peru, Suriname, Trinidad-Tobago, Venezuela
Plant parts Nutshell
Other cancers Breast cancer
Target gene or protein SCD, INSIG1,TGM2, PDK4, GPR176, ZBT20, GRP78, Hsp70, CDK-4, MMP9, Bcl-2, Mcl-1 , miR-378g, Cyclin D1, MYC, c-FOS, PPARγ, SIN3
Gene or Protein evidence Only six genes were commonly altered by AnAc in both cell lines: SCD, INSIG1, and TGM2 were decreased and PDK4, GPR176, and ZBT20 were increased. Regulation of the key Hsp90-dependent tumor-related molecules or endoplasmic reticulum stress (ERS) related molecules, such as GRP78, Hsp70, CDK-4, MMP-9, Bcl-2, and Mcl-1 by AA may be related to these effects. AnAc reduced miR-378g that targets VIM (vimentin) and VIM mRNA transcript expression was increased in AnAc-treated MCF-7 cells, suggesting a reciprocal relationship. The pathways modulated by these AnAc-regulated miRNAs suggest that key nodal molecules, e.g., Cyclin D1, MYC, c-FOS, PPARγ, and SIN3, are targets of AnAc activity.
Target pathways VEGF signaling pathway
IC50 13.5 µM against MCF-7 35 µM against MDA-MB-231
Potency Anacardic acid (AnAc) is a dietary phenolic lipid that inhibits both MCF-7 estrogen receptor α (ERα) positive and MDA-MB-231 triple negative breast cancer (TNBC) cell proliferation with IC50s of 13.5 and 35 μM, respectively.
Cell line/ mice model MDA-MB-231, MCF-7
Additional information  Taken together, our results suggest that AA shows potential as a possible new drug for therapy of TNBC.
PubChem ID 167551
Additional PMIDs 25788052 28886127 30210681
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:319068-2
Safety NA