دورية أكاديمية

Challenging perspectives on the cellular origins of lymphoma.

التفاصيل البيبلوغرافية
العنوان: Challenging perspectives on the cellular origins of lymphoma.
المؤلفون: Malcolm TI; Division of Molecular Histopathology, Department of Pathology, University of Cambridge, Lab Block Level 3, Box 231, Addenbrooke's Hospital, Cambridge CB2 0QQ, UK., Hodson DJ; Department of Haematology, University of Cambridge, Cambridge, UK., Macintyre EA; Hematology and INSERM1151, Institut Necker-Enfants Malades, Université Sorbonne Paris Cité at Descartes and Assistance Publique-Hôpitaux de Paris, Paris 75743 Cedex 15, France., Turner SD; Division of Molecular Histopathology, Department of Pathology, University of Cambridge, Lab Block Level 3, Box 231, Addenbrooke's Hospital, Cambridge CB2 0QQ, UK sdt36@cam.ac.uk.
المصدر: Open biology [Open Biol] 2016 Sep; Vol. 6 (9).
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Royal Society Pub Country of Publication: England NLM ID: 101580419 Publication Model: Print Cited Medium: Internet ISSN: 2046-2441 (Electronic) Linking ISSN: 20462441 NLM ISO Abbreviation: Open Biol Subsets: PubMed not MEDLINE
أسماء مطبوعة: Original Publication: London : Royal Society Pub., [2011]-
مستخلص: Both B and T lymphocytes have signature traits that set them apart from other cell types. They actively and repeatedly rearrange their DNA in order to produce a unique and functional antigen receptor, they have potential for massive clonal expansion upon encountering antigen via this receptor or its precursor, and they have the capacity to be extremely long lived as 'memory' cells. All three of these traits are fundamental to their ability to function as the adaptive immune response to infectious agents, but concurrently render these cells vulnerable to transformation. Thus, it is classically considered that lymphomas arise at a relatively late stage in a lymphocyte's development during the process of modifying diversity within antigen receptors, and when the cell is capable of responding to stimulus via its receptor. Attempts to understand the aetiology of lymphoma have reinforced this notion, as the most notable advances to date have shown chronic stimulation of the antigen receptor by infectious agents or self-antigens to be key drivers of these diseases. Despite this, there is still uncertainty about the cell of origin in some lymphomas, and increasing evidence that a subset arises in a more immature cell. Specifically, a recent study indicates that T-cell lymphoma, in particular nucleophosmin-anaplastic lymphoma kinase-driven anaplastic large cell lymphoma, may originate in T-cell progenitors in the thymus.
(© 2016 The Authors.)
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معلومات مُعتمدة: MC_PC_12009 United Kingdom MRC_ Medical Research Council; MR/M008584/1 United Kingdom MRC_ Medical Research Council
فهرسة مساهمة: Keywords: T cell; anaplastic large cell lymphoma; lymphomagenesis
تواريخ الأحداث: Date Created: 20160930 Latest Revision: 20220131
رمز التحديث: 20240829
مُعرف محوري في PubMed: PMC5043587
DOI: 10.1098/rsob.160232
PMID: 27683157
قاعدة البيانات: MEDLINE
الوصف
تدمد:2046-2441
DOI:10.1098/rsob.160232