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CEACAMS 1, 5, and 6 in disease and cancer: interactions with pathogens.
Thomas, Jerin; Klebanov, Addison; John, Sahara; Miller, Larry S; Vegesna, Anil; Amdur, Richard L; Bhowmick, Krishanu; Mishra, Lopa.
Afiliación
  • Thomas J; Donald and Barbara Zucker School of Medicine, Hempstead, NY 11549, USA.
  • Klebanov A; The Institute for Bioelectronic Medicine, The Feinstein Institutes for Medical Research, Northwell Health, Manhassett, NY 11030, USA.
  • John S; The Institute for Bioelectronic Medicine, The Feinstein Institutes for Medical Research, Northwell Health, Manhassett, NY 11030, USA.
  • Miller LS; Department of Medicine, The Institute for Bioelectronic Medicine, The Feinstein Institutes for Medical Research, Division of Gastroenterology, Northwell Health, Manhassett, NY 11030, USA.
  • Vegesna A; The Institute for Bioelectronic Medicine, The Feinstein Institutes for Medical Research, Northwell Health, Manhassett, NY 11030, USA.
  • Amdur RL; Quantitative Intelligence Unit, The Institutes for Health Systems Science and Bioelectronic Medicine, The Feinstein Institutes for Medical Research, Northwell Health, Manhassett, NY 11030, USA.
  • Bhowmick K; The Institute for Bioelectronic Medicine, The Feinstein Institutes for Medical Research, Northwell Health, Manhassett, NY 11030, USA.
  • Mishra L; The Institute for Bioelectronic Medicine, The Feinstein Institutes for Medical Research, Northwell Health, Manhassett, NY 11030, USA.
Genes Cancer ; 14: 12-29, 2023.
Article en En | MEDLINE | ID: mdl-36741860
ABSTRACT
The CEA family comprises 18 genes and 11 pseudogenes located at chromosome 19q13.2 and is divided into two main groups cell surface anchored CEA-related cell adhesion molecules (CEACAMs) and the secreted pregnancy-specific glycoproteins (PSGs). CEACAMs are highly glycosylated cell surface anchored, intracellular, and intercellular signaling molecules with diverse functions, from cell differentiation and transformation to modulating immune responses associated with infection, inflammation, and cancer. In this review, we explore current knowledge surrounding CEACAM1, CEACAM5, and CEACAM6, highlight their pathological significance in the areas of cancer biology, immunology, and inflammatory disease, and describe the utility of murine models in exploring questions related to these proteins.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Genes Cancer Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Genes Cancer Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos