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Статья

Combination of Carbonic Anhydrase Isoform IX Inhibitors and Gefitinib Suppresses on the Invasive Potential of Non-Small Cell Lung Cancer Cells

Alexander S. BunevMedicinal Chemistry Center, Togliatti State University, Togliatti, 445020, RussiaАнтон А. ШетневInstitute of Biophysics of the Future, Dolgoprudny, Moscow Region, 141701, RussiaOlga S. ShemchukPavlov First St. Petersburg State Medical University, St. Petersburg, 197022, RussiaPavel K KozhukhovPavlov First St. Petersburg State Medical University, St. Petersburg, 197022, RussiaTatiana V. SharonovaSt. Petersburg State University, St. Petersburg, 199034, RussiaIrina TyuryaevaInstitute of Cytology, Russian Academy of Sciences, St. Petersburg, 194064, RussiaMikhail KhotinInstitute of Cytology, Russian Academy of Sciences, St. Petersburg, 194064, RussiaSergey V. AgeevPavlov First St. Petersburg State Medical University, St. Petersburg, 197022, RussiaDilafruz K. KholmurodovaScientific and Practice Center for Immunology, Allergology and Human Genomics, Samarkand State Medical University, Samarkand, 100400, UzbekistanJasur A RizaevScientific and Practice Center for Immunology, Allergology and Human Genomics, Samarkand State Medical University, Samarkand, 100400, UzbekistanKonstantin N. SemenovPavlov First St. Petersburg State Medical University, St. Petersburg, 197022, RussiaVladimir V. SharoykoMedicinal Chemistry Center, Togliatti State University, Togliatti, 445020, Russia. [email protected]
Biochemistry (Moscow)journal2024en
ABI

Аннотация

Human carbonic anhydrase IX (CAIX) plays a key role in maintaining pH homeostasis of malignant neoplasms, thus creating a favorable microenvironment for the growth, invasion, and metastasis of tumor cells. Recent studies have established that inhibition of CAIX expressed on the surface of tumor cells significantly increases the efficacy of classical chemotherapeutic agents and makes it possible to suppress the resistance of tumor cells to chemotherapy, as well as to increase their sensitivity to drugs (in particular, to reduce the required dose of cytostatic agents). In this work, we studied the ability of new CAIX inhibitors based on substituted 1,2,4-oxadiazole-containing primary aromatic sulfonamides, to potentiate the cytostatic effect of gefitinib (selective inhibitor of epidermal growth factor receptor tyrosine kinase domain) under hypoxic conditions. We investigated a combined effect of gefitinib and CAIX inhibitors 4-(3-phenyl-1,2,4-oxadiazol-5-yl)thiophene-2-sulfonamide (1), 4-(5-(thiophene-3-yl)-1,2,4-oxadiazol-3-yl)benzenesulfonamide (2), 4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)thiophene-2-sulfonamide (3), and 4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenesulfonamide (4) on gefitinib cytotoxicity, cell proliferation, activation of caspases-3/7, and cell cycle control in human lung adenocarcinoma A549 cells. It was found that the combinations of compounds 1 and 2 with gefitinib suppressed the invasive potential of A549 cells. Compound 1 had the greatest effect and can be considered as a promising candidate for further research.

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