| Literature DB >> 36271018 |
Jurgita Matulienė1, Gediminas Žvinys1, Vytautas Petrauskas1, Agnė Kvietkauskaitė1, Audrius Zakšauskas1, Kirill Shubin2, Asta Zubrienė1, Lina Baranauskienė1, Lina Kačenauskaitė1, Sergei Kopanchuk3, Santa Veiksina3, Vaida Paketurytė-Latvė1, Joana Smirnovienė1, Vaida Juozapaitienė1, Aurelija Mickevičiūtė1, Vilma Michailovienė1, Jelena Jachno1, Dovilė Stravinskienė4, Aistė Sližienė4, Agnė Petrošiūtė1, Holger M Becker5, Justina Kazokaitė-Adomaitienė1,6, Ala Yaromina7, Edita Čapkauskaitė1, Ago Rinken3, Virginija Dudutienė1, Ludwig J Dubois7, Daumantas Matulis8.
Abstract
Numerous human cancers, especially hypoxic solid tumors, express carbonic anhydrase IX (CAIX), a transmembrane protein with its catalytic domain located in the extracellular space. CAIX acidifies the tumor microenvironment, promotes metastases and invasiveness, and is therefore considered a promising anticancer target. We have designed a series of high affinity and high selectivity fluorescein-labeled compounds targeting CAIX to visualize and quantify CAIX expression in cancer cells. The competitive binding model enabled the determination of common CA inhibitors' dissociation constants for CAIX expressed in exponentially growing cancer cells. All tested sulfonamide compounds bound the proliferating cells with similar affinity as to recombinantly purified CAIX. The probes are applicable for the design of selective drug-like compounds for CAIX and the competition strategy could be applied to other drug targets.Entities:
Year: 2022 PMID: 36271018 DOI: 10.1038/s41598-022-22436-1
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.996