Literature DB >> 26255117

Antiproliferative and pro-apoptotic effects of three fungal exocellular β-glucans in MCF-7 breast cancer cells is mediated by oxidative stress, AMP-activated protein kinase (AMPK) and the Forkhead transcription factor, FOXO3a.

Eveline A I F Queiroz1, Zuleica B Fortes2, Mário A A da Cunha3, Aneli M Barbosa4, Neelam Khaper5, Robert F H Dekker6.   

Abstract

Fungal β-d-glucans of the (1→3)-type are known to exhibit direct antitumor effects, and can also indirectly decrease tumor proliferation through immunomodulatory responses. The underlying molecular mechanisms involved in decreasing tumor formation, however, are not well understood. In this study, we examined the antiproliferative role and mechanism of action of three different fungal exocellular β-glucans in MCF-7 breast cancer cells. The β-glucans were obtained from Botryosphaeria rhodina MAMB-05 [two botryosphaerans; (1→3)(1→6)-β-d-glucan; one produced on glucose, the other on fructose] and Lasiodiplodia theobromae MMPI [lasiodiplodan; (1→6)-β-d-glucan, produced on glucose]. Using the cell proliferation-MTT assay, we showed that the β-glucans exhibited a time- and concentration-dependent antiproliferative activity (IC50, 100μg/ml). Markers of cell cycle, apoptosis, necrosis and oxidative stress were analyzed using flow cytometry, RT-PCR and Western blotting. Exposure to β-glucans increased apoptosis, necrosis, oxidative stress, mRNA expression of p53, p27 and Bax; the activity of AMP-activated protein-kinase, Forkhead transcription factor FOXO3a, Bax and caspase-3; and decreased the activity of p70S6K in MCF-7 cells. In the presence of hydrogen peroxide, the fungal β-glucans increased oxidative stress, which was associated with reduced cell viability. We showed that these β-glucans exhibited an antiproliferative effect that was associated with apoptosis, necrosis and oxidative stress. This study demonstrated for the first time that the apoptosis induced by β-glucans was mediated by AMP-activated protein-kinase and Forkhead transcription factor, FOXO3a. Our findings provide novel mechanistic insights into their antiproliferative roles, and compelling evidence that these β-glucans possess a broad range of biomodulatory properties that may prove useful in cancer treatment.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  AMPK; Apoptosis; Botryosphaeran; FOXO3a; Lasiodiplodan; Oxidative stress

Mesh:

Substances:

Year:  2015        PMID: 26255117     DOI: 10.1016/j.biocel.2015.08.003

Source DB:  PubMed          Journal:  Int J Biochem Cell Biol        ISSN: 1357-2725            Impact factor:   5.085


  11 in total

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Authors:  M R Ricciardi; R Licchetta; S Mirabilii; M Scarpari; A Parroni; A A Fabbri; P Cescutti; M Reverberi; C Fanelli; A Tafuri
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5.  Intracerebroventricular administration of the (1→6)-β-d-glucan (lasiodiplodan) in male rats prevents d-penicillamine-induced behavioral alterations and lipoperoxidation in the cortex.

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Authors:  Yuwan Zhao; Qiuming Luo; Jierong Mo; Jianwei Li; Dongcai Ye; Zhixian Ao; Lixin Chen; Jianjun Liu
Journal:  J Cancer       Date:  2020-03-31       Impact factor: 4.478

10.  Network Pharmacology/Metabolomics-Based Validation of AMPK and PI3K/AKT Signaling Pathway as a Central Role of Shengqi Fuzheng Injection Regulation of Mitochondrial Dysfunction in Cancer-Related Fatigue.

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Journal:  Oxid Med Cell Longev       Date:  2021-07-16       Impact factor: 6.543

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