Selective cytotoxicity of Arctium extracts in pancreatic, bladder, and colorectal cancer cell lines: A comparative dose-response study

Gastrointestinal and urinary tract cancers, including colorectal, pancreatic, and bladder malignancies, represent a major global health burden due to their high mortality and therapeutic resistance. In light of the limitations of current treatment strategies, plant-derived compounds with multitargeted actions have emerged as promising alternatives. This study aimed to evaluate the cytotoxic effects of methanol and dichloromethane:methanol (1:1) extracts of Arctium minus subsp. pubens, A. minus subsp. minus, and A. tomentosum var. glabrum on three human cancer cell lines: HTB-9 (bladder), DLD-1 (colorectal), and PANC-1 (pancreatic). Extracts were prepared from aerial parts of plants using two solvents of differing polarity. Cell viability was determined after 24 and 48 hours using the WST-1 assay. IC₅₀ values were calculated, and statistical comparisons were performed. All extracts exhibited dose-dependent cytotoxicity. The methanol extract of A. tomentosum showed the strongest effect in HTB-9 cells, while A. minus subsp. pubens demonstrated potent activity against DLD-1 and PANC-1 cells. The findings highlight the selective cytotoxic potential of Arctium species, especially A. minus subsp. pubens and A. tomentosum, which may serve as valuable candidates for further phytochemical and mechanistic anticancer studies.

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Publication Details

Journal
International Journal of Secondary Metabolite
Published
2026-03-09
DOI
https://doi.org/10.21448/ijsm.1702826
Primary Topic
Plant-derived Lignans Synthesis and Bioactivity
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article
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article

Selective cytotoxicity of Arctium extracts in pancreatic, bladder, and colorectal cancer cell lines: A comparative dose-response study

Ahmet Çakır, Beyza Ecem ÖZ BEDİR, Emine Terzi, Tuba Aydın et al.
International Journal of Secondary Metabolite
Plant-derived Lignans Synthesis and Bioactivity
article

Selective cytotoxicity of Arctium extracts in pancreatic, bladder, and colorectal cancer cell lines: A comparative dose-response study

Ahmet Çakır, Beyza Ecem ÖZ BEDİR, Emine Terzi, Tuba Aydın, Benan Kalaycı, Tuba Ozdemir Sancı, Fevzi Özgökçe
article en

Abstract

Gastrointestinal and urinary tract cancers, including colorectal, pancreatic, and bladder malignancies, represent a major global health burden due to their high mortality and therapeutic resistance. In light of the limitations of current treatment strategies, plant-derived compounds with multitargeted actions have emerged as promising alternatives. This study aimed to evaluate the cytotoxic effects of methanol and dichloromethane:methanol (1:1) extracts of Arctium minus subsp. pubens, A. minus subsp. minus, and A. tomentosum var. glabrum on three human cancer cell lines: HTB-9 (bladder), DLD-1 (colorectal), and PANC-1 (pancreatic). Extracts were prepared from aerial parts of plants using two solvents of differing polarity. Cell viability was determined after 24 and 48 hours using the WST-1 assay. IC₅₀ values were calculated, and statistical comparisons were performed. All extracts exhibited dose-dependent cytotoxicity. The methanol extract of A. tomentosum showed the strongest effect in HTB-9 cells, while A. minus subsp. pubens demonstrated potent activity against DLD-1 and PANC-1 cells. The findings highlight the selective cytotoxic potential of Arctium species, especially A. minus subsp. pubens and A. tomentosum, which may serve as valuable candidates for further phytochemical and mechanistic anticancer studies.

International Journal of Secondary Metabolite(Advanced Online Publication)
Van Yüzüncü Yıl Üniversitesi (TR), Ağrı İbrahim Çeçen University (TR), Ankara Yıldırım Beyazıt University (TR), Kilis 7 Aralık University (TR)
Good health and well-being
Openalex Percentile: Top 28%
Plant-derived Lignans Synthesis and Bioactivity
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Selective cytotoxicity of Arctium extracts in pancreatic, bladder, and colorectal cancer cell lines: A comparative dose-response study — Ahmet Çakır, Beyza Ecem ÖZ BEDİR, et al. · International Journal of Secondary Metabolite (2026) | TGRS Research Map | TGRS