Glycophenotypic alterations induced by Pteridium aquilinum in mice gastric mucosa: synergistic effect with Helicobacter pylori infection

Autor: Steven R. Head, Ana Magalhães, Suzanne Papp, Joana Gomes, Valérie Michel, Celso A. Reis, Ana Sofia Carvalho, Gilberto E. Hernandez, Fátima Gärtner, Eliette Touati, Leonor David
Přispěvatelé: Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Universidade do Porto, The SCRIPPS Research Institute (SCRIPPS), University of California [Los Angeles] (UCLA), University of California-University of California, Pathogenèse de Helicobacter, Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS), This work was supported by Fundação para a Ciência e a Tecnologia – [FCT (PIC/IC/82716/2007), grant number SFRH/BD/40563/2007 to J.G and SFRH/BPD/75871/2011 to A.M.], and the Programa de Acções Universitárias Integradas Luso-Francesas - PAULIF [grant number LC/HS/ED/2010-308, F-TC04/11]. The resources and collaborative efforts provided by the Consortium for Functional Glycomics were funded by grant NIGMS-GM62116., Universidade do Porto = University of Porto, The Scripps Research Institute [La Jolla, San Diego], Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)
Jazyk: angličtina
Rok vydání: 2012
Předmět:
Bacterial Diseases
Mouse
MESH: Carbohydrate Metabolism
MESH: Helicobacter Infections/pathology
Glycobiology
Biochemistry
Transcriptome
Mice
0302 clinical medicine
[SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases
MESH: Gastric Mucosa/drug effects
MESH: Animals
Histochemistry
MESH: Helicobacter Infections/complications
0303 health sciences
Cocarcinogenesis
Multidisciplinary
biology
Enzyme Classes
Immunochemistry
Cancer Risk Factors
Environmental Causes of Cancer
Animal Models
Immunohistochemistry
MESH: Helicobacter pylori/isolation & purification
Enzymes
3. Good health
Infectious Diseases
Phenotype
medicine.anatomical_structure
Oncology
030220 oncology & carcinogenesis
Cytochemistry
Carbohydrate Metabolism
Medicine
medicine.symptom
Immunocytochemistry
C1GALT1
Research Article
MESH: Plant Extracts/toxicity
MESH: Pteridium/chemistry
Science
Carbohydrates
Inflammation
[SDV.CAN]Life Sciences [q-bio]/Cancer
MESH: Stomach Neoplasms/complications
MESH: Phenotype
Helicobacter Infections
Microbiology
03 medical and health sciences
Model Organisms
Stomach Neoplasms
MESH: Cocarcinogenesis
[SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry
Molecular Biology/Genomics [q-bio.GN]

Glycosyltransferase
Gastric mucosa
medicine
Animals
Biology
MESH: Mice
Carcinogen
MESH: Helicobacter Infections/microbiology
Glycoproteins
Pteridium
030304 developmental biology
Helicobacter pylori
Plant Extracts
Glycosyltransferases
MESH: Immunohistochemistry
biology.organism_classification
Gastric Mucosa
biology.protein
Pteridium aquilinum
MESH: Stomach Neoplasms/etiology
Zdroj: PLoS ONE
PLoS ONE, Public Library of Science, 2012, 7 (6), pp.e38353. ⟨10.1371/journal.pone.0038353⟩
PLoS ONE, Vol 7, Iss 6, p e38353 (2012)
PLoS ONE, 2012, 7 (6), pp.e38353. ⟨10.1371/journal.pone.0038353⟩
ISSN: 1932-6203
Popis: International audience; The bracken fern Pteridium aquilinum is a plant known to be carcinogenic to animals. Epidemiological studies have shown an association between bracken fern exposure and gastric cancer development in humans. The biological effects of exposure to this plant within the gastric carcinogenesis process are not fully understood. In the present work, effects in the gastric mucosa of mice treated with Pteridium aquilinum were evaluated, as well as molecular mechanisms underlying the synergistic role with Helicobacter pylori infection. Our results showed that exposure to Pteridium aquilinum induces histomorphological modifications including increased expression of acidic glycoconjugates in the gastric mucosa. The transcriptome analysis of gastric mucosa showed that upon exposure to Pteridium aquilinum several glycosyltransferase genes were differently expressed, including Galntl4, C1galt1 and St3gal2, that are mainly involved in the biosynthesis of simple mucin-type carbohydrate antigens. Concomitant treatment with Pteridium aquilinum and infection with Helicobacter pylori also resulted in differently expressed glycosyltransferase genes underlying the biosynthesis of terminal sialylated Lewis antigens, including Sialyl-Lewis x. These results disclose the molecular basis for the altered pattern of glycan structures observed in the mice gastric mucosa. The gene transcription alterations and the induced glycophenotypic changes observed in the gastric mucosa contribute for the understanding of the molecular mechanisms underlying the role of Pteridium aquilinum in the gastric carcinogenesis process.
Databáze: OpenAIRE