Apoptotic and Anti-Proliferative Potential of Spirulina platensis Methanolic Extract Against the Human Breast Cancer Cell Line MDA-MB-231: A Step Towards Functional Cancer Therapy.
1/5 보강
[INTRODUCTION] Algae have garnered increasing interest in the fields of medicine and nutrition as a source of nutritious and non-toxic healthcare supplements.
APA
Srivastava A, Siddiqi Z, et al. (2026). Apoptotic and Anti-Proliferative Potential of Spirulina platensis Methanolic Extract Against the Human Breast Cancer Cell Line MDA-MB-231: A Step Towards Functional Cancer Therapy.. Anti-cancer agents in medicinal chemistry. https://doi.org/10.2174/0118715206383642251105064036
MLA
Srivastava A, et al.. "Apoptotic and Anti-Proliferative Potential of Spirulina platensis Methanolic Extract Against the Human Breast Cancer Cell Line MDA-MB-231: A Step Towards Functional Cancer Therapy.." Anti-cancer agents in medicinal chemistry, 2026.
PMID
41833021 ↗
Abstract 한글 요약
[INTRODUCTION] Algae have garnered increasing interest in the fields of medicine and nutrition as a source of nutritious and non-toxic healthcare supplements. Spirulina platensis (SP), a microalga and a welldocumented nutritional supplement, is recognized for its high medicinal value and potential anticancer properties. The present study evaluated the apoptosis-inducing effect of methanolic extract of Spirulina platensis (SPM) on human breast cancer MDA-MB-231 cells.
[METHODS] The extract was prepared using standard methanol extraction techniques. Cytotoxicity was assessed using the MTT assay over varying concentrations and time intervals. Morphological changes were observed under a phase-contrast microscope. Apoptosis was further confirmed through acridine orange/ ethidium bromide (AO/EB) dual staining and DNA fragmentation analysis. The effect of SPM on normal HEK-293 cells was also evaluated to determine its selectivity and safety profile.
[RESULTS] HPLC analysis identified C-phycocyanin (C-PC) as the major bioactive phytoconstituent in the SPM extract. The extract showed antioxidant activity and dose- and time-dependent growth inhibition of MDA-MB-231 cells (IC50: 3433 μg/mL). Treated cells displayed apoptotic morphology under a phasecontrast microscope and late apoptosis at higher doses, confirmed by AO/EB staining. DNA fragmentation was observed in MDA-MB-231 cells but not in HEK-293 cells, which showed minimal cytotoxicity (IC₂⁽: 7250 μg/mL).
[DISCUSSION] The presence of C-PC most likely contributes to the extract's antioxidant and anticancer effects. SPM selectively induced apoptosis and inhibited proliferation in MDA-MB-231 cells, with a negligible impact on normal cells, highlighting its potential as a safe and natural anticancer candidate.
[CONCLUSION] As evident from the results, SPM extract has demonstrated potential for its clinical applications in cancer therapy as an adjunct to the main line of treatment, provided that further studies are carried out on other cancer cell lines and animal models in future.
[METHODS] The extract was prepared using standard methanol extraction techniques. Cytotoxicity was assessed using the MTT assay over varying concentrations and time intervals. Morphological changes were observed under a phase-contrast microscope. Apoptosis was further confirmed through acridine orange/ ethidium bromide (AO/EB) dual staining and DNA fragmentation analysis. The effect of SPM on normal HEK-293 cells was also evaluated to determine its selectivity and safety profile.
[RESULTS] HPLC analysis identified C-phycocyanin (C-PC) as the major bioactive phytoconstituent in the SPM extract. The extract showed antioxidant activity and dose- and time-dependent growth inhibition of MDA-MB-231 cells (IC50: 3433 μg/mL). Treated cells displayed apoptotic morphology under a phasecontrast microscope and late apoptosis at higher doses, confirmed by AO/EB staining. DNA fragmentation was observed in MDA-MB-231 cells but not in HEK-293 cells, which showed minimal cytotoxicity (IC₂⁽: 7250 μg/mL).
[DISCUSSION] The presence of C-PC most likely contributes to the extract's antioxidant and anticancer effects. SPM selectively induced apoptosis and inhibited proliferation in MDA-MB-231 cells, with a negligible impact on normal cells, highlighting its potential as a safe and natural anticancer candidate.
[CONCLUSION] As evident from the results, SPM extract has demonstrated potential for its clinical applications in cancer therapy as an adjunct to the main line of treatment, provided that further studies are carried out on other cancer cell lines and animal models in future.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
같은 제1저자의 인용 많은 논문 (5)
- Multifaceted role of RSPO2: Epigenetics, immunoregulatory, and therapeutic insights in colorectal cancer.
- Apoptosis Induction, Disruption of Cytoskeleton Remodeling and EMT Inhibition as Major Mechanism(s) Underlying the Pleiotropic Action of Withania somnifera in Breast Cancer.
- Prioritization of predisposition genes for familial non-medullary thyroid cancer by whole-genome sequencing.
- Hierarchical clustering defines hypermethylated RSPO2 as early-stage potential biomarker in colorectal cancer.
- Impact of Multidisciplinary Team Care on Patient-Reported Outcomes in Patients with Lung Cancer: A Systematic Review.
🏷️ 같은 키워드 · 무료전문 — 이 논문 MeSH/keyword 기반
- Cell Line-Dependent Cell Death Pathways Induced by Thymoquinone in Colorectal Cancer Cells.
- Thapsigargin enhanced chemotherapeutic sensitivity of irinotecan in the inflammation-induced colorectal cancer model in mice.
- Diagnostic and Prognostic Value of cfDNA Concentration and Fragmentation in Prostate Cancer.
- Probiotic WB4404 and WB4503 from Kimchi Induce Apoptosis in Human Colorectal Cancer Cells .
- Fragmenting the future with FLARE: a comprehensive fragmentomics pipeline based on long-read nanopore sequencing.
- Fisetin limits Chikungunya virus-induced apoptosis hallmarks in hepatocellular carcinoma cells.