Different expression levels of glycans on leukemic cells-a novel screening method with molecularly imprinted polymers (MIP) targeting sialic acid

被引:37
作者
El-Schich, Zahra [1 ]
Abdullah, Mohammad [1 ]
Shinde, Sudhirkumar [1 ]
Dizeyi, Nishtman [2 ]
Rosen, Anders [3 ]
Sellergren, Borje [1 ]
Wingren, Anette Gjorloff [1 ]
机构
[1] Malmo Univ, Fac Hlth & Soc, Dept Biomed Sci, Malmo, Sweden
[2] Lund Univ, Dept Translat Med, Malmo, Sweden
[3] Linkoping Univ, Div Cell Biol, Dept Clin & Expt Med, Linkoping, Sweden
关键词
Chronic lymphocytic leukemia; Lectin; Molecular imprinting polymers; Sialic acid; L-SELECTIN; CANCER; METASTASIS; ANTIGEN; NANOPARTICLES; ACTIVATION; LEUKOCYTES; PHENOTYPE; CARCINOMA; RESIDUES;
D O I
10.1007/s13277-016-5280-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sialic acid (SA) is normally expressed on the cell membranes and is located at the terminal position of the sugar chains. SA plays an important role for regulation of the innate immunity, function as markers of the cells and can be recognized by a variety of receptors. Interestingly, the level of SA expression is increased on metastatic cancer cells. The availability of specific antibodies against SA is limited and, therefore, biomarker tools for detection of SA are lacking. We have recently presented a novel method for specific fluorescence labeling of SA molecular imprinted polymers (MIP). Here, we have performed an extended screening of SA expression by using SA-MIP and included four different chronic lymphocytic leukemia (CLL) cell lines, conveniently analyzed by flow cytometry and fluorescence microscopy. SA expression was detected in four cell lines at different levels, and the SA expression were verified with lectin-FITC. These results show that SA-MIP can be used as a plastic antibody for detection of SA using both flow cytometry and fluorescence microscopy. We suggest that SA-MIP can be used for screening of different tumor cells of various stages, including CLL cells.
引用
收藏
页码:13763 / 13768
页数:6
相关论文
共 31 条
[1]   Molecular imprinting science and technology: a survey of the literature for the years up to and including 2003 [J].
Alexander, C ;
Andersson, HS ;
Andersson, LI ;
Ansell, RJ ;
Kirsch, N ;
Nicholls, IA ;
O'Mahony, J ;
Whitcombe, MJ .
JOURNAL OF MOLECULAR RECOGNITION, 2006, 19 (02) :106-180
[2]   Synergistic effects of L- and P-selectin in facilitating tumor metastasis can involve non-mucin ligands and implicate leukocytes as enhancers of metastasis [J].
Borsig, L ;
Wong, R ;
Hynes, RO ;
Varki, NM ;
Varki, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (04) :2193-2198
[3]   Nanoparticles for improving cancer diagnosis [J].
Chen, Hongmin ;
Zhen, Zipeng ;
Todd, Trever ;
Chu, Paul K. ;
Xie, Jin .
MATERIALS SCIENCE & ENGINEERING R-REPORTS, 2013, 74 (03) :35-69
[4]   Lectin-Tagged Fluorescent Polymeric Nanoparticles for Targeting of Sialic Acid on Living Cells [J].
Cho, Jaebum ;
Kushiro, Keiichiro ;
Teramura, Yuji ;
Takai, Madoka .
BIOMACROMOLECULES, 2014, 15 (06) :2012-2018
[5]   Differential expression of the α2,3-sialic acid residues in breast cancer is associated with metastatic potential [J].
Cui, Hongxia ;
Lin, Yu ;
Yue, Liling ;
Zhao, Xuemei ;
Liu, Jicheng .
ONCOLOGY REPORTS, 2011, 25 (05) :1365-1371
[6]   The repertoire of glycan determinants in the human glycome [J].
Cummings, Richard D. .
MOLECULAR BIOSYSTEMS, 2009, 5 (10) :1087-1104
[7]   B-cell chronic lymphocytic leukemia cells express a surface membrane phenotype of activated, antigen-experienced B lymphocytes [J].
Damle, RN ;
Ghiotto, F ;
Valetto, A ;
Albasiano, E ;
Fais, F ;
Yan, XJ ;
Sison, CP ;
Allen, SL ;
Kolitz, J ;
Schulman, P ;
Vinciguerra, VP ;
Budde, P ;
Frey, J ;
Rai, KR ;
Ferrarini, M ;
Chiorazzi, N .
BLOOD, 2002, 99 (11) :4087-4093
[8]  
DENNIS JW, 1989, CANCER CELL-MON REV, V1, P87
[9]  
Dhabangi A, 2015, JAMA-J AM MED ASSOC, P1
[10]   Overexpression of tumour-associated carbohydrate antigen sialyl-Tn in advanced bladder tumours [J].
Ferreira, Jose Alexandre ;
Videira, Paula A. ;
Lima, Luis ;
Pereira, Sofia ;
Silva, Mariana ;
Carrascal, Mylene ;
Seuerino, Paulo F. ;
Fernandes, Elisabete ;
Almeida, Andreia ;
Costa, Ceu ;
Vitorino, Rui ;
Amaro, Teresina ;
Oliveira, Maria J. ;
Reis, Celso A. ;
Dall'Olio, Fabio ;
Amado, Francisco ;
Santos, Lucio Lara .
MOLECULAR ONCOLOGY, 2013, 7 (03) :719-731