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Glycosidic flavonoids and their potential applications in cancer research: a review

Abuyaseer Abusaliya; Sang Eun Ha; Pritam Bhagwan Bhosale; Hun Hwan Kim; Min Yeong Park; Preethi Vetrivel; Gon Sup Kim
Molecular & Cellular Toxicology · Vol. 18, Issue 1 · pp. 9-16 · 2022

Abstract

Purpose of review Every year, the cancer patient registry increases, and the leading cause of death in a global context. Plant-based molecules are gaining attention in cancer research due to the side effects of chemotherapy. A glycosidic derivative of flavonoid (GDF) plays a significant role in cancer proliferation mechanisms. GDF inhibits cell proliferation by elevating the expression of apoptotic proteins, altering the expression of nuclear factor-kappa B (NF- κB), and decreasing mitochondrial membrane potential (Δψm) in cancer cells. Recent findings Reported studies on the flavonoids orientin, vitexin, prunetionoside, chrysin, and scutellarein increased attention and are being widely investigated for their potential role in different parts of cancer research. Prunetionoside is a flavonoid with high cytotoxic potential and capable of inducing necroptosis in AGS gastric cancer cells. Similarly, scutellarein is a flavonol, induces an extrinsic apoptotic pathway and downregulates the expression level of cyclin proteins in HepG2 liver cancer cells. Vitexin is reported to be capable of deregulating the expression levels of p-Akt, p-mTOR, and p-PI3K in A549 lung cancer cells. Orientin inhibits IL-8 expression and invasion in MCF-7 breast cancer cells by suppressing MMP-9 in the presence of TPA via STAT3/AP-1/ERK/PKCα-mediated signaling pathways. It also induces mitochondria-mediated intrinsic apoptosis and G0/G1 cell cycle arrest in HT29 colon cancer cells. Chrysin is a flavonoid present in honey that has been shown to play an important role in cervical and colon cancer by suppressing the AKT/mTOR/PI3K pathway and increasing ROS accumulation, LDH leakage, respectively.

Bibliographic Information

JournalMolecular & Cellular Toxicology
PublisherSpringer
Publication Date2022-01-01
Publication Year2022
Volume18
Issue1
Pages9-16
Document TypeJournal Article
Print ISSN1738-642X
eISSN2092-8467
DOI10.1007/s13273-021-00178-x

Access Information

NARA Access Coverage2010-01-01~Current
Journal Homepagehttps://www.springer.com/journal/13273
Publisher PageOpen Publisher Page
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