Mechanisms of antitumor and immune-enhancing activities of MUC1/sec, a secreted form of mucin-1

被引:7
作者
Ilkovitch, Dan [1 ]
Carrio, Roberto [1 ,2 ]
Lopez, Diana M. [1 ,2 ]
机构
[1] Univ Miami, Dept Microbiol & Immunol, Miller Sch Med, Miami, FL 33101 USA
[2] Univ Miami, Miller Sch Med, Sylvester Comprehens Canc Ctr, Miami, FL 33136 USA
基金
美国国家卫生研究院;
关键词
Mucins; MUC1 secreted form; Antitumor activity; Immune-enhancing peptide; CCL2; Urokinase plasminogen activator; STATs; Myeloid-derived suppressor cells; REGULATORY T-CELLS; COLONY-STIMULATING FACTOR; MYELOID SUPPRESSOR-CELLS; TUMOR-ASSOCIATED MACROPHAGES; INFLAMMATORY-BOWEL-DISEASE; IMMATURE DENDRITIC CELLS; SENTINEL LYMPH-NODE; PLASMINOGEN-ACTIVATOR; IN-VIVO; BREAST-CANCER;
D O I
10.1007/s12026-013-8451-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mucin 1 (MUC1) is a polymorphic type 1 transmembrane protein found on the apical surface of normal cells lining the lumen of ducts and glands. Mucins are thought to provide mucosal protection from environmental exposures and carcinogens. An altered form of the MUC1 glycoprotein, which is hypoglycosylated, is expressed in several types of human cancers. In our laboratory, we have found that transfection of a murine mammary tumor cell line with a human secreted isoform of MUC1 rendered these DA-3 cells (DA-3/sec) incapable of growing in intact BALB/c mice. In contrast, implantation of DA-3 cells transfected with the human transmembrane isoform of MUC1 (DA-3/TM), resulted in tumor formation and ultimately death of the animals, similar to the DA-3 parental line. Importantly, inoculation of the DA-3/sec cells in immunodeficient nude mice resulted in tumor formation, indicating that the MUC1/sec molecule's antitumor activity is immunologically controlled. In this review, we summarize the studies we have performed to elucidate possible mechanisms for the immune-mediated antitumor effect of MUC1/sec and/or a unique peptide present in this mucin. Understanding these mechanisms may provide new immunotherapeutic approaches that could be used to target different types of cancer.
引用
收藏
页码:70 / 80
页数:11
相关论文
empty
未找到相关数据