Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

As Australian lupin cultivars are rich sources of polyphenols, dietary fibers, high-quality proteins, and abundant bioactive compounds with significant antioxidant, antidiabetic, and anticancer activities, this research work is aimed at investigating the colon cancer alleviation activity of nine cultivars of lupin seeds on HCT116 and HT29 colon carcinoma cell lines through anti-proliferation assay, measurement of apoptosis, and identification of the mechanism of apoptosis. Nine cultivars were pre-screened for anti-proliferation of HCT116 and HT29 cells along with consideration of the impact of heat processing on cancer cell viability. Mandelup and Jurien showed significant inhibition of HCT116 cells, whereas the highest inhibition of HT29 cell proliferation was attained by Jurien and Mandelup. Processing decreased the anti-proliferation activity drastically. Lupin cultivars Mandelup, Barlock, and Jurien (dose: 300 μg/mL) induced early and late apoptosis of colon cancer cells in Annexin V-FITC assay. The mechanism of apoptosis was explored, which involves boosting of caspases-3/7 activation and intracellular reactive oxygen species (ROS) generation in HCT116 cells (Mandelup and Barlock) and HT29 cells (Jurien and Mandelup). Thus, the findings showed that lupin cultivars arrest cell cycles by inducing apoptosis of colorectal carcinoma cells triggered by elevated ROS generation and caspases-3/7 activation.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10647522PMC
http://dx.doi.org/10.3390/cells12212557DOI Listing

Publication Analysis

Top Keywords

caspases-3/7 activation
12
lupin cultivars
12
australian lupin
8
lupin seeds
8
reactive oxygen
8
oxygen species
8
generation caspases-3/7
8
colon cancer
8
hct116 ht29
8
mechanism apoptosis
8

Similar Publications

Anticancer Activity of Ethanolic Extract of in Breast Cancer Lines MCF-7 and MDA-MB-231.

Int J Mol Sci

August 2025

Ingeniería Bioquímica, Escuela Nacional de Ciencias Biológicas (ENCB)-Instituto Politécnico Nacional, Ciudad de México 07738, Mexico.

Breast cancer is a serious public health problem worldwide. Although current treatments with drugs such as cisplatin and paclitaxel are effective, they are associated with severe adverse effects and the development of drug resistance, which has prompted the search for new therapeutic strategies. In this context, the present study evaluated the anticancer activity of the ethanolic extract of (EET) on the breast cancer cell lines MCF-7 (hormone-sensitive) and MDA-MB-231 (triple-negative) using 2D and 3D models.

View Article and Find Full Text PDF

Allelopathy in phytoplankton species can modify the community structure by growth inhibition, organelle damage, cellular stress, metabolic modifications, and by inducing programmed cell death (PCD). In this study, the allelopathic responses of G. catenatum, a paralytic toxin harmful algal bloom (HAB) forming species, towards the raphidophyte C.

View Article and Find Full Text PDF

A novel non-nad-based PARP1 inhibitor, Japoflavone B, triggered Caspase-3/GSDME-mediated pyroptosis through ROS/p38/p53 pathway in NSCLC.

Chem Biol Interact

October 2025

Guangdong Key Laboratory of Regional Immunity and Diseases, Department of Pathogen Biology, Shenzhen University Medical School, Shenzhen, 518120, Guangdong Province, China; Center Lab of Longhua Branch and Department of Infectious Disease, Shenzhen People's Hospital (The Second Clinical Medical Coll

Pyroptosis has gotten more and more attention, in view of its link with innate immunity and disease. Most chemotherapy drugs could cause pyroptosis through caspase-3/GSDME pathway, which reshapes our understanding about the mechanism of anticancer. In our previous study, we found that a novel flavonoid, Japoflavone B (JFB), exhibited an excellent activity in vitro against the growth of cancer cells.

View Article and Find Full Text PDF

The Evaluation of Potential Anticancer Activity of Meloxicam-In Vitro Study on Amelanotic and Melanotic Melanoma.

Int J Mol Sci

June 2025

Department of Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences in Sosnowiec, Medical, University of Silesia in Katowice, Jagiellońska 4, 41-200 Sosnowiec, Poland.

Meloxicam (MLX), a member of the non-steroidal anti-inflammatory drugs (NSAIDs), is a preferential inhibitor of cyclooxygenase-2 (COX-2) responsible for the synthesis of pro-inflammatory prostaglandins. MLX, due to its inhibition of the COX-2 enzyme, which is overexpressed in many cancers, including melanoma, leading to rapid growth, angiogenesis, and metastasis, represents a potentially important compound with anticancer activity. This study aimed to investigate the potential anticancer activity of meloxicam against amelanotic C32 and melanotic COLO 829 melanoma cell lines.

View Article and Find Full Text PDF

Breast cancer is a disease with a high incidence and mortality rate worldwide. There is a growing interest in the search for alternative treatments with a good cytotoxic effect but fewer adverse effects, because paclitaxel and cis-platinum treatments present severe adverse effects. The aim of this study was evaluating the antitumor activity of ethyl acetate extract of Benth (EAB) in breast cancer cell lines.

View Article and Find Full Text PDF