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Cellular Toxicity of Nanogenomedicine in MCF-7 Cell Line: MTT assay
Published on: April 3, 2009
Marine Natural Compound (Neviotin A) Displays Anticancer Efficacy by Triggering Transcriptomic Alterations and Cell
Quaiser Saquib1, Stefan Schwaiger2, Mostafa Alilou2
1Chair for DNA Research, Zoology Department, College of Sciences, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
Abstract:
We investigated the anticancer mechanism of a chloroform extract of marine sponge (Haliclona fascigera) (sample C) in human breast adenocarcinoma (MCF-7) cells. Viability analysis using MTT and neutral red uptake (NRU) assays showed that sample C exposure decreased the proliferation of cells. Flow cytometric data exhibited reactive oxygen species (ROS), nitric oxide (NO), dysfunction of mitochondrial potential, and apoptosis in sample C-treated MCF-7 cells. A qPCR array of sample C-treated MCF-7 cells showed crosstalk between different pathways of apoptosis, especially BIRC5, BCL2L2, and TNFRSF1A genes. Immunofluorescence analysis affirmed the localization of p53, bax, bcl2, MAPKPK2, PARP-1, and caspase-3 proteins in exposed cells. Bioassay-guided fractionation of sample C revealed Neviotin A as the most active compound triggering maximum cell death in MCF-7, indicating its pharmacological potency for the development of a drug for the treatment of human breast cancer.
Insights
A marine sponge extract (sample C) from Haliclona fascigera demonstrated anticancer effects against human breast cancer cells. It induced cell death by triggering apoptosis and identified Neviotin A as a potent compound for drug development.
Area of Science:
- Marine Natural Products Chemistry
- Cancer Biology
- Pharmacology
Background:
- Marine sponges are a rich source of bioactive compounds with potential therapeutic applications.
- Breast cancer remains a leading cause of mortality, necessitating novel treatment strategies.
- Understanding the mechanisms of action of natural compounds is crucial for drug discovery.
Purpose of the Study:
- To investigate the anticancer mechanism of a marine sponge extract (Haliclona fascigera, sample C) in human breast adenocarcinoma (MCF-7) cells.
- To identify the specific molecular pathways and compounds responsible for the observed anticancer activity.
Main Methods:
- Cell viability assays (MTT, neutral red uptake) to assess proliferation.
- Flow cytometry to analyze reactive oxygen species (ROS), nitric oxide (NO), mitochondrial potential, and apoptosis.
- Quantitative PCR (qPCR) array and immunofluorescence to examine gene and protein expression related to apoptosis pathways.
Main Results:
- Sample C significantly decreased MCF-7 cell proliferation.
- Treatment induced ROS, NO production, mitochondrial dysfunction, and apoptosis.
- Key apoptosis-related genes (BIRC5, BCL2L2, TNFRSF1A) and proteins (p53, bax, bcl2, MAPKPK2, PARP-1, caspase-3) were modulated.
- Bioassay-guided fractionation identified Neviotin A as the most potent compound, inducing significant cell death.
Conclusions:
- The marine sponge extract Haliclona fascigera exhibits significant anticancer activity against breast cancer cells.
- The extract induces apoptosis through complex signaling pathways involving ROS, NO, and mitochondrial dysfunction.
- Neviotin A is a promising pharmacologically active compound from this extract for potential breast cancer drug development.
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