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Article 2025 · 1 citations

<i>Tilia</i> species (linden) exert anti-cancer effects on MIA PaCa-2 cells through the modulation of oxidative stress and inflammation

Yuksel, Gamze, Ozhan, Yagmur, Guresci, Dilara, Guezelmeric, Etil, Sen, Nisa Beril, Bedir, Ipek, Senol, Onur, Emre, Gizem, Telci, Dilek, Petrikaite, Vilma, Sipahi, Hande

Abstract

This study investigated the anti-cancer effects of the chemically characterized Tilia species (linden) on MIA PaCa-2 cells by analyzing various cancer-triggering mechanisms, including oxidative stress and inflammation status. Extracts from the flowers, bracts, and inflorescences of T. cordata, T. platyphyllos, T. rubra, and T. tomentosa were evaluated for antioxidant activity; subsequently, their ability to mitigate inflammation was assessed through in vitro nitrite assays in LPS-induced RAW264.7 cells. The anticancer potentials of the extracts against MIA PaCa-2 pancreatic cancer cells were investigated in 2D (cytotoxic effect) and 3D (effect on spheroid growth) models in vitro. All investigated Tilia species displayed remarkable antioxidant activity and significantly inhibited LPS-induced nitrite, IL-6, and PGE2 production. Extract from T. rubra bracts showed the highest cytotoxic activity against MIA PaCa-2 cells with an IC50 value of 0.16 mg/mL, as well as the most significant delay on spheroid growth, which was further confirmed through the arrest in cell cycle. In the Annexin V cell death assays of T. rubra, cells treated with the flower extract exhibited the highest rate of necrotic population with 66.53%. Overall, our results highlight a potential use for Tilia extracts, particularly T. rubra, in pancreatic cancer treatment by modulating cell death.

Keywords
<italic>Tilia</italic> species Phenolic profile Antioxidant activity Anti-inflammatory activity Anticancer activity 3D spheroid model ANTIOXIDANT CANCER ASSAYS FLOS
WoS Categories
Multidisciplinary Sciences
Sustainable Development Goals
Citation
Journal
SCIENTIFIC REPORTS
Year
2025
Volume
15
Issue
1
ISSN
2045-2322
DOI
10.1038/s41598-025-86457-2
WoS UID
WOS:001401996200003
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