دورية أكاديمية
The malignant transformation potential of the oncogene STYK1/NOK at early lymphocyte development in transgenic mice.
العنوان: | The malignant transformation potential of the oncogene STYK1/NOK at early lymphocyte development in transgenic mice. |
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المؤلفون: | Yang Y; Department of Pathogen Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & School of Basic Medicine, Peking Union Medical College, Beijing, 100005, China., Liu L; Department of Pathogen Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & School of Basic Medicine, Peking Union Medical College, Beijing, 100005, China., Tucker HO; Molecular Biosciences, Institute for Cellular and Molecular Biology, University of Texas at Austin, 1 University Station A5000, Austin, TX, 78712, USA. |
المصدر: | Biochemistry and biophysics reports [Biochem Biophys Rep] 2024 Apr 12; Vol. 38, pp. 101709. Date of Electronic Publication: 2024 Apr 12 (Print Publication: 2024). |
نوع المنشور: | Journal Article |
اللغة: | English |
بيانات الدورية: | Publisher: Elsevier B.V Country of Publication: Netherlands NLM ID: 101660999 Publication Model: eCollection Cited Medium: Internet ISSN: 2405-5808 (Electronic) Linking ISSN: 24055808 NLM ISO Abbreviation: Biochem Biophys Rep Subsets: PubMed not MEDLINE |
أسماء مطبوعة: | Original Publication: [Amsterdam] : Elsevier B.V., [2015]- |
مستخلص: | B-cell Chronic Lymphocytic Leukemia (B-CLL) is a malignancy caused by the clonal expansion of mature B lymphocytes bearing a CD5 + CD19 + (B1) phenotype. However, the origin of B-CLL remains controversial. We showed previously that STYK1/NOK transgenic mice develop a CLL-like disease. Using this model system in this study, we attempt to define the stage of CLL initiation. Here, we show that the phenotype of STYK1/NOK-induced B-CLL is heterogeneous. The expanded B1 lymphocyte pool was detected within peripheral lymphoid organs and was frequently associated with the expansions of memory B cells. Despite this immunophenotypic heterogeneity, suppression of B cell development at an early stage consistently occurred within the bone marrow (BM) of STYK1/NOK-tg mice. Overall, we suggest that enforced expression of STYK1/NOK in transgenic mice might significantly predispose BM hematopoietic stem cells (HSCs) towards the development of B-CLL. Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. (© 2024 The Authors.) |
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فهرسة مساهمة: | Keywords: B lymphocyte; B1 cells; CLL; HSC; Lymphadenectasis; STYK1/NOK |
تواريخ الأحداث: | Date Created: 20240419 Latest Revision: 20240425 |
رمز التحديث: | 20240425 |
مُعرف محوري في PubMed: | PMC11024497 |
DOI: | 10.1016/j.bbrep.2024.101709 |
PMID: | 38638675 |
قاعدة البيانات: | MEDLINE |
تدمد: | 2405-5808 |
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DOI: | 10.1016/j.bbrep.2024.101709 |