Hyaluronan Brush-like Copolymers Promote CD44 Declustering in Breast Cancer Cells

被引:1
|
作者
Carvalho, Ana M. [1 ,2 ]
Valcarcel, Jesus [3 ]
da Costa, Diana Soares [1 ,2 ]
Gomes, Marisa [1 ,2 ]
Vazquez, Jose Antonio [3 ]
Reis, Rui L. [1 ,2 ]
Novoa-Carballal, Ramon [1 ,2 ]
Pashkuleva, Iva [1 ,2 ]
机构
[1] Univ Minho, I3Bs Res Inst Biomat Biodegradables & Biomimet, Headquarters European Inst Excellence Tissue Engn, 3Bs Res Grp, P-4805017 Barco, Portugal
[2] ICVS 3Bs PT Govt Associate Lab, P-4710057 Braga, Portugal
[3] Inst Invest Marinas IIM CSIC, Grp Reciclado & Valorizac Mat Residuales REVAL, Vigo 36208, Galicia, Spain
关键词
hyaluronic acid; end-on modification; oxime ligation; hyaluronidase; isothermal titration calorimetry; surface plasmon resonance; cancer therapy; CD44; antagonist; MOLECULAR-WEIGHT; CD44-HYALURONAN INTERACTIONS; BLOCK-COPOLYMERS; BINDING DOMAIN; TUMOR-GROWTH; PEPTIDE; METASTASIS; EXPRESSION; KINETICS; OLIGOSACCHARIDES;
D O I
10.1021/acsami.2c11864
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We report on the synthesis of hyaluronan (HA) brush-like copolymers and their application as antagonists of tumorigenic CD44-HA interactions. HA (4.8 kDa, ca. 24 saccharides) was grafted on 2-hydrohyethyl methacrylate (HEMA) by end-on oxime ligation. The obtained copolymers were compared with low and high molecular weight HA in terms of hydrolysis kinetics in the presence of hyaluronidase (isothermal titration calorimetry) and interactions with CD44 (surface plasmon resonance). The results evidenced that the high molecular weight HA and HA-g-HEMA have a much higher affinity to CD44 than low molecular weight HA. Additionally, slower enzymatic degradation was observed for the copolymer, making it an excellent candidate for active targeting of tumorigenic CD44-HA interactions. We, therefore, investigated the effect of the copolymer on cancer cell lines with different expression of CD44 and observed an efficient declustering of CD44 that is usually associated with reduction of metastasis and drug resistance.
引用
收藏
页码:41779 / 41789
页数:11
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