首页 | 本学科首页   官方微博 | 高级检索  
检索        


CD274 (PDL1) and JAK2 genomic amplifications in pulmonary squamous‐cell and adenocarcinoma patients
Authors:Sergi Clavé  Lara Pijuan  David Casadevall  Álvaro Taus  Javier Gimeno  Silvia Hernández‐Llodrà  María Rodríguez‐Rivera  Marta Lorenzo  Silvia Menéndez  Joan Albanell  Blanca Espinet  Edurne Arriola  Marta Salido
Institution:1. Laboratori de Citogenètica Molecular, Servei de Patologia, Hospital del Mar, Barcelona, Spain;2. Programa de Recerca en Càncer, IMIM (Institut Mar d'Investigacions Mèdiques), Barcelona, Spain;3. Servei de Patologia, Hospital del Mar, Barcelona, Spain;4. Servei d'Oncologia Mèdica, Hospital del Mar, Barcelona, Spain;5. Department of Health and Experimental Sciences, Universitat Pompeu Fabra, Barcelona, Spain
Abstract:

Aims

CD274 (PDL1) and JAK2 (9p24.1) gene amplifications have been recently described in pulmonary carcinomas in association with programmed death‐ligand 1 (PD‐L1) expression. Furthermore, PTEN loss has been explored preclinically in relation to PD‐L1 expression. Our aim was to determine whether these genomic alterations affect PD‐L1 expression levels in non‐small‐cell lung cancer.

Methods and results

PD‐L1 and PTEN expression determined by immunohistochemistry (IHC), and CD274, JAK2 and PTEN copy number alterations (CNAs) determined by fluorescence in‐situ hybridisation, were studied in 171 pulmonary carcinoma specimens. PD‐L1 expression was positive in 40 cases (23.3%), and CD274 amplification was present in 14 tumours (8.8%). Concordance between both events was found in 12 of 14 amplified cases (P = 0.0001). We found nine JAK2‐amplified cases (5.7%), seven with PD‐L1 expression (P = 0.0006). Moreover, six of the seven cases had JAK2 and CD274 coamplification (9p24.1 genomic amplification). Remarkably, the average PD‐L1 IHC score was higher in these amplified cases (230 versus 80; P = 0.001). Non‐statistical associations were observed between PD‐L1 expression and PTEN loss and PTEN deletions.

Conclusions

We describe a subset of patients (8.2%) who had 9p24.1 amplifications resulting in high expression of PD‐L1. Our results provide evidence for genomic up‐regulation of PD‐L1 expression in non‐small‐cell lung cancer.
Keywords:biomarkers  DNA copy number variations  fluorescence in‐situ hybridisation  immunohistochemistry  immunotherapy
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号