Evidence map›Paper›PMID 38704796›Full record

ArticleMolecular biology reports2024

Marine seaweed endophytic fungi-derived active metabolites promote reactive oxygen species-induced cell cycle arrest and apoptosis in human breast cancer cells.

Jeyamanikandan Venkatachalam, Veronica Shalini Jeyadoss, Kabilan Subash Chandra Bose, Raghunandhakumar Subramanian

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Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5 citing papers in PubMed.

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5 · Who and what money

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4 authors.

Jeyamanikandan VenkatachalamDepartment of Biotechnology, Jeppiaar Engineering College, Chennai, 600 119, Tamilnadu, India.
Veronica Shalini JeyadossDepartment of Biotechnology, Jeppiaar Engineering College, Chennai, 600 119, Tamilnadu, India. shalinijeyadoss@gmail.com.
Kabilan Subash Chandra BoseDepartment of Biotechnology, Anna University, Chennai, 600 025, Tamilnadu, India.
Raghunandhakumar SubramanianCancer and Stem cell Research Lab, Department of Pharmacology, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences (SIMATS), Chennai, 600 077, Tamilnadu, India. raghunandhakumar@gmail.com.

Funding

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6 · The paper itself

Abstract

backgroundEndophytic fungi have an abundant sources rich source of rich bioactive molecules with pivotal pharmacological properties. Several studies have found that endophytic fungi-derived bioactive secondary metabolites have antiproliferative, anti-oxidant, and anti-inflammatory properties, but the molecular mechanism by which they induce cell cycle arrest and apoptosis pathways is unknown. This study aimed to determine the molecular mechanism underlying the anticancer property of the endophytic fungi derived active secondary metabolites on human breast cancer cells.

methodsIn this study, we identified four endophytic fungi from marine seaweeds and partially screened its phytochemical properties by Chromatography-Mass Spectrometry (GC-MS) analysis. Moreover, the molecular mechanism underlying the anticancer property of these active secondary metabolites (FA, FB, FC and FE) on human breast cancer cells were examined on MCF-7 cells by TT assay, Apoptotic assay by Acridine orang/Ethidium Bromide (Dual Staining), DNA Fragmentation by DAPI Staining, reactive oxygen species (ROS) determination by DCFH-DA assay, Cell cycle analysis was conducted Flow cytometry and the apoptotic signalling pathway was evaluated by westernblot analysis. Doxorubicin was used as a positive control drug for this experiment.

resultsThe GC-MS analysis of ethyl acetate extract of endophytic fungi from the marine macro-algae revealed the different functional groups and bioactive secondary metabolites. From the library, we observed the FC (76%), FB (75%), FA (73%) and FE (71%) have high level of antioxidant activity which was assessed by DPPH scavenging assay. Further, we evaluated the cytotoxic potentials of these secondary metabolites on human breast cancer MCF-7 cells for 24 h and the IC

conclusionOur findings, revealed the anticancer potential of endophytic fungi from marine seaweed as a valuable source of bioactive compounds with anticancer properties and underscore the significance of exploring marine-derived endophytic fungi as a promising avenue for the development of novel anticancer agents. Further investigations are necessary to isolate and characterize specific bioactive compounds responsible for these effects and to validate their therapeutic potential in preclinical and clinical settings.

Indexed as

ApoptosisBreast NeoplasmsCell Cycle CheckpointsEndophytesReactive Oxygen SpeciesSeaweedAntineoplastic AgentsCell ProliferationFemaleFungiGas Chromatography-Mass SpectrometryHumansMCF-7 CellsAntineoplastic AgentsReactive Oxygen SpeciesApoptosisBreast CancerCytotoxicityEndophytic fungiSecondary metabolites

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.