Your browser doesn't support javascript.
loading
Clinical and laboratory relevance of JAK2 V617F and BCR-ABL co-existence in Philadelphia positive CML patients.
Ahmad, Nasir; Qayum, Saima; Jameel, Abid; Ali, Asif; Siraj, Sami; Ali, Johar; Yousafzai, Yasar Mehmood.
Affiliation
  • Ahmad N; Institue of Basic Medical Sciences, Khyber Medical University (IBMS-KMU), Peshawar, KP, Pakistan.
  • Qayum S; Institue of Basic Medical Sciences, Khyber Medical University (IBMS-KMU), Peshawar, KP, Pakistan.
  • Jameel A; Medical Teaching Institute, Hayatabad Medical Complex (MTI-HMC), Hayatabad, Peshawar, KP, Pakistan.
  • Ali A; Institute of Pathology and Diagnostic Medicine, Khyber Medical University (IPDM-KMU), Peshawar, KP, Pakistan/College of Medical, Veterinary & Life Sciences, University of Glasgow, Glasgow, United Kingdom.
  • Siraj S; Institue of Basic Medical Sciences, Khyber Medical University (IBMS-KMU), Peshawar, KP, Pakistan.
  • Ali J; Center for Genomic Sciences, Rehman Medical Institute (RMI), Hayatabad, Peshawar, KP, Pakistan.
  • Yousafzai YM; Institute of Pathology and Diagnostic Medicine, Khyber Medical University (IPDM-KMU), Peshawar, KP, Pakistan/College of Medical, Veterinary & Life Sciences, University of Glasgow, Glasgow, United Kingdom.
Pak J Pharm Sci ; 34(6(Supplementary)): 2289-2295, 2021 Nov.
Article in En | MEDLINE | ID: mdl-35039265
Chronic Myeloid Leukaemia (CML) is characterized by BCR-ABL1 mutation. A number of research studies have published reports of concomitant JAK2-V617F mutation in BCR-ABL positive Chronic Myeloid Leukaemia. This study aims to investigate the frequency of JAK2-V617F mutation in BCR-ABL positive CML cases. After approval from ethical committee, participants were enrolled in the study. A total of 103 samples from CML patients were analysed for the presence of JAK2-V617F mutation using real-time polymerase chain reaction. Patients were monitored for treatment response using real-time quantitative PCR for BCR-ABL1 mutation. Out of 103 samples analysed, 2 patients tested positive for JAK2-V617F mutation. These two patients when treated with standard Tyrosine Kinase Inhibitors (TKI) therapy achieved molecular response and normalized the haemoglobin and white cell counts. However, one patient has sustained thrombocytosis. JAK2 remained positive throughout the treatment course. We could not follow the second patient till the end of the study. JAK2 mutation in BCR-ABL1 mutated CML appears to be rare. Treatment with TKI does not appear to reduce JAK2 mutation burden despite a decrease in BCR-ABL1 copy numbers.
Subject(s)
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Leukemia, Myelogenous, Chronic, BCR-ABL Positive / Biomarkers, Tumor / Fusion Proteins, bcr-abl / Janus Kinase 2 / Mutation Type of study: Observational_studies Aspects: Ethics Limits: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Language: En Journal: Pak J Pharm Sci Journal subject: FARMACIA / FARMACOLOGIA / QUIMICA Year: 2021 Document type: Article Affiliation country: Pakistan Country of publication: Pakistan
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Leukemia, Myelogenous, Chronic, BCR-ABL Positive / Biomarkers, Tumor / Fusion Proteins, bcr-abl / Janus Kinase 2 / Mutation Type of study: Observational_studies Aspects: Ethics Limits: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Language: En Journal: Pak J Pharm Sci Journal subject: FARMACIA / FARMACOLOGIA / QUIMICA Year: 2021 Document type: Article Affiliation country: Pakistan Country of publication: Pakistan