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Updated: Apr 20, 2026

Studying Pancreatic Cancer Stem Cell Characteristics for Developing New Treatment Strategies
Published on: June 20, 2015
Role of flavonoids in future anticancer therapy by eliminating the cancer stem cells
1NGO Praeventio, Näituse 22- 3, Tartu 50407, Estonia. katrin.sak.001@mail.ee.
Abstract:
Despite the numerous recent advances made in conventional anticancer therapies, metastasis and recurrence still remain the major problems in cancer management. The current treatment modalities kill the bulk of the tumor, leaving cancer stem cells behind and therefore, the agents specifically targeting this cancer initiating cell population may have important clinical implications. In this review article, the data about the inhibitory action of flavonoids, both natural as well as their synthetic derivatives, on the self-renewal capacity and survival of cancer stem cells of different origins are compiled and analyzed. These data indicate that several plant secondary metabolites, including soy isoflavone genistein, green tea catechins and a widely distributed flavonol quercetin, have the potential to suppress the stemness markers and properties, traits of the epithelial-to-mesenchymal transition and migratory characteristics, being also able to sensitize these cells to the standard chemotherapeutic drugs. These polyphenolic compounds act through multiple signal transduction pathways, providing thus the maximal therapeutic response and offering some promise to be included in the future cancer treatment schemes in combination with the conventional therapies. Such approach may give an important contribution to the shift of cancer management from palliative to curative mode, likely leading to the disease-free survival. Thus, flavonoids can serve as attractive candidates for novel anticancer agents by eliminating the roots of cancer.
Insights
Flavonoids show promise in eliminating cancer stem cells, which drive tumor recurrence. These natural compounds can suppress cancer stem cell properties and sensitize them to chemotherapy, offering a new avenue for curative cancer treatment.
Area of Science:
- Biochemistry
- Oncology
- Pharmacology
Background:
- Metastasis and recurrence remain significant challenges in conventional cancer therapy.
- Current treatments often spare cancer stem cells (CSCs), which are responsible for tumor initiation and relapse.
- Targeting CSCs is crucial for improving cancer management and achieving disease-free survival.
Purpose of the Study:
- To review and analyze the inhibitory effects of flavonoids on cancer stem cell self-renewal and survival.
- To explore the potential of natural and synthetic flavonoids as anticancer agents targeting CSCs.
Main Methods:
- Compilation and analysis of existing data on flavonoid action against CSCs from various origins.
- Review of studies investigating the impact of flavonoids on stemness markers, epithelial-to-mesenchymal transition (EMT), and cell migration.
- Examination of flavonoid-induced sensitization of CSCs to conventional chemotherapy.
Main Results:
- Flavonoids, including genistein, catechins, and quercetin, demonstrate the ability to suppress CSC stemness markers and properties.
- These compounds inhibit EMT traits and migratory characteristics of CSCs.
- Flavonoids sensitize CSCs to standard chemotherapeutic drugs, enhancing their efficacy.
- Flavonoids act via multiple signal transduction pathways, suggesting broad therapeutic potential.
Conclusions:
- Flavonoids are promising candidates for novel anticancer therapies due to their CSC-targeting capabilities.
- Combining flavonoids with conventional treatments may lead to a shift from palliative care to curative strategies.
- Flavonoid-based therapies hold potential for achieving long-term disease-free survival by eliminating the root cause of cancer.
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