Transmembrane mucins as novel therapeutic targets

被引:23
作者
Constantinou, Pamela E. [1 ]
Danysh, Brian P. [1 ]
Dharmaraj, Neeraja [1 ]
Carson, Daniel D. [1 ,2 ]
机构
[1] Rice Univ, Dept Biochem & Cell Biol, Houston, TX 77251 USA
[2] MD Anderson Canc Ctr, Dept Biochem & Mol Biol, Houston, TX 77030 USA
关键词
cytokines; MUC1; MUC16; MUC4; nanomedicine; steroid hormones;
D O I
10.1586/EEM.11.70
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Membrane-tethered mucin glycoproteins are abundantly expressed at the apical surfaces of simple epithelia, where they play important roles in lubricating and protecting tissues from pathogens and enzymatic attack. Notable examples of these mucins are MUC1, MUC4 and MUC16 (also known as cancer antigen 125). In adenocarcinomas, apical mucin restriction is lost and overall expression is often highly increased. High-level mucin expression protects tumors from killing by the host immune system, as well as by chemotherapeutic agents, and affords protection from apoptosis. Mucin expression can increase as the result of gene duplication and/ or in response to hormones, cytokines and growth factors prevalent in the tumor milieu. Rises in the normally low levels of mucin fragments in serum have been used as markers of disease, such as tumor burden, for many years. Currently, several approaches are being examined that target mucins for immunization or nanomedicine using mucin-specific antibodies.
引用
收藏
页码:835 / 848
页数:14
相关论文
共 183 条
  • [1] Cancer-associated MUC1 mucin inhibits human T-cell proliferation, which is reversible by IL-2
    Agrawal, B
    Krantz, MJ
    Reddish, MA
    Longenecker, BM
    [J]. NATURE MEDICINE, 1998, 4 (01) : 43 - 49
  • [2] Agrawal B, 1998, CANCER RES, V58, P4079
  • [3] CA 15-3 is predictive of response and disease recurrence following treatment in locally advanced breast cancer
    Al-Azawi, Dhafir
    Kelly, Gabrielle
    Myers, Eddie
    McDermott, Enda W.
    Hill, Arnold D. K.
    Duffy, Michael J.
    O Higgins, Niall
    [J]. BMC CANCER, 2006, 6 (1)
  • [4] Effect of pro-inflammatory mediators on membrane-associated mucins expressed by human ocular surface epithelial cells
    Albertsmeyer, Ann-Christin
    Kakkassery, Vinodh
    Spurr-Michaud, Sandra
    Beeks, Olivia
    Gipson, Ilene K.
    [J]. EXPERIMENTAL EYE RESEARCH, 2010, 90 (03) : 444 - 451
  • [5] IFN-γ-induced expression of MUC4 in pancreatic cancer cells is mediated by STAT-1 upregulation:: a novel mechanism for IFN-γ response
    Andrianifahanana, M.
    Singh, A. P.
    Nemos, C.
    Ponnusamy, M. P.
    Moniaux, N.
    Mehta, P. P.
    Varshney, G. C.
    Batra, S. K.
    [J]. ONCOGENE, 2007, 26 (51) : 7251 - 7261
  • [6] Synergistic induction of the MUC4 mucin gene by interferon-γ and retinoic acid in human pancreatic tumour cells involves a reprogramming of signalling pathways
    Andrianifahanana, M
    Agrawal, A
    Singh, AP
    Moniaux, N
    van Seuningen, I
    Aubert, JP
    Meza, J
    Batra, SK
    [J]. ONCOGENE, 2005, 24 (40) : 6143 - 6154
  • [7] MUC16 mucin is expressed by the human ocular surface epithelia and carries the H185 carbohydrate epitope
    Argüeso, P
    Spurr-Michaud, S
    Russo, CL
    Tisdale, A
    Gipson, IK
    [J]. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (06) : 2487 - 2495
  • [8] Membrane-bound mucins: the mechanistic basis for alterations in the growth and survival of cancer cells
    Bafna, S.
    Kaur, S.
    Batra, S. K.
    [J]. ONCOGENE, 2010, 29 (20) : 2893 - 2904
  • [9] MUC1 and the MUCs: A family of human mucins with impact in cancer biology
    Baldus, SE
    Engelmann, K
    Hanisch, FG
    [J]. CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES, 2004, 41 (02) : 189 - 231
  • [10] Baruch A, 1997, INT J CANCER, V71, P741