Akademik Veri Yönetim Sistemi
INDIAN JOURNAL OF EXPERIMENTAL BIOLOGY, cilt.63, sa.1, ss.52-65, 2025 (SCI-Expanded)
Present study, we aimed to manipulate the BCR::ABL1 fusion gene, which is responsible for the etiopathogenesis of Chronic myeloid leukemia (CML), in vitro. Mechanism of this molecular pathogenesis is based on encoding the BCR::ABL1p210 oncoprotein with excessive and irregular tyrosine kinase activity and eventually causes the CML phenotype. On the other hand, patients developing drug resistance or the side effects of bone marrow transplantation on mortality and morbidity strengthened our hypothesis that CRISPR/Cas9 could be an advance in preclinical studies in this research. Cytogenetic and molecular genetic characterization of K562 cells has been performed. Intronic sequences were detected by sequencing in the translocation of the BCR::ABL1 fusion gene. Genome editing in CML cells was done by transfection of lipofectamine and electroporation. The efficiency of CRISPR/Cas9 on the BCR::ABL1p210 was analyzed by qRT-PCR. Gene expression of the BCR::ABL1p210 fusion before and after CRISPR/Cas9 manipulation, which changed during the culture time, was compared logarithmic over the transcript values in the molecular response. We recorded that BCR::ABL1p210 manipulation showed an approximately 100-fold decrease in expression as (+1 log) before (-1 log) after CRISPR/Cas9 manipulation. Thus, the BCR::ABL1p210 fusion gene expression was significantly decreased by mediated CRISPR/Cas9 manipulation. As a result, the effect of the CRISPR/Cas9 genome editing was revealed via the knockdown of the BCR::ABL1p210 in our study. Thus, CRISPR/Cas9 can target the BCR::ABL1p210 fusion gene due to the interference effect.