Garambullo (Myrtillocactus geometrizans) reduces cell viability via apoptosis and inhibits colony formation in HT-29 and SW480 colon cancer cell lines.
{"title":"Garambullo (Myrtillocactus geometrizans) reduces cell viability via apoptosis and inhibits colony formation in HT-29 and SW480 colon cancer cell lines.","authors":"López-Alvarez Guadalupe Soledad, Gutierrez-Silerio Gloria Yareli, García-Solís Pablo, Morales-Bárcenas Rocio, Sánchez-Pérez Yesennia, Hernández-Puga Ana Gabriela, Vergara-Castañeda Haydé Azeneth","doi":"10.38212/2224-6614.3599","DOIUrl":null,"url":null,"abstract":"<p><p>Garambullo (Myrtillocactus geometrizans) is a Mexican wild fruit rich in phytochemicals. In this study, freeze-dried garambullo was subjected to in vitro gastrointestinal digestion and fermentation. The resulting fermented extract of garambullo (FEG) was evaluated for its effects on cell viability in HT-29 and SW480 CRC cell lines using MTT assays. After 24 h of treatment, FEG exhibited IC<sub>50</sub> values of 2985 μg/mL and 3200 μg/mL in HT-29 and SW480 cells, respectively, indicating a significant reduction in cell viability compared to the control group. This reduction was further confirmed by flow cytometry, which revealed increased late apoptosis and necrosis in HT-29 cells, and a pronounced increase of necrosis in SW480 cells treated with FEG. Molecular docking simulations further supported these findings, demonstrating that butyric acid, a metabolite identified in FEG, demonstrates energetically favorable interactions with Caspase-3 (ΔG: -5.41 kcal/mol) and RIPK1 (ΔG: -5.18 kcal/mol), suggesting potential multi-pathway involvement in apoptotic and necrosis-associated cell death. Furthermore, the colony-forming ability of these CRC cell lines was assessed using 3D culture assays. After 14 days, FEG reduced colony formation in SW480 cells, with complete suppression observed at 149 μg/mL. Notably, HT-29 cells exhibited greater sensitivity, as no colonies were detected at any of the tested concentrations (≥37 μg/mL). These findings indicate that FEG exerts significant anti-proliferative, proapoptotic, and anti-clonogenic effects in CRC cell lines, supporting its potential as a candidate for further investigation in therapeutic or preventive strategies.</p>","PeriodicalId":358,"journal":{"name":"Journal of Food and Drug Analysis","volume":"34 3","pages":"331-343"},"PeriodicalIF":3.3000,"publicationDate":"2026-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13592839/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Food and Drug Analysis","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.38212/2224-6614.3599","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"FOOD SCIENCE & TECHNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Garambullo (Myrtillocactus geometrizans) is a Mexican wild fruit rich in phytochemicals. In this study, freeze-dried garambullo was subjected to in vitro gastrointestinal digestion and fermentation. The resulting fermented extract of garambullo (FEG) was evaluated for its effects on cell viability in HT-29 and SW480 CRC cell lines using MTT assays. After 24 h of treatment, FEG exhibited IC50 values of 2985 μg/mL and 3200 μg/mL in HT-29 and SW480 cells, respectively, indicating a significant reduction in cell viability compared to the control group. This reduction was further confirmed by flow cytometry, which revealed increased late apoptosis and necrosis in HT-29 cells, and a pronounced increase of necrosis in SW480 cells treated with FEG. Molecular docking simulations further supported these findings, demonstrating that butyric acid, a metabolite identified in FEG, demonstrates energetically favorable interactions with Caspase-3 (ΔG: -5.41 kcal/mol) and RIPK1 (ΔG: -5.18 kcal/mol), suggesting potential multi-pathway involvement in apoptotic and necrosis-associated cell death. Furthermore, the colony-forming ability of these CRC cell lines was assessed using 3D culture assays. After 14 days, FEG reduced colony formation in SW480 cells, with complete suppression observed at 149 μg/mL. Notably, HT-29 cells exhibited greater sensitivity, as no colonies were detected at any of the tested concentrations (≥37 μg/mL). These findings indicate that FEG exerts significant anti-proliferative, proapoptotic, and anti-clonogenic effects in CRC cell lines, supporting its potential as a candidate for further investigation in therapeutic or preventive strategies.
期刊介绍:
The journal aims to provide an international platform for scientists, researchers and academicians to promote, share and discuss new findings, current issues, and developments in the different areas of food and drug analysis.
The scope of the Journal includes analytical methodologies and biological activities in relation to food, drugs, cosmetics and traditional Chinese medicine, as well as related disciplines of topical interest to public health professionals.