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Phenotyping of lymphoproliferative tumours generated in xenografts of non-small cell lung cancer

Abstract:
Background: Patient-derived xenograft (PDX) models involve the engraftment of tumour tissue in immunocompromised mice and represent an important pre-clinical oncology research method. A limitation of non-small cell lung cancer (NSCLC) PDX model derivation in NOD-scid IL2Rgammanull (NSG) mice is that a subset of initial engraftments are of lymphocytic, rather than tumour origin. / Methods: The immunophenotype of lymphoproliferations arising in the lung TRACERx PDX pipeline were characterised. To present the histology data herein, we developed a Python-based tool for generating patient-level pathology overview figures from whole-slide image files; PATHOverview is available on GitHub (https://github.com/EpiCENTR-Lab/PATHOverview). / Results: Lymphoproliferations occurred in 17.8% of lung adenocarcinoma and 10% of lung squamous cell carcinoma transplantations, despite none of these patients having a prior or subsequent clinical history of lymphoproliferative disease. Lymphoproliferations were predominantly human CD20+ B cells and had the immunophenotype expected for post-transplantation diffuse large B cell lymphoma with plasma cell features. All lymphoproliferations expressed Epstein-Barr-encoded RNAs (EBER). Analysis of immunoglobulin light chain gene rearrangements in three tumours where multiple tumour regions had resulted in lymphoproliferations suggested that each had independent clonal origins. / Discussion: Overall, these data suggest that B cell clones with lymphoproliferative potential are present within primary NSCLC tumours, and that these are under continuous immune surveillance. Since these cells can be expanded following transplantation into NSG mice, our data highlight the value of quality control measures to identify lymphoproliferations within xenograft pipelines and support the incorporation of strategies to minimise lymphoproliferations during the early stages of xenograft establishment pipelines
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.3389/fonc.2023.1156743
Publication website:
https://discovery.ucl.ac.uk/10172572/1/fonc-13-1156743.pdf

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Author
ORCID:
0000-0001-8443-2924
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Role:
Author
ORCID:
0000-0003-0629-3927
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0003-4041-0867
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Role:
Author
ORCID:
0009-0005-0479-8990
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Role:
Author
ORCID:
0000-0001-8009-4999


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Funder identifier:
10.13039/100010269
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Funder identifier:
10.13039/501100000289
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Funder identifier:
10.13039/501100020252


Publisher:
Frontiers Media
Journal:
Frontiers in Oncology More from this journal
Volume:
13
Pages:
1156743-1156743
Article number:
1156743
Publication date:
2023-06-05
DOI:
EISSN:
2234-943X
ISSN:
2234-943X


Language:
English
Keywords:
Pubs id:
1490550
Local pid:
pubs:1490550
Source identifiers:
W4379472680
Deposit date:
2026-05-11
ARK identifier:
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