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Flavonoids and Gastric Cancer Therapy: From Signaling Pathway to Therapeutic Significance.

Authors :
Cai J
Tan X
Hu Q
Pan H
Zhao M
Guo C
Zeng J
Ma X
Zhao Y
Source :
Drug design, development and therapy [Drug Des Devel Ther] 2024 Jul 25; Vol. 18, pp. 3233-3253. Date of Electronic Publication: 2024 Jul 25 (Print Publication: 2024).
Publication Year :
2024

Abstract

Gastric cancer (GC) is a prevalent gastrointestinal tumor characterized by high mortality and recurrence rates. Current treatments often have limitations, prompting researchers to explore novel anti-tumor substances and develop new drugs. Flavonoids, natural compounds with diverse biological activities, are gaining increasing attention in this regard. We searched from PubMed, Web of Science, SpringerLink and other databases to find the relevant literature in the last two decades. Using "gastric cancer", "stomach cancers", "flavonoid", "bioflavonoid", "2-Phenyl-Chromene" as keywords, were searched, then analyzed and summarized the mechanism of flavonoids in the treatment of GC. It was revealed that the anti-tumor mechanism of flavonoids involves inhibiting tumor growth, proliferation, invasion, and metastasis, as well as inducing cell death through various processes such as apoptosis, autophagy, ferroptosis, and pyroptosis. Additionally, combining flavonoids with other chemotherapeutic agents like 5-FU and platinum compounds can potentially reduce chemoresistance. Flavonoids have also demonstrated enhanced biological activity when used in combination with other natural products. Consequently, this review proposes innovative perspectives for the development of flavonoids as new anti-GC agents.<br />Competing Interests: All authors declare that there are no conflicts of interest and agree to publish this paper.<br /> (© 2024 Cai et al.)

Details

Language :
English
ISSN :
1177-8881
Volume :
18
Database :
MEDLINE
Journal :
Drug design, development and therapy
Publication Type :
Academic Journal
Accession number :
39081701
Full Text :
https://doi.org/10.2147/DDDT.S466470