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Review
. 2020 Aug;34(8):1812-1828.
doi: 10.1002/ptr.6647. Epub 2020 Feb 14.

Apigenin as an anticancer agent

Affiliations
Review

Apigenin as an anticancer agent

Muhammad Imran et al. Phytother Res. 2020 Aug.

Abstract

Apigenin is an edible plant-derived flavonoid that has been reported as an anticancer agent in several experimental and biological studies. It exhibits cell growth arrest and apoptosis in different types of tumors such as breast, lung, liver, skin, blood, colon, prostate, pancreatic, cervical, oral, and stomach, by modulating several signaling pathways. Apigenin induces apoptosis by the activation of extrinsic caspase-dependent pathway by upregulating the mRNA expressions of caspase-3, caspase-8, and TNF-α. It induces intrinsic apoptosis pathway as evidenced by the induction of cytochrome c, Bax, and caspase-3, while caspase-8, TNF-α, and B-cell lymphoma 2 levels remained unchanged in human prostate cancer PC-3 cells. Apigenin treatment leads to significant downregulation of matrix metallopeptidases-2, -9, Snail, and Slug, suppressing invasion. The expressions of NF-κB p105/p50, PI3K, Akt, and the phosphorylation of p-Akt decreases after treatment with apigenin. However, apigenin-mediated treatment significantly reduces pluripotency marker Oct3/4 protein expression which might be associated with the downregulation of PI3K/Akt/NF-κB signaling.

Keywords: apigenin; breast cancer; flavonoids; glioblastoma; liver cancer; pancreatic cancer; prostate cancer.

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References

REFERENCES

    1. Babcook, M. A., & Gupta, S. (2012). Apigenin modulates insulin-like growth factor axis: Implications for prevention and therapy of prostate cancer. Current Drug Targets, Advance online publication.
    1. Bai, H., Jin, H., Yang, F., Zhu, H., & Cai, J. (2014). Apigenin induced MCF-7 cell apoptosis-associated reactive oxygen species. Scanning, 36(6), 622-631. https://doi.org/10.1002/sca.21170
    1. Banerjee, K., & Mandal, M. (2015). Oxidative stress triggered by naturally occurring flavone apigenin results in senescence and chemotherapeutic effect in human colorectal cancer cells. Redox Biology, 5, 153-162. https://doi.org/10.1016/j.redox.2015.04.009
    1. Bao, Y. Y., Zhou, S. H., Lu, Z. J., Fan, J., & Huang, Y. P. (2015). Inhibiting GLUT-1 expression and PI3K/Akt signaling using apigenin improves the radiosensitivity of laryngeal carcinoma in vivo. Oncology Reports, 34(4), 1805-1814. https://doi.org/10.3892/or.2015.4158
    1. Bauer, D., Mazzio, E., & Soliman, K. F. A. (2019). Whole Transcriptomic analysis of Apigenin on TNFα Immuno-activated MDA-MB-231 breast cancer cells. Cancer Genomics & Proteomics, 16(6), 421-431. https://doi.org/10.21873/cgp.20146