Background:
Breast carcinoma is a malignant disease that represents the most common
non-skin malignancy and a chief reason of cancer death in women. Large interest is growing in the
use of natural products for cancer treatment, especially with goal of suppression angiogenesis, tumor
cell growth, motility, as well as invasion and metastasis with low/no toxicity. It is evident
from recent patents on the anticancer properties of sesquiterpene lactones such as parthenolide.
Objective:
In this study, using MDA-MB-231 cells of a human breast adenocarcinoma, the effects
of aguerin B, as a natural sesquiterpene lactone, has been evaluated, in terms of the expression of
metastatic-related genes (Pak-1, Rac-1 and HIF-1α).
Methods:
Cytotoxicity of aguerin B was tested toward MDA-MB-231 breast tumor cells using
MTT. Scratch assay was accomplished to evaluate the tumor cell invasion. To understand the underlying
molecular basis, the mRNA expressions were evaluated by real time PCR.
Results:
It was found that aguerin B significantly inhibited human breast cancer cell growth in
vitro (IC50 = 2μg/mL) and this effect was accompanied with a persuasive suppression on metastasis.
Our results showed that aguerin B in IC50 concentration down-regulated Rac-1, Pak-1, Hif-1α
and Zeb-1 transcriptional levels.
Conclusion:
Taken together, this study demonstrated that aguerin B possessed potential anti-metastatic
effect, suggesting that it may consider as a potential multi target bio compound for treatment
of breast metastatic carcinoma.
Synthesis, Characterization, and Study of In Vitro Cytotoxicity of ZnO-Fe3O4 Magnetic Composite Nanoparticles in Human Breast Cancer Cell Line (MDA-MB-231) and Mouse Fibroblast (NIH 3T3)
