Вид документа : Статья из журнала Шифр издания : Автор(ы) : Antonenko S. V., Telegeev G. D. Заглавие : Inhibition of USP1, a new partner of Bcr-Abl, results in decrease of Bcr-Abl level in K562 cells Место публикации : Experimental Oncology. - К., 2020. - Том 42, N 2. - С. 109-114 (Шифр ЕУ12/2020/42/2) MeSH-главная: ЛЕЙКОЗ МИЕЛОИДНЫЙ ХРОНИЧЕСКИЙ АТИПИЧЕСКИЙ, BCR-ABL ОТРИЦАТЕЛЬНЫЙ -- LEUKEMIA, MYELOID, CHRONIC, ATYPICAL, BCR-ABL NEGATIVE Аннотация: To analyze interaction of ubiquitin specific peptidase 1 (USP1) with Bcr-Abl and to assess the relation between USP1 functional activity and Bcr-Abl expression in K562 chronic myeloid leukemia cells. Materials and Methods: The interaction between USP1 and Bcr-Abl in K562 cells was analyzed by co-immunoprecipitation, Western blot analysis, and confocal microscopy. Results: A direct interaction between Bcr-Abl oncoprotein and USP1 protein in K562 cells was established by co-immunoprecipitation. Immunofluorescence analysis and confocal microscopy revealed that Bcr-Abl/USP1 protein complex is formed in the cell nucleus. The inhibition of USP1 protein activity by ML323 reduced the level of Bcr-Abl oncoprotein in K562 cells. Conclusions: USP1 protein has been identified as a new protein partner of Bcr-Abl oncoprotein in chronic myeloid leukemia. The relationship between the functional activity of USP1 protein and the level of Bcr-Abl oncoprotein has been demonstrated, suggesting that the targeted inhibition of USP1 activity could be a challenging approach for reducing Bcr-Abl expression Доп.точки доступа: Telegeev, G. D.