Molecular imprinting of glycoproteins: From preparation to cancer theranostics

被引:28
作者
Ali, Muhammad Mujahid [1 ,2 ]
Zhu, Shoujun [1 ]
Amin, Farrukh Raza [3 ]
Hussain, Dilshad [4 ]
Du, Zhenxia [5 ]
Hu, Lianghai [1 ]
机构
[1] Jilin Univ, Ctr Supramol Chem Biol, Sch Life Sci, State Key Lab Supramol Struct & Mat, Changchun 130023, Peoples R China
[2] Southeast Univ, Natl Demonstrat Ctr Expt Biomed Engn Educ, State Key Lab Bioelect, Nanjing 210096, Peoples R China
[3] COMSATS Univ Islamabad, Ctr Climate Res & Dev, Pk Rd, Islamabad 45550, Pakistan
[4] Univ Karachi, Int Ctr Chem & Biol Sci, HEJ Res Inst Chem, Karachi 75270, Pakistan
[5] Beijing Univ Chem Technol, Coll Chem, Beijing Key Lab Environmentally Harmful Chem Anal, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
Molecularly imprinting; Glycoproteins; Biosensing; Cancer theranostics; Proteomics; IMMUNE-CHECKPOINT BLOCKADE; CIRCULATING TUMOR-CELLS; AFFINITY SANDWICH ASSAY; TARGETED DRUG-DELIVERY; SENSITIVE DETECTION; MESOPOROUS SILICA; GRAPHENE OXIDE; QUANTUM DOTS; HUMAN-BREAST; CARBON DOTS;
D O I
10.7150/thno.69189
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Glycoprotein imprinted polymers have rapidly grown as excellent receptors for cancer targeting, diagnostics, inhibition, and nanomedicines as they specifically target glycans and glycosites overexpressed in various tumors. Compared to natural antibodies, they are easy to synthesize, stable, and cost-efficient. Currently, no study specifically discusses glycoproteins imprinting strategies for cancer theranostics. In this review, firstly we explored various factors involved in designing and synthesis of glycoprotein imprinted materials, including, the characteristics and choice of monomers for imprinting, types of templates and their interactions involved, and the imprinting methods. Secondly, the integration of these MIPs with different probes that have been applied for in vitro and in vivo targeting for cancer diagnostics including biosensing and bioimaging, and image-guided therapeutic applications as nanomedicines. These Glycoprotein imprinted polymers have been found to specifically target the glycoprotein biomarkers and glycosylated cell receptors overexpressed in different cancers and have been reported as excellent diagnostic tools. As nanomedicines, they have been potentially employed in various modes of cancer therapy such as targeted drug delivery, photodynamic therapy, photothermal therapy, and nanoMIPs themselves as therapeutics for locally killing tumor cells. Although the research is still in its early stages and no real-world clinical trials on humans have been conducted, nanoMIPs have a promising future in this field. We believe these findings will pave the way for MIPs in advanced diagnostics, antibody treatment, and immunotherapy as future nanomedicine for real-world cancer theranostics.
引用
收藏
页码:2406 / 2426
页数:21
相关论文
共 146 条
[1]   Recent Progress in Electrochemical Biosensors for Glycoproteins [J].
Akiba, Uichi ;
Anzai, Jun-ichi .
SENSORS, 2016, 16 (12)
[2]  
Ali MM, 2020, TALANTA
[3]   Boronoisophthalic acid as a novel affinity ligand for the selective capture and release of glycoproteins near physiological pH [J].
Ali, Muhammad Mujahid ;
Hussain, Dilshad ;
Tang, Yan ;
Sun, Xuechun ;
Shen, Zhengchao ;
Zhang, Fengxia ;
Du, Zhenxia .
TALANTA, 2021, 225
[4]   Melamine foam assisted in-tip packed amine-functionalized titanium metal-organic framework for the selective enrichment of endogenous glycopeptides [J].
Ali, Muhammad Mujahid ;
Zhu, Zhiyuan ;
Wang, Mengyu ;
Hussain, Dilshad ;
Gao, Xia ;
Wang, Jianfeng ;
Du, Zhenxia .
JOURNAL OF CHROMATOGRAPHY A, 2021, 1636
[5]   Diethylenetriamine assisted functionalization of boronic acid on poly GMA-MAA-DVB for selective enrichment of glycoproteins and glycopeptides [J].
Ali, Muhammad Mujahid ;
Hussain, Dilshad ;
Xu, Bin ;
Sun, Tangqiang ;
Du, Zhenxia .
TALANTA, 2020, 219
[6]   Mesoporous silica and organosilica materials - Review of their synthesis and organic functionalization [J].
Asefa, Tewodros ;
Tao, Zhimin .
CANADIAN JOURNAL OF CHEMISTRY, 2012, 90 (12) :1015-1031
[7]   ANTIBODY ANARCHY: A CALL TO ORDER [J].
Baker, Monya .
NATURE, 2015, 527 (7579) :545-551
[8]   BLAME IT ON THE ANTIBODIES [J].
Baker, Monya .
NATURE, 2015, 521 (7552) :274-276
[9]  
Barthélémy P, 2014, ANTICANCER RES, V34, P1483
[10]   Novel anticancer targets: revisiting ERBB2 and discovering ERBB3 [J].
Baselga, Jose ;
Swain, Sandra M. .
NATURE REVIEWS CANCER, 2009, 9 (07) :463-475