MUC1: a target molecule for cancer therapy.

Ravibhushan Singh, Dilip Bandyopadhyay

Protein Engineering and Biotherapy, Advanced Centre for Treatment Research and Education in Cancer (ACTREC), Tata Memorial Centre, Navi Mumbai, India.

Journal Article: Cancer biology & therapy (impact factor: 2.71). 05/2007; 6(4):481-6.

Abstract

MUC1 is a mucin family protein, overexpressed in more than 90% of breast cancers in an underglycosylated form, exposing the core peptides of the extracellular domain that act as a potential target for antibody-mediated therapy. The highly conserved repeats of 20 amino acids VNTR varies between 20 and 125 depending on the allele. Each tandem repeat contains five potential O-glycosylation sites that have been exploited in designing cancer therapeutics. The core peptides in the tandem repeated VNTR domain are masked in normal cells and become exposed in the cancer cells associated mucins. The characteristics of the MUCI epitopes constituted with the tandem repeats and the carbohydrates present on MUC1 induce immune responses that favor targeted immunotherapy. In addition, aberrant glycosylation also plays an important role in enhancing the internalization of MUC1 into the cytoplasm making MUC1 a very attractive cytoplasmic delivery system of drugs and other therapeutic agents. MUC1 being present on most of the cancers of glandular epithelial origin, appears as a potential target for therapeutic interventions in these cancers.

Source: PubMed

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Keywords

20 amino acids VNTR varies
 
allele
 
attractive cytoplasmic delivery system
 
breast cancers
 
cancer therapeutics
 
conserved
 
core peptides
 
extracellular domain
 
glandular epithelial origin
 
internalization
 
MUC1
 
MUC1 induce immune responses
 
MUCI epitopes constituted
 
mucin family protein
 
mucins
 
potential O-glycosylation sites
 
potential target
 
therapeutic agents
 
therapeutic interventions
 
underglycosylated form