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The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

Site-Specific Anticancer Effects of Dietary Flavonoid Quercetin

Sak, Katrin·2014·Nutrition and Cancer

Abstract

Food-derived flavonoid quercetin, widely distributed in onions, apples, and tea, is able to inhibit growth of various cancer cells indicating that this compound can be considered as a good candidate for anticancer therapy. Although the exact mechanism of this action is not thoroughly understood, behaving as antioxidant and/or prooxidant as well as modulating different intracellular signalling cascades may all play a certain role. Such inhibitory activity of quercetin has been shown to depend first of all on cell lines and cancer types; however, no comprehensive site-specific analysis of this effect has been published. In this review article, cytotoxicity constants of quercetin measured in various human malignant cell lines of different origin were compiled from literature and a clear cancer selective action was demonstrated. The most sensitive malignant sites for quercetin revealed to be cancers of blood, brain, lung, uterine, and salivary gland as well as melanoma whereas cytotoxic activity was higher in more aggressive cells compared to the slowly growing cells showing that the most harmful cells for the organism are probably targeted. More research is needed to overcome the issues of poor water solubility and relatively low bioavailability of quercetin as the major obstacles limiting its clinical use.

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Metadata

Authors
Sak, K.
Venue
Nutrition and Cancer
Published
2013-12-30
Volume
66
Issue
2
Pages
177-193
ISSN
  • 0163-5581 (ISSN-L)
  • 1532-7914
OpenAlex
W2015199985
Cited by
170
References
4
FWCI
9.77
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Site-Specific Anticancer Effects of Dietary Flavonoid Quercetin. https://app.cochat.ai/papers/10.1080/01635581.2014.864418
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Sak, K. (2014). Site-Specific Anticancer Effects of Dietary Flavonoid Quercetin. Nutrition and Cancer. https://doi.org/10.1080/01635581.2014.864418

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