Articles producció científicaMedicina i Cirurgia

Exogenous FABP4 increases breast cancer cell proliferation and activates the expression of fatty acid transport proteins

  • Identification data

    Identifier:  imarina:5129576
    Authors:  Guaita-Esteruelas, Sandra; Bosquet, Alba; Saavedra, Paula; Guma, Josep; Girona, Josefa; Lam, Eric W -F; Amillano, Kepa; Borras, Joan; Masana, Lluis
    Abstract:
    Adipose tissue plays an important role in tumor progression, because it provides nutrients and adipokines to proliferating cells. Fatty acid binding protein 4 (FABP4) is a key adipokine for fatty acid transport. In metabolic pathologies, plasma levels of FABP4 are increased. However, the role of this circulating protein is unknown. Recent studies have demonstrated that FABP4 might have a role in tumor progression, but the molecular mechanisms involved are still unclear. In this study, we analysed the role of eFABP4 (exogenous FABP4) in breast cancer progression. MCF-7 and MDA-MB-231 breast cancer cells did not express substantial levels of FABP4 protein, but intracellular FABP4 levels increased after eFABP4 incubation. Moreover, eFABP4 enhanced the proliferation of these breast cancer cells but did not have any effect on MCF-7 and MDA-MB-231 cell migration. Additionally, eFABP4 induced the AKT and MAPK signaling cascades in breast cancer cells, and the inhibition of these pathways reduced the eFBAP4-mediated cell proliferation. Interestingly, eFABP4 treatment in MCF-7 cells increased levels of the transcription factor FoxM1 and the fatty acid transport proteins CD36 and FABP5. In summary, we showed that eFABP4 plays a key role in tumor proliferation and activates the expression of fatty acid transport proteins in MCF-7 breast cancer cells. © 2016 Wiley Periodicals, Inc.
  • Others:

    Author, as appears in the article.: Guaita-Esteruelas, Sandra; Bosquet, Alba; Saavedra, Paula; Guma, Josep; Girona, Josefa; Lam, Eric W -F; Amillano, Kepa; Borras, Joan; Masana, Lluis
    Department: Medicina i Cirurgia; Ciències Mèdiques Bàsiques
    URV's Author/s: BORRAS BALADA, JOAN LLUÍS / BOSQUET AGUDO, ALBA / Girona Tell, Josefa / GUAITA ESTERUELAS, SANDRA / Masana Marín, Luis / SAAVEDRA GARCIA, PAULA
    Keywords: Signal transduction; Proto-oncogene proteins c-akt; Metabolic pathways; Mcf-7 cells; Map kinase signaling system; Lipid metabolism; Lipid chaperones; Humans; Female; Fatty acid-binding proteins; Fatty acid transport proteins; Fabp4 protein, human; Disease progression; Cell proliferation; Cell movement; Cell biology; Cancer progression; Breast neoplasms; Breast; lipid metabolism; lipid chaperones; cell biology; cancer progression
    Abstract: Adipose tissue plays an important role in tumor progression, because it provides nutrients and adipokines to proliferating cells. Fatty acid binding protein 4 (FABP4) is a key adipokine for fatty acid transport. In metabolic pathologies, plasma levels of FABP4 are increased. However, the role of this circulating protein is unknown. Recent studies have demonstrated that FABP4 might have a role in tumor progression, but the molecular mechanisms involved are still unclear. In this study, we analysed the role of eFABP4 (exogenous FABP4) in breast cancer progression. MCF-7 and MDA-MB-231 breast cancer cells did not express substantial levels of FABP4 protein, but intracellular FABP4 levels increased after eFABP4 incubation. Moreover, eFABP4 enhanced the proliferation of these breast cancer cells but did not have any effect on MCF-7 and MDA-MB-231 cell migration. Additionally, eFABP4 induced the AKT and MAPK signaling cascades in breast cancer cells, and the inhibition of these pathways reduced the eFBAP4-mediated cell proliferation. Interestingly, eFABP4 treatment in MCF-7 cells increased levels of the transcription factor FoxM1 and the fatty acid transport proteins CD36 and FABP5. In summary, we showed that eFABP4 plays a key role in tumor proliferation and activates the expression of fatty acid transport proteins in MCF-7 breast cancer cells. © 2016 Wiley Periodicals, Inc.
    Thematic Areas: Oncology; Molecular biology; Medicina veterinaria; Medicina ii; Medicina i; General medicine; Ciências biológicas iii; Ciências biológicas ii; Ciências biológicas i; Cancer research; Biotecnología; Biochemistry & molecular biology
    licence for use: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 08991987
    Author's mail: josefa.girona@urv.cat; josefa.girona@urv.cat; luis.masana@urv.cat
    Record's date: 2025-01-28
    Paper version: info:eu-repo/semantics/acceptedVersion
    Link to the original source: https://onlinelibrary.wiley.com/doi/abs/10.1002/mc.22485
    Licence document URL: https://repositori.urv.cat/ca/proteccio-de-dades/
    Paper original source: Molecular Carcinogenesis. 56 (1): 208-217
    APA: Guaita-Esteruelas, Sandra; Bosquet, Alba; Saavedra, Paula; Guma, Josep; Girona, Josefa; Lam, Eric W -F; Amillano, Kepa; Borras, Joan; Masana, Lluis (2017). Exogenous FABP4 increases breast cancer cell proliferation and activates the expression of fatty acid transport proteins. Molecular Carcinogenesis, 56(1), 208-217. DOI: 10.1002/mc.22485
    Article's DOI: 10.1002/mc.22485
    Entity: Universitat Rovira i Virgili
    Journal publication year: 2017
    Publication Type: Journal Publications
  • Keywords:

    Biochemistry & Molecular Biology,Cancer Research,Molecular Biology,Oncology
    Signal transduction
    Proto-oncogene proteins c-akt
    Metabolic pathways
    Mcf-7 cells
    Map kinase signaling system
    Lipid metabolism
    Lipid chaperones
    Humans
    Female
    Fatty acid-binding proteins
    Fatty acid transport proteins
    Fabp4 protein, human
    Disease progression
    Cell proliferation
    Cell movement
    Cell biology
    Cancer progression
    Breast neoplasms
    Breast
    lipid metabolism
    lipid chaperones
    cell biology
    cancer progression
    Oncology
    Molecular biology
    Medicina veterinaria
    Medicina ii
    Medicina i
    General medicine
    Ciências biológicas iii
    Ciências biológicas ii
    Ciências biológicas i
    Cancer research
    Biotecnología
    Biochemistry & molecular biology
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