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Frequent activating STAT3 mutations and novel recurrent genomic abnormalities detected in breast implant-associated anaplastic large cell lymphoma.

Authors :
Blombery P
Thompson E
Ryland GL
Joyce R
Byrne DJ
Khoo C
Lade S
Hertzberg M
Hapgood G
Marlton P
Deva A
Lindeman G
Fox S
Westerman D
Prince M
Source :
Oncotarget [Oncotarget] 2018 Nov 16; Vol. 9 (90), pp. 36126-36136. Date of Electronic Publication: 2018 Nov 16 (Print Publication: 2018).
Publication Year :
2018

Abstract

Breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) is a rare form of T-cell lymphoma that occurs after implantation of breast prostheses. We performed comprehensive next generation sequencing based genomic characterization of 11 cases of BIA-ALCL including sequence variant detection on 180 genes frequently mutated in haematological malignancy, genome-wide copy number assessment, structural variant detection involving the T-cell receptor loci and TRB deep-sequencing. We observed sequence variants leading to JAK/STAT activation in 10 out of 11 patients. We also observed germline TP53 mutations in two cases. In addition we detected a recurrent copy number loss involving RPL5 as well as copy number amplifications involving TNFRSF11A [RANK] (in 2 cases), MYC , P2RX7 , TMEM119 and PDGFRA . In summary, our comprehensive genomic characterisation of 11 cases of BIA-ALCL has provided insight into potential pathobiological mechanisms (JAK/STAT, MYC and TP53) as well as identifying targets for future therapeutic intervention (TNFRSF11A, PDGFRA) in this rare entity.<br />Competing Interests: CONFLICTS OF INTEREST The authors have no conflicts of interest to declare.

Details

Language :
English
ISSN :
1949-2553
Volume :
9
Issue :
90
Database :
MEDLINE
Journal :
Oncotarget
Publication Type :
Academic Journal
Accession number :
30546832
Full Text :
https://doi.org/10.18632/oncotarget.26308