Abstract
Background
Drosera spatulata is a source of many compounds such as naphthoquinones, phenolic acids, flavonoids, anthocyanins, and naphthalene derivatives. Unfortunately, the information regarding the biological activity and chemical profile of those compounds is still incomplete. Herein, we investigated the biological activity of 3-O-acetylaleuritolic acid (3-O-AAA) in cancer cell lines.
Methods
The cell viability of HeLa, HT-29, MCF7, and MCF12A cells was assessed using MTT assay. Proliferation potential was assessed using the clonogenic assay and flow cytometry. Migration modulation was tested using a scratch assay. Protein expression was analyzed by immunoblotting.
Results
3-O-AAA significantly inhibited the growth of all tested tumor cells. The results of the colony formation assay suggested cytostatic properties of the studied compound. The scratch assay showed that 3-O-AAA was an efficient migration inhibitor in a dose-dependent manner. Moreover, it caused modulation of mTOR, beclin1, and Atg5 proteins suggesting a possible role of the compound in autophagy induction.
Conclusion
Collectively, these results demonstrated that 3-O-AAA inhibited the proliferation and migration of cancer cell lines as well as contributed to autophagy induction showing some anticancer properties.
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Abbreviations
- 3-O-AAA:
-
3-O-acetylaleuritolic acid
- CPT:
-
Camptothecin
- DMSO:
-
Dimethyl sulfoxide
- MTT:
-
3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide
- NMR:
-
Nuclear magnetic resonance
- PBS:
-
Phosphate-buffered saline
- PCNA:
-
Proliferating cell nuclear antigen
- WB technique:
-
Western blot technique
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Acknowledgements
This work was supported by the Poznan University of Medical Sciences, Grant Nos. 502-01-03318432-08035 and 502-14-03303407-09493.
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ET planned experiments, was involved in the MTT and trypan blue test, Western blot analysis, the migration assay, and wrote the manuscript. AR contributed to the Western blot and statistical analyses. MK was involved in the flow cytometry analysis. NK and BR participated in the clonogenic assay. NL and APJ were involved in the preparation of the reagents/materials. IK and JB performed the extraction of 3-O-AAA acid from the cultures of Drosera spatulata, and MR and BR contributed to the conception and supervision of the study.
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Toton, E., Kedziora, I., Romaniuk-Drapala, A. et al. Effect of 3-O-acetylaleuritolic acid from in vitro-cultured Drosera spatulata on cancer cells survival and migration. Pharmacol. Rep 72, 166–178 (2020). https://doi.org/10.1007/s43440-019-00008-x
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DOI: https://doi.org/10.1007/s43440-019-00008-x