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mTOR Targeted Cancer Chemoprevention by Flavonoids
Badar Ul Islam1, Mohd Shahnawaz Khan2, Fohad Mabood Husain3
1Department of Biochemistry, J.N Medical College, Faculty of Medicine, Aligarh Muslim University, Aligarh,, India.
Abstract:
Over the past several decades, plant-derived products (phytochemicals) have been suggested to possess immense therapeutic potential. Among these phytochemicals, different flavonoids have been reported for their potent anticancer activity. To exhibit their anticancer potential, these flavonoids modulate different signaling pathways. Among these pathways, the mammalian target of rapamycin (mTOR) and associated phosphatidyl-inositol 3-kinase (PI3K)/protein kinase B (Akt) signaling cascade have been reported as a pivotal modulator of cell survival, proliferation, and death/apoptosis. Hence, targeting this cascade could be an ideal strategy to alleviate apoptosis and inhibit proliferation in different forms of cancer. The targeting of PI3K/Akt/mTOR by flavonoids have been well documented in the scientific literature. In the current study, we have studied the anticancer potential of various flavonoids, especially flavones, flavonols, and isoflavones that include apigenin, luteolin, baicalein, tangeretin, epigallocatechin- 3-gallate, genistein, and daidzein especially dealing with mTOR targeting.
Insights
Flavonoids, plant compounds, show anticancer potential by targeting the PI3K/Akt/mTOR pathway, crucial for cancer cell survival and proliferation. This study explores specific flavonoids like apigenin and genistein for their mTOR-inhibiting effects.
Area of Science:
- Biochemistry
- Molecular Biology
- Pharmacology
Background:
- Plant-derived phytochemicals, particularly flavonoids, exhibit significant therapeutic potential, especially in cancer treatment.
- Flavonoids exert anticancer effects by modulating critical cell signaling pathways.
- The phosphatidyl-inositol 3-kinase (PI3K)/protein kinase B (Akt)/mammalian target of rapamycin (mTOR) cascade is a key regulator of cell survival and proliferation, making it a prime target for cancer therapy.
Purpose of the Study:
- To investigate the anticancer potential of various flavonoids, focusing on flavones, flavonols, and isoflavones.
- To specifically examine the role of these flavonoids in targeting the PI3K/Akt/mTOR signaling pathway.
- To evaluate specific compounds including apigenin, luteolin, baicalein, tangeretin, epigallocatechin-3-gallate, genistein, and daidzein.
Main Methods:
- Literature review on flavonoid anticancer activity and mTOR targeting.
- Analysis of signaling pathway modulation by selected flavonoids.
- Focus on the PI3K/Akt/mTOR cascade's role in cancer cell apoptosis and proliferation.
Main Results:
- Flavonoids, including flavones, flavonols, and isoflavones, demonstrate potent anticancer activities.
- These compounds effectively modulate the PI3K/Akt/mTOR signaling pathway.
- Specific flavonoids like apigenin, genistein, and epigallocatechin-3-gallate show promise in targeting this critical cancer pathway.
Conclusions:
- Flavonoids represent a promising class of natural compounds for cancer therapy.
- Targeting the PI3K/Akt/mTOR pathway with flavonoids offers a viable strategy to inhibit cancer cell proliferation and induce apoptosis.
- Further research into specific flavonoids and their mechanisms is warranted for drug development.
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