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Stilbene Treatment Reduces Stemness Features in Human Lung Adenocarcinoma Model
Vittoria Livraghi1, Alice Grossi1, Anna Scopelliti1
1Department of Molecular Medicine, Immunology and General Pathology Unit, University of Pavia, 27100 Pavia, Italy.
International Journal of Molecular Sciences
|October 16, 2024
Summary
4,4'-dihydroxy-trans-stilbene (DHS) and resveratrol (RSV) show potential against lung cancer. DHS notably reduced cancer cell proliferation, clonogenicity, and stemness features, suggesting its promise as an anticancer agent.
Area of Science:
- Oncology
- Pharmacology
- Biochemistry
Background:
- Lung cancer is a challenging tumor due to aggressive proliferation, metastasis, and cancer stem cells (CSCs).
- Natural compounds like resveratrol (RSV) are explored for cancer chemoprevention.
- 4,4'-dihydroxy-trans-stilbene (DHS), an RSV analogue, shows enhanced activity in preclinical models.
Purpose of the Study:
- To investigate the effects of DHS and RSV on A549 lung cancer cells.
- To analyze the impact of these stilbenes on cancer stem cell (CSC) features, focusing on the side population (SP) fraction.
Main Methods:
- Treatment of A549 lung cancer cells with DHS and RSV.
- Isolation of CSCs via side population (SP) sorting.
- Analysis of cell cycle progression, clonogenicity, soft agar colony formation, stemness marker expression, and spheroid formation.
Main Results:
- Both DHS and RSV inhibited cell cycle progression; DHS reduced the S phase, while RSV increased it.
- DHS treatment led to a 50% reduction in clonogenicity and soft agar colony formation.
- DHS and RSV decreased stemness marker expression in A549 cells and SP fraction.
- DHS significantly reduced spheroid formation and SOX2 levels in SP cells more than RSV.
Conclusions:
- Stilbenes, particularly DHS, impact stemness features in A549 lung cancer cells and their SP fraction.
- DHS demonstrates potent anticancer effects, including inhibition of proliferation and stemness.
- DHS shows potential as an anticancer agent, usable alone or in combination therapy for lung cancer.

