Valerian and valeric acid inhibit growth of breast cancer cells possibly by mediating epigenetic modifications.
Study Design
- Type d'étude
- In Vitro
- Intervention
- Valerian and valeric acid inhibit growth of breast cancer cells possibly by mediating epigenetic modifications. aqueous valerian extract and valeric acid (dose- and time-dependent)
- Comparateur
- Placebo
- Direction de l'effet
- Positive
- Risque de biais
- Unclear
Abstract
Valerian root (Valeriana officinalis) is a popular and widely available herbal supplement used to treat sleeping disorders and insomnia. The herb's ability to ameliorate sleep dysfunction may signify an unexplored anti-tumorigenic effect due to the connection between circadian factors and tumorigenesis. Of particular interest are the structural similarities shared between valeric acid, valerian's active chemical ingredient, and certain histone deacteylase (HDAC) inhibitors, which imply that valerian may play a role in epigenetic gene regulation. In this study, we tested the hypothesis that the circadian-related herb valerian can inhibit breast cancer cell growth and explored epigenetic changes associated with valeric acid treatment. Our results showed that aqueous valerian extract reduced growth of breast cancer cells. In addition, treatment of valeric acid was associated with decreased breast cancer cell proliferation, migration, colony formation and 3D formation in vitro in a dose- and time-dependent manner, as well as reduced HDAC activity and a global DNA hypomethylation. Overall, these findings demonstrate that valeric acid can decrease the breast cancer cell proliferation possibly by mediating epigenetic modifications such as the inhibition of histone deacetylases and alterations of DNA methylation. This study highlights a potential utility of valeric acid as a novel HDAC inhibitor and a therapeutic agent in the treatment of breast cancer.
Full Text
Figures
Figure 1
Cell viability assays demonstrate dose-dependent growth inhibition of triple-negative breast cancer cells following valerian extract treatment.
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Figure 2
Valeric acid exposure reduces breast cancer cell proliferation in a concentration-dependent manner, as measured by colony formation and cell counting assays.
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Figure 3
Apoptosis markers and cell cycle arrest patterns in breast cancer cells treated with valerian-derived compounds are quantified, indicating increased programmed cell death.
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Figure 4
Epigenetic modification profiles, including histone acetylation changes, in breast cancer cells exposed to valeric acid are compared to untreated controls.
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Figure 5
Gene expression changes related to epigenetic regulators in valerian-treated breast cancer cells suggest HDAC inhibitory activity as a potential mechanism of anti-tumor action.
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Figure 6
Summary model of valerian and valeric acid mechanisms in breast cancer growth inhibition is presented, linking epigenetic modifications to downstream anti-proliferative effects.
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