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المؤلفMohamed A., Ismail
المؤلفNasrallah, Gheyath K.
المؤلفMonne, Maria
المؤلفAlSayab, Ali
المؤلفYassin, Mohamed A.
المؤلفVaradharaj, Govindarajulu
المؤلفYounes, Salma
المؤلفSorio, Claudio
المؤلفCook, Richard
المؤلفModjtahedi, Helmout
المؤلفAl-Dewik, Nader I.
تاريخ الإتاحة2022-02-22T10:59:45Z
تاريخ النشر2022-03-01
اسم المنشورGene
المعرّفhttp://dx.doi.org/10.1016/j.gene.2021.146101
الاقتباسIsmail, M. A., Nasrallah, G. K., Monne, M., AlSayab, A., Yassin, M. A., Varadharaj, G., Younes, S., Sorio, C., Cook, R., Modjtahedi, H., & Al-Dewik, N. I. (2022). Description of PTPRG genetic variants identified in a cohort of Chronic Myeloid Leukemia patients and their ability to influence response to Tyrosine kinase Inhibitors. Gene, 813, 146101. https://doi.org/10.1016/j.gene.2021.146101
الرقم المعياري الدولي للكتاب03781119
معرّف المصادر الموحدhttps://www.sciencedirect.com/science/article/pii/S037811192100696X
معرّف المصادر الموحدhttp://hdl.handle.net/10576/27395
الملخصTyrosine kinase inhibitors (TKIs) have remarkably transformed Ph+ chronic myeloid leukemia (CML) management; however, TKI resistance remains a major clinical challenge. Mutations in BCR-ABL1 are well studied but fail to explain 20–40% of resistant cases, suggesting the activation of alternative, BCR-ABL1-independent pathways. Protein Tyrosine Phosphatase Receptor Gamma (PTPRG), a tumor suppressor, was found to be well expressed in CML patients responsive to TKIs and remained at low level in resistant patients. In this study, we aimed to identify genetic variants in PTPRG that could potentially modulate TKIs response in CML patients. DNA was extracted from peripheral blood samples collected from two CML cohorts (Qatar and Italy) and targeted exome sequencing was performed. Among 31 CML patients, six were TKI-responders and 25 were TKI-non-responsive. Sequencing identified ten variants, seven were annotated and three were novel SNPs (c.1602_1603insC, c.85+14412delC, and c.2289-129delA). Among them, five variants were identified in 15 resistant cases. Of these, one novel exon variant (c.1602_1603insC), c.841-29C>T (rs199917960) and c.1378-224A>G (rs2063204) were found to be significantly different between the resistant cases compared to responders. Our findings suggest that PTPRG variants may act as an indirect resistance mechanism of BCR-ABL1 to affect TKI treatment.
راعي المشروعThis work was supported by the National Priorities Research Program (NPRP) grant number 4-157-3–052.
اللغةen
الناشرElsevier
الموضوعChronic Myeloid Leukemia
Protein Tyrosine Phosphatase Receptor Type G
BCR-ABL1
Single Nucleotide Polymorphisms
Tyrosine Kinase Inhibitors
Therapeutic Modalities
العنوانDescription of PTPRG genetic variants identified in a cohort of Chronic Myeloid Leukemia patients and their ability to influence response to Tyrosine kinase Inhibitors
النوعArticle
رقم المجلد813
Open Access user License http://creativecommons.org/licenses/by/4.0/
dc.accessType Open Access


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