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We are analyzing https://link.springer.com/article/10.1186/s12885-015-1032-4.

Title:
RETRACTED ARTICLE: Melatonin attenuates the TLR4-mediated inflammatory response through MyD88- and TRIF-dependent signaling pathways in an in vivo model of ovarian cancer | BMC Cancer
Description:
Toll-like receptors (TLRs) are effector molecules expressed on the surface of ovarian cancer (OC) cells, but the functions of the TLR2/TLR4 signaling pathways in these cells remain unclear. Melatonin (mel) acts as an anti-inflammatory factor and has been reported to modulate TLRs in some aggressive tumor cell types. Therefore, we investigated OC and the effect of long-term mel therapy on the signaling pathways mediated by TLR2 and TLR4 via myeloid differentiation factor 88 (MyD88) and toll-like receptor-associated activator of interferon (TRIF) in an ethanol-preferring rat model. To induce OC, the left ovary of animals either consuming 10% (v/v) ethanol or not was injected directly under the bursa with a single dose of 100 μg of 7,12-dimethylbenz(a)anthracene (DMBA) dissolved in 10 μL of sesame oil. The right ovaries were used as sham-surgery controls. After developing OC, half of the animals received i.p. injections of mel (200 μg/100 g b.w./day) for 60 days. Although mel therapy was unable to reduce TLR2 levels, it was able to suppress the OC-associated increase in the levels of the following proteins: TLR4, MyD88, nuclear factor kappa B (NFkB p65), inhibitor of NFkB alpha (IkBα), IkB kinase alpha (IKK-α), TNF receptor-associated factor 6 (TRAF6), TRIF, interferon regulatory factor 3 (IRF3), interferon β (IFN-β), tumor necrosis factor alpha (TNF-α), and interleukin (IL)-6. In addition, mel significantly attenuated the expression of IkBα, NFkB p65, TRIF and IRF-3, which are involved in TLR4-mediated signaling in OC during ethanol intake. Collectively, our results suggest that mel attenuates the TLR4-induced MyD88- and TRIF-dependent signaling pathways in ethanol-preferring rats with OC.
Website Age:
28 years and 1 months (reg. 1997-05-29).

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  • Science
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🌠 Phenomenal Traffic: 5M - 10M visitors per month


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Keywords {🔍}

mel, etoh, tlr, article, nfkb, pubmed, signaling, google, scholar, figure, ovarian, cas, cells, cancer, melatonin, therapy, expression, myd, trif, animals, pathway, levels, irf, tumor, factor, treatment, group, inflammatory, nuclear, intake, rats, ikbα, groups, ethanol, ikkα, traf, tnfα, tolllike, results, receptor, cytokines, protein, analysis, tlrmediated, serous, table, res, cell, reduced, pineal,

Topics {✒️}

laboratory-grade pine shavings polymer anti-mouse igg nfkb-regulated pro-inflammatory cytokines rabbit monoclonal anti-ikkα sep-pak vac c-18 long-term mel therapy tris-glycine-methanol buffer article download pdf rabbit polyclonal anti-myd88 avoid inter-assay variability long-term melatonin treatment rabbit polyclonal anti-trif tlr4-mediated signaling pathway rabbit polyclonal anti-tlr2 mouse monoclonal anti-tlr4 p-mapa immunotherapy potentiates n-terminal region termed tnf-α receptor i-independent myd88-independent signaling pathway myd88-dependent signaling pathway ethanol-induced oxidative stress melatonin inhibits lps-induced rabbit polyclonal anti-ikbα myd88-mediated signaling promotes tlr4-mediated inflammatory pathway tlr4/nf-jb system tlr2-mediated signaling pathway high-fat-fed rabbits tgf-b-activated kinase 1 trif-dependent signaling pathways tlr4-mediated inflammatory genes rabbit monoclonal anti-traf6 positively regulate tlr2/tlr4 chemically-induced rat model neuroendocrine/circadian melatonin signal rabbit monoclonal anti-irf3 chemokine-based gene therapy mel-treated groups maintained long-term therapy full size image human circulating cd4 + cells anti-cancer therapeutic drugs tlr4-mediated inflammatory response ethanol-preferring rat model tlr2/tlr4 signaling pathways ethanol-mediated inflammatory response nfkb p65/p50 complex mel differentially regulated long-term treatment adaptor inducing ifn-beta

Schema {🗺️}

WebPage:
      mainEntity:
         headline:RETRACTED ARTICLE: Melatonin attenuates the TLR4-mediated inflammatory response through MyD88- and TRIF-dependent signaling pathways in an in vivo model of ovarian cancer
         description:Toll-like receptors (TLRs) are effector molecules expressed on the surface of ovarian cancer (OC) cells, but the functions of the TLR2/TLR4 signaling pathways in these cells remain unclear. Melatonin (mel) acts as an anti-inflammatory factor and has been reported to modulate TLRs in some aggressive tumor cell types. Therefore, we investigated OC and the effect of long-term mel therapy on the signaling pathways mediated by TLR2 and TLR4 via myeloid differentiation factor 88 (MyD88) and toll-like receptor-associated activator of interferon (TRIF) in an ethanol-preferring rat model. To induce OC, the left ovary of animals either consuming 10% (v/v) ethanol or not was injected directly under the bursa with a single dose of 100 μg of 7,12-dimethylbenz(a)anthracene (DMBA) dissolved in 10 μL of sesame oil. The right ovaries were used as sham-surgery controls. After developing OC, half of the animals received i.p. injections of mel (200 μg/100 g b.w./day) for 60 days. Although mel therapy was unable to reduce TLR2 levels, it was able to suppress the OC-associated increase in the levels of the following proteins: TLR4, MyD88, nuclear factor kappa B (NFkB p65), inhibitor of NFkB alpha (IkBα), IkB kinase alpha (IKK-α), TNF receptor-associated factor 6 (TRAF6), TRIF, interferon regulatory factor 3 (IRF3), interferon β (IFN-β), tumor necrosis factor alpha (TNF-α), and interleukin (IL)-6. In addition, mel significantly attenuated the expression of IkBα, NFkB p65, TRIF and IRF-3, which are involved in TLR4-mediated signaling in OC during ethanol intake. Collectively, our results suggest that mel attenuates the TLR4-induced MyD88- and TRIF-dependent signaling pathways in ethanol-preferring rats with OC.
         datePublished:2015-02-06T00:00:00Z
         dateModified:2025-05-15T00:00:00Z
         pageStart:1
         pageEnd:13
         license:http://creativecommons.org/publicdomain/zero/1.0/
         sameAs:https://doi.org/10.1186/s12885-015-1032-4
         keywords:
            Ovarian cancer
            Melatonin
            Inflammation
            TLR4
            MyD88
            TRIF
            Cancer Research
            Oncology
            Surgical Oncology
            Health Promotion and Disease Prevention
            Biomedicine
            general
            Medicine/Public Health
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            issn:
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         author:
               name:Luiz Gustavo A Chuffa
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                        name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
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                        type:PostalAddress
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               name:Leonardo O Mendes
               affiliation:
                     name:Institute of Biosciences, UNESP – Universidade Estadual Paulista
                     address:
                        name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
                        type:PostalAddress
                     type:Organization
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               name:Fábio R Ferreira Seiva
               affiliation:
                     name:UENP - Campus Luiz Meneghel
                     address:
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                        name:Center for the Study of Venoms and Venomous Animals (CEVAP), UNESP - Univ Estadual Paulista, Botucatu, Brazil
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               name:Francisco Eduardo Martinez
               affiliation:
                     name:UFSCar – Universidade Federal de São Carlos
                     address:
                        name:Department of Morphology and Pathology, UFSCar – Universidade Federal de São Carlos, São Carlos, Brazil
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      headline:RETRACTED ARTICLE: Melatonin attenuates the TLR4-mediated inflammatory response through MyD88- and TRIF-dependent signaling pathways in an in vivo model of ovarian cancer
      description:Toll-like receptors (TLRs) are effector molecules expressed on the surface of ovarian cancer (OC) cells, but the functions of the TLR2/TLR4 signaling pathways in these cells remain unclear. Melatonin (mel) acts as an anti-inflammatory factor and has been reported to modulate TLRs in some aggressive tumor cell types. Therefore, we investigated OC and the effect of long-term mel therapy on the signaling pathways mediated by TLR2 and TLR4 via myeloid differentiation factor 88 (MyD88) and toll-like receptor-associated activator of interferon (TRIF) in an ethanol-preferring rat model. To induce OC, the left ovary of animals either consuming 10% (v/v) ethanol or not was injected directly under the bursa with a single dose of 100 μg of 7,12-dimethylbenz(a)anthracene (DMBA) dissolved in 10 μL of sesame oil. The right ovaries were used as sham-surgery controls. After developing OC, half of the animals received i.p. injections of mel (200 μg/100 g b.w./day) for 60 days. Although mel therapy was unable to reduce TLR2 levels, it was able to suppress the OC-associated increase in the levels of the following proteins: TLR4, MyD88, nuclear factor kappa B (NFkB p65), inhibitor of NFkB alpha (IkBα), IkB kinase alpha (IKK-α), TNF receptor-associated factor 6 (TRAF6), TRIF, interferon regulatory factor 3 (IRF3), interferon β (IFN-β), tumor necrosis factor alpha (TNF-α), and interleukin (IL)-6. In addition, mel significantly attenuated the expression of IkBα, NFkB p65, TRIF and IRF-3, which are involved in TLR4-mediated signaling in OC during ethanol intake. Collectively, our results suggest that mel attenuates the TLR4-induced MyD88- and TRIF-dependent signaling pathways in ethanol-preferring rats with OC.
      datePublished:2015-02-06T00:00:00Z
      dateModified:2025-05-15T00:00:00Z
      pageStart:1
      pageEnd:13
      license:http://creativecommons.org/publicdomain/zero/1.0/
      sameAs:https://doi.org/10.1186/s12885-015-1032-4
      keywords:
         Ovarian cancer
         Melatonin
         Inflammation
         TLR4
         MyD88
         TRIF
         Cancer Research
         Oncology
         Surgical Oncology
         Health Promotion and Disease Prevention
         Biomedicine
         general
         Medicine/Public Health
      image:
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs12885-015-1032-4/MediaObjects/12885_2015_1032_Fig1_HTML.gif
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      isPartOf:
         name:BMC Cancer
         issn:
            1471-2407
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         type:
            Periodical
            PublicationVolume
      publisher:
         name:BioMed Central
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Luiz Gustavo A Chuffa
            affiliation:
                  name:Institute of Biosciences, UNESP – Universidade Estadual Paulista
                  address:
                     name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
            name:Beatriz A Fioruci-Fontanelli
            affiliation:
                  name:Institute of Biosciences, UNESP – Universidade Estadual Paulista
                  address:
                     name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Leonardo O Mendes
            affiliation:
                  name:Institute of Biosciences, UNESP – Universidade Estadual Paulista
                  address:
                     name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Fábio R Ferreira Seiva
            affiliation:
                  name:UENP - Campus Luiz Meneghel
                  address:
                     name:Institute of Biology, State University of North of Parana, UENP - Campus Luiz Meneghel, Bandeirantes, Brazil
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Marcelo Martinez
            affiliation:
                  name:UFSCar – Universidade Federal de São Carlos
                  address:
                     name:Department of Morphology and Pathology, UFSCar – Universidade Federal de São Carlos, São Carlos, Brazil
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Wagner J Fávaro
            affiliation:
                  name:UNICAMP – Universidade de Campinas
                  address:
                     name:Department of Anatomy, Cell Biology and Physiology and Biophysics, UNICAMP – Universidade de Campinas, Campinas, Brazil
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Raquel F Domeniconi
            affiliation:
                  name:Institute of Biosciences, UNESP – Universidade Estadual Paulista
                  address:
                     name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Patrícia FF Pinheiro
            affiliation:
                  name:Institute of Biosciences, UNESP – Universidade Estadual Paulista
                  address:
                     name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Lucilene Delazari dos Santos
            affiliation:
                  name:Center for the Study of Venoms and Venomous Animals (CEVAP), UNESP - Univ Estadual Paulista
                  address:
                     name:Center for the Study of Venoms and Venomous Animals (CEVAP), UNESP - Univ Estadual Paulista, Botucatu, Brazil
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Francisco Eduardo Martinez
            affiliation:
                  name:UFSCar – Universidade Federal de São Carlos
                  address:
                     name:Department of Morphology and Pathology, UFSCar – Universidade Federal de São Carlos, São Carlos, Brazil
                     type:PostalAddress
                  type:Organization
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      name:Institute of Biosciences, UNESP – Universidade Estadual Paulista
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      name:Institute of Biosciences, UNESP – Universidade Estadual Paulista
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      name:Institute of Biosciences, UNESP – Universidade Estadual Paulista
      address:
         name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
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         name:Institute of Biology, State University of North of Parana, UENP - Campus Luiz Meneghel, Bandeirantes, Brazil
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Person:
      name:Luiz Gustavo A Chuffa
      affiliation:
            name:Institute of Biosciences, UNESP – Universidade Estadual Paulista
            address:
               name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Beatriz A Fioruci-Fontanelli
      affiliation:
            name:Institute of Biosciences, UNESP – Universidade Estadual Paulista
            address:
               name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
               type:PostalAddress
            type:Organization
      name:Leonardo O Mendes
      affiliation:
            name:Institute of Biosciences, UNESP – Universidade Estadual Paulista
            address:
               name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
               type:PostalAddress
            type:Organization
      name:Fábio R Ferreira Seiva
      affiliation:
            name:UENP - Campus Luiz Meneghel
            address:
               name:Institute of Biology, State University of North of Parana, UENP - Campus Luiz Meneghel, Bandeirantes, Brazil
               type:PostalAddress
            type:Organization
      name:Marcelo Martinez
      affiliation:
            name:UFSCar – Universidade Federal de São Carlos
            address:
               name:Department of Morphology and Pathology, UFSCar – Universidade Federal de São Carlos, São Carlos, Brazil
               type:PostalAddress
            type:Organization
      name:Wagner J Fávaro
      affiliation:
            name:UNICAMP – Universidade de Campinas
            address:
               name:Department of Anatomy, Cell Biology and Physiology and Biophysics, UNICAMP – Universidade de Campinas, Campinas, Brazil
               type:PostalAddress
            type:Organization
      name:Raquel F Domeniconi
      affiliation:
            name:Institute of Biosciences, UNESP – Universidade Estadual Paulista
            address:
               name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
               type:PostalAddress
            type:Organization
      name:Patrícia FF Pinheiro
      affiliation:
            name:Institute of Biosciences, UNESP – Universidade Estadual Paulista
            address:
               name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
               type:PostalAddress
            type:Organization
      name:Lucilene Delazari dos Santos
      affiliation:
            name:Center for the Study of Venoms and Venomous Animals (CEVAP), UNESP - Univ Estadual Paulista
            address:
               name:Center for the Study of Venoms and Venomous Animals (CEVAP), UNESP - Univ Estadual Paulista, Botucatu, Brazil
               type:PostalAddress
            type:Organization
      name:Francisco Eduardo Martinez
      affiliation:
            name:UFSCar – Universidade Federal de São Carlos
            address:
               name:Department of Morphology and Pathology, UFSCar – Universidade Federal de São Carlos, São Carlos, Brazil
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
      name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
      name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
      name:Institute of Biology, State University of North of Parana, UENP - Campus Luiz Meneghel, Bandeirantes, Brazil
      name:Department of Morphology and Pathology, UFSCar – Universidade Federal de São Carlos, São Carlos, Brazil
      name:Department of Anatomy, Cell Biology and Physiology and Biophysics, UNICAMP – Universidade de Campinas, Campinas, Brazil
      name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
      name:Department of Anatomy, Institute of Biosciences, UNESP – Universidade Estadual Paulista, Botucatu, Brazil
      name:Center for the Study of Venoms and Venomous Animals (CEVAP), UNESP - Univ Estadual Paulista, Botucatu, Brazil
      name:Department of Morphology and Pathology, UFSCar – Universidade Federal de São Carlos, São Carlos, Brazil

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