The biochemical utility of chromogranin A, chromogranin B and cocaine- and amphetamine-regulated transcript for neuroendocrine neoplasia.

Neuroendocrine neoplasia (NEN) is a heterogeneous group of tumours and often represents a therapeutic challenge to clinicians. The peptides chromogranin A (CgA), chromogranin B (CgB) and cocaine- and amphetamine-regulated transcript (CART) are widely distributed throughout the neuroendocrine system....

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Publicado en:Annals of Clinical Biochemistry Vol. 51; no. 1; pp. 8 - 22
Autores principales: Bech, P R, Martin, N M, Ramachandran, R, Bloom, S R
Formato: Journal Article
Publicado: Sage Publications Inc. Jan2014
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jan2014
      vid: 51
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      pub: Sage Publications Inc.
      place: Thousand Oaks, California
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        atl: The biochemical utility of chromogranin A, chromogranin B and cocaine- and amphetamine-regulated transcript for neuroendocrine neoplasia.
      aug:
        au:
          Bech, P R
          Martin, N M
          Ramachandran, R
          Bloom, S R
        affil: Division of Diabetes, Endocrinology and Metabolism, Imperial College London, London, UK.
      sug:
        subj:
          Protein Precursors
          Nerve Tissue Proteins
          Neuroendocrine Tumors
          Neuroendocrine Tumors Diagnosis
          Neuroendocrine Tumors Pathology
          Pancreas Metabolism
          Pancreas Pathology
          Prognosis
          Somatostatin Metabolism
          Tumor Markers, Biological
      ab: Neuroendocrine neoplasia (NEN) is a heterogeneous group of tumours and often represents a therapeutic challenge to clinicians. The peptides chromogranin A (CgA), chromogranin B (CgB) and cocaine- and amphetamine-regulated transcript (CART) are widely distributed throughout the neuroendocrine system. CgA and CgB have been used as general NEN biomarkers for many years, while CART has only recently been identified. Of these biomarkers, CgA is the most commonly used. However, circulating CgA concentrations exhibit considerable intra-individual biological variation, are altered by proton pump inhibitors (PPIs) and somatostatin analogues and are elevated in non-NEN malignancies. Therefore, interpretation of CgA results must be in the context of these confounding factors. The effects of treatment and non-NEN conditions on circulating CgB and CART concentrations are less well understood. CgB is less affected by impaired renal function and PPIs than CgA; while, circulating CART concentrations lack a diurnal variation in humans and are more reliable markers of pancreatic NEN malignancy than CgA. The utility of circulating CgA measurements in NEN prognosis, surveillance and disease recurrence has been widely investigated. However, the utility of CgB and CART in NEN management is yet to be elucidated. Further studies are needed to establish whether CgB and CART are useful alternatives to CgA.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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