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Combining carbonic anhydrase and thioredoxin reductase inhibitory motifs within a single molecule dramatically increases its cytotoxicity.


ABSTRACT: A hypothesis that simultaneous targeting cancer-related carbonic anhydrase hCA IX and hCA XII isoforms (whose overexpression is a cancer cell's defence mechanism against hypoxia) along with thioredoxin reductase (overexpressed in cancers as a defence against oxidative stress) may lead to synergistic antiproliferative effects was confirmed by testing combinations of the two inhibitor classes against pancreatic cancer cells (PANC-1). Combining both pharmacophoric motifs within one molecule led to a sharp increase of cytotoxicity. This preliminary observation sets the ground for a fundamentally new approach to anticancer agent design.

SUBMITTER: Krasavin M 

PROVIDER: S-EPMC7067156 | biostudies-literature | 2020 Dec

REPOSITORIES: biostudies-literature

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Combining carbonic anhydrase and thioredoxin reductase inhibitory motifs within a single molecule dramatically increases its cytotoxicity.

Krasavin Mikhail M   Sharonova Tatiana T   Sharoyko Vladimir V   Zhukovsky Daniil D   Kalinin Stanislav S   Žalubovskis Raivis R   Tennikova Tatiana T   Supuran Claudiu T CT  

Journal of enzyme inhibition and medicinal chemistry 20201201 1


A hypothesis that simultaneous targeting cancer-related carbonic anhydrase <i>h</i>CA IX and <i>h</i>CA XII isoforms (whose overexpression is a cancer cell's defence mechanism against hypoxia) along with thioredoxin reductase (overexpressed in cancers as a defence against oxidative stress) may lead to synergistic antiproliferative effects was confirmed by testing combinations of the two inhibitor classes against pancreatic cancer cells (PANC-1). Combining both pharmacophoric motifs within one mo  ...[more]

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