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Molecular mechanisms underlying anticancer effects of myricetin
Kasi Pandima Devi1, Tamilselvam Rajavel1, Solomon Habtemariam2
1Department of Biotechnology, Science Block, Alagappa University, Karaikudi 630 004, Tamil Nadu, India.
Abstract:
Dietary guidelines published in the past two decades have acknowledged the beneficial effects of myricetin, an important and common type of herbal flavonoid, against several human diseases such as inflammation, cardiovascular pathologies, and cancer. An increasing number of studies have shown the beneficial effects of myricetin against different types of cancer by modifying several cancer hallmarks including aberrant cell proliferation, signaling pathways, apoptosis, angiogenesis, and tumor metastasis. Most importantly, myricetin interacts with oncoproteins such as protein kinase B (PKB) (Akt), Fyn, MEK1, and JAK1-STAT3 (Janus kinase-signal transducer and activator of transcription 3), and it attenuates the neoplastic transformation of cancer cells. In addition, myricetin exerts antimitotic effects by targeting the overexpression of cyclin-dependent kinase 1 (CDK1) in liver cancer. Moreover, it also targets the mitochondria and promotes different kinds of cell death in various cancer cells. In the present paper, a critical review of the available literature is presented to identify the molecular targets underlying the anticancer effects of myricetin.
Insights
Myricetin, a plant flavonoid, shows significant anticancer properties by targeting key cancer mechanisms and proteins. This review highlights its molecular targets for potential cancer therapies.
Area of Science:
- Phytochemistry
- Molecular Biology
- Oncology
Background:
- Myricetin is a common herbal flavonoid with recognized health benefits.
- Emerging research indicates myricetin's potential in combating human diseases, including cancer.
- It influences critical cancer hallmarks like proliferation, apoptosis, and metastasis.
Purpose of the Study:
- To critically review the literature on myricetin's anticancer effects.
- To identify the specific molecular targets responsible for myricetin's anti-cancer activity.
Main Methods:
- Literature review of scientific studies on myricetin and cancer.
- Analysis of molecular interactions and pathways affected by myricetin.
Main Results:
- Myricetin modulates cancer hallmarks such as cell proliferation, signaling pathways, apoptosis, angiogenesis, and metastasis.
- It interacts with oncoproteins including protein kinase B (PKB) (Akt), Fyn, MEK1, and JAK1-STAT3.
- Myricetin exhibits antimitotic effects by targeting cyclin-dependent kinase 1 (CDK1) in liver cancer and induces cell death via mitochondrial pathways.
Conclusions:
- Myricetin demonstrates broad-spectrum anticancer activity through diverse molecular targets.
- Its ability to interact with key oncoproteins and pathways makes it a promising candidate for cancer treatment development.
- Further research into myricetin's molecular mechanisms can pave the way for novel therapeutic strategies.
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