| First Author | Malcolm TI | Year | 2016 |
| Journal | Nat Commun | Volume | 7 |
| Pages | 10087 | PubMed ID | 26753883 |
| Mgi Jnum | J:235890 | Mgi Id | MGI:5803915 |
| Doi | 10.1038/ncomms10087 | Citation | Malcolm TI, et al. (2016) Anaplastic large cell lymphoma arises in thymocytes and requires transient TCR expression for thymic egress. Nat Commun 7:10087 |
| abstractText | Anaplastic large cell lymphoma (ALCL) is a peripheral T-cell lymphoma presenting mostly in children and young adults. The natural progression of this disease is largely unknown as is the identity of its true cell of origin. Here we present a model of peripheral ALCL pathogenesis where the malignancy is initiated in early thymocytes, before T-cell receptor (TCR) beta-rearrangement, which is bypassed in CD4/NPM-ALK transgenic mice following Notch1 expression. However, we find that a TCR is required for thymic egress and development of peripheral murine tumours, yet this TCR must be downregulated for T-cell lymphomagenesis. In keeping with this, clonal TCR rearrangements in human ALCL are predominantly in-frame, but often aberrant, with clonal TCRalpha but no comparable clonal TCRbeta rearrangement, yielding events that would not normally be permissive for survival during thymic development. Children affected by ALCL may thus harbour thymic lymphoma-initiating cells capable of seeding relapse after chemotherapy. |
