Adenylate kinase immobilized on graphene oxide impairs progression of human lung carcinoma epithelial cells through adenosinergic pathway

被引:1
作者
Anna, Hetmann [1 ]
Bartosz, Szymczak [1 ]
Joanna, Czarnecka [1 ]
Tomasz, Rusak [2 ]
Marek, Wisniewski [3 ]
Magdalena, Wujak [4 ]
Katarzyna, Roszek [1 ,5 ]
机构
[1] Nicolaus Copernicus Univ Torun, Fac Biol & Vet Sci, Dept Biochem, Torun, Poland
[2] Med Univ Bialystok, Fac Pharm, Dept Phys Chem, Bialystok, Poland
[3] Nicolaus Copernicus Univ Torun, Fac Chem, Dept Mat Chem Adsorpt & Catalysis, Torun, Poland
[4] Nicolaus Copernicus Univ Torun, Fac Pharm, Dept Med Chem, Coll Medicum Bydgoszcz, Bydgoszcz, Poland
[5] Nicolaus Copernicus Univ Torun, Fac Biol & Vet Sci, Dept Biochem, Lwowska 1, PL-87100 Torun, Poland
关键词
adenosine; adenylate kinase; anti-cancer activity; graphene oxide; immobilization; purinergic signaling; EXTRACELLULAR NUCLEOTIDES; RECEPTOR EXPRESSION; METABOLISM; ATP; NUCLEOSIDES;
D O I
10.1002/jbm.a.37555
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Purinergic signaling, the oldest evolutionary transmitter system, has been increasingly studied as a pivotal target for novel anti-cancer therapies. In the present work, the developed nanobiocatalytic system consisting of adenylate kinase immobilized on graphene oxide (AK-GO) was characterized in terms of its physicochemical and biochemical properties. We put special emphasis on the AK-GO influence on purinergic signaling components, that is, ecto-nucleotides concentration and ecto-enzymes expression and activity in human lung carcinoma epithelial (A549) cells. The immobilization-dependent modification of AK kinetic parameters allowed for the removal of ATP excess while maintaining low ATP concentrations, efficient decrease in adenosine concentration, and control of the nucleotide balance in carcinoma cells. The cyto- and hemocompatibility of developed AK-GO nanobiocatalytic system indicates that it can be successfully harnessed for biomedical applications. In A549 cells treated with AK-GO nanobiocatalytic system, the significantly decreased adenosinergic signaling results in reduction of the proliferation and migration capability of cancer cells. This finding is particularly relevant in regard to AK-GO prospective anti-cancer applications.
引用
收藏
页码:1565 / 1576
页数:12
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