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Alcoholic Extract Targets Warburg Effect, Apoptosis and Cell Cycle Progression in Colorectal Cancer Cell Lines

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2025 Mar 13
PMID 40076837
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Abstract

Colorectal cancer (CRC) is the second deadliest cancer in the Western world. Increased body weight, a diet rich in red meat and alcohol, as well as a sedentary lifestyle, are all involved in sporadic CRC pathogenesis. Since current CRC therapies show several side effects, there is a need to find new and more effective therapeutic approaches, allowing conventional drug dosages and toxicity to be reduced. alcoholic extract was characterized by LC-MS and its effect investigated on a healthy colon mucosa cell line and on different colorectal cancer cell lines. Cell viability, apoptosis and cell cycle progression were evaluated through flow cytometry; energy production and glycolysis were investigated using Seahorse technology, while cancer markers were analyzed through Western blotting. The untargeted metabolomics analysis of alcoholic extract revealed glycosides of different polyphenols and glycosides of cucurbitane-type triterpenes. This extract showed a stronger impact on CRC cell line viability compared to healthy colon cells. In the E705 CRC cell line, it induced cell apoptosis and caused the downregulation of glycolysis, inhibiting cell proliferation. On the other hand, SW480 CRC cells treated with extract showed G/M cell cycle arrest. This work shows that extract can reduce glycolysis and promote cell cycle arrest in CRC cells, suggesting that could represent a novel player in the prevention and treatment of CRC.

References
1.
Uribe M, Marrocco I, Yarden Y . EGFR in Cancer: Signaling Mechanisms, Drugs, and Acquired Resistance. Cancers (Basel). 2021; 13(11). PMC: 8197917. DOI: 10.3390/cancers13112748. View

2.
Pearlman R, Frankel W, Swanson B, Zhao W, Yilmaz A, Miller K . Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer. JAMA Oncol. 2016; 3(4):464-471. PMC: 5564179. DOI: 10.1001/jamaoncol.2016.5194. View

3.
Thanikachalam K, Khan G . Colorectal Cancer and Nutrition. Nutrients. 2019; 11(1). PMC: 6357054. DOI: 10.3390/nu11010164. View

4.
McCullough M, Zoltick E, Weinstein S, Fedirko V, Wang M, Cook N . Circulating Vitamin D and Colorectal Cancer Risk: An International Pooling Project of 17 Cohorts. J Natl Cancer Inst. 2018; 111(2):158-169. PMC: 6376911. DOI: 10.1093/jnci/djy087. View

5.
Masci D, Puxeddu M, Silvestri R, La Regina G . Metabolic Rewiring in Cancer: Small Molecule Inhibitors in Colorectal Cancer Therapy. Molecules. 2024; 29(9). PMC: 11085455. DOI: 10.3390/molecules29092110. View