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ABL1 tyrosine kinase domain mutations in chronic myeloid leukemia treatment resistance.
Vacarean-Trandafir, Irina Cezara; Ivanov, Iuliu Cristian; Dragos, Loredana Mihaiela; Dascalescu, Angela Smaranda; Titieanu, Amalia Andrea; Cojocaru, Dumitru.
Afiliação
  • Vacarean-Trandafir IC; Department of Molecular Genetics, Research Center Transcend, Regional Institute of Oncology, General Henri Mathias Berthelot Street, No. 2-4, 700483, Iasi, Romania. trandafirina.bi@gmail.com.
  • Ivanov IC; Department of Molecular Genetics and Biochemistry, "Alexandru Ioan Cuza" University, Carol I Bd., No. 11, 700506, Iasi, Romania. trandafirina.bi@gmail.com.
  • Dragos LM; Department of Molecular Genetics, Research Center Transcend, Regional Institute of Oncology, General Henri Mathias Berthelot Street, No. 2-4, 700483, Iasi, Romania.
  • Dascalescu AS; Department of Molecular Genetics, Research Center Transcend, Regional Institute of Oncology, General Henri Mathias Berthelot Street, No. 2-4, 700483, Iasi, Romania.
  • Titieanu AA; Department of Molecular Genetics and Biochemistry, "Alexandru Ioan Cuza" University, Carol I Bd., No. 11, 700506, Iasi, Romania.
  • Cojocaru D; Department of Hematology, Regional Institute of Oncology, General Henri Mathias Berthelot Street, No. 2-4, 700483, Iasi, Romania.
Mol Biol Rep ; 46(4): 3747-3754, 2019 Aug.
Article em En | MEDLINE | ID: mdl-31025148
The development of mutations in the BCR-ABL1 fusion gene transcript causes resistance to tyrosine kinase inhibitors (TKIs) based therapy in chronic myeloid leukemia (CML). Thereby, screening for BCR-ABL1 mutations is advised especially in patients undergoing poor response to treatment. In the current study the authors investigated 43 patients with CML that failed or had suboptimal response to TKIs treatment. Blood samples were collected from patients that were treated with TKIs. The analysis of genetic mutations was performed using a semi-nested PCR assay, followed by Sanger sequencing. The analysis revealed 15 mutations (32.55%): 14 point mutations and an exon 7 deletion. In roughly 30% of cases, mutations in the BCR-ABL1 fusion gene are common causes for treatment resistance.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Mielogênica Crônica BCR-ABL Positiva / Proteínas de Fusão bcr-abl / Resistencia a Medicamentos Antineoplásicos Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Biol Rep Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Romênia

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Mielogênica Crônica BCR-ABL Positiva / Proteínas de Fusão bcr-abl / Resistencia a Medicamentos Antineoplásicos Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Biol Rep Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Romênia