Literature DB >> 25727146

Simple sugars to complex disease--mucin-type O-glycans in cancer.

Matthew R Kudelka1, Tongzhong Ju1, Jamie Heimburg-Molinaro1, Richard D Cummings2.   

Abstract

Mucin-type O-glycans are a class of glycans initiated with N-acetylgalactosamine (GalNAc) α-linked primarily to Ser/Thr residues within glycoproteins and often extended or branched by sugars or saccharides. Most secretory and membrane-bound proteins receive this modification, which is important in regulating many biological processes. Alterations in mucin-type O-glycans have been described across tumor types and include expression of relatively small-sized, truncated O-glycans and altered terminal structures, both of which are associated with patient prognosis. New discoveries in the identity and expression of tumor-associated O-glycans are providing new avenues for tumor detection and treatment. This chapter describes mucin-type O-glycan biosynthesis, altered mucin-type O-glycans in primary tumors, including mechanisms for structural changes and contributions to the tumor phenotype, and clinical approaches to detect and target altered O-glycans for cancer treatment and management.
© 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Blood group; Cancer; Carbohydrate; GalNAc; Glycan; Glycosylation; Golgi; Mucin; Tn; Tumor

Mesh:

Substances:

Year:  2015        PMID: 25727146      PMCID: PMC5812724          DOI: 10.1016/bs.acr.2014.11.002

Source DB:  PubMed          Journal:  Adv Cancer Res        ISSN: 0065-230X            Impact factor:   6.242


  319 in total

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Journal:  J Biol Chem       Date:  1999-02-19       Impact factor: 5.157

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7.  Regulation of cytokine receptors by Golgi N-glycan processing and endocytosis.

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8.  Immunohistochemical study of mucin carbohydrates and core proteins in human pancreatic tumors.

Authors:  M Osako; S Yonezawa; B Siddiki; J Huang; J J Ho; Y S Kim; E Sato
Journal:  Cancer       Date:  1993-04-01       Impact factor: 6.860

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6.  Specific N-Linked Glycosylation Patterns in Areas of Necrosis in Tumor Tissues.

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7.  Highly Sensitive O-Glycan Profiling for Human Serum Proteins Reveals Gender-Dependent Changes in Colorectal Cancer Patients.

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