| Literature DB >> 27081641 |
Guilherme di Camillo Orfali1, Ana Carolina Duarte1, Vivien Bonadio1, Natalia Peres Martinez1, Maria Elisa Melo Branco de Araújo1, Fernanda Bruschi Marinho Priviero1, Patricia Oliveira Carvalho1, Denise Gonçalves Priolli1.
Abstract
This review was based on a literature search of PubMed and Scielo databases using the keywords "quercetin, rutin, isoquercitrin, isoquercitin (IQ), quercetin-3-glucoside, bioavailability, flavonols and favonoids, and cancer" and combinations of all the words. We collected relevant scientific publications from 1990 to 2015 about the absorption, bioavailability, chemoprevention activity, and treatment effects as well as the underlying anticancer mechanisms of isoquercitin. Flavonoids are a group of polyphenolic compounds widely distributed throughout the plant kingdom. The subclass of flavonols receives special attention owing to their health benefits. The main components of this class are quercetin, rutin, and IQ, which is a flavonoid and although mostly found as a glycoside, is an aglycone (lacks a glycoside side chain). This compound presents similar therapeutic profiles to quercetin but with superior bioavailability, resulting in increased efficacy compared to the aglycone form. IQ has therapeutic applications owing to its wide range of pharmacological effects including antioxidant, antiproliferative, anti-inflammatory, anti-hypertensive, and anti-diabetic. The protective effects of IQ in cancer may be due to actions on lipid peroxidation. In addition, the antitumor effect of IQ and its underlying mechanism are related to interactions with Wnt signaling pathway, mixed-lineage protein kinase 3, mitogen-activated protein kinase, apoptotic pathways, as well proinflammatory protein signaling. This review contributed to clarifying the mechanisms of absorption, metabolism, and actions of IQ and isoquercitrin in cancer.Entities:
Keywords: Antioxidants; Antitumor; Cancer; Drug screening assays; Flavonoids; Flavonols; Neoplasms
Year: 2016 PMID: 27081641 PMCID: PMC4826964 DOI: 10.5306/wjco.v7.i2.189
Source DB: PubMed Journal: World J Clin Oncol ISSN: 2218-4333