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Kinomic profiling of tumour xenografts derived from patients with non-small cell lung cancer confirms their fidelity and reveals potentially actionable pathways.
- Source :
-
European journal of cancer (Oxford, England : 1990) [Eur J Cancer] 2021 Feb; Vol. 144, pp. 17-30. Date of Electronic Publication: 2020 Dec 11. - Publication Year :
- 2021
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Abstract
- Introduction: High fidelity between non-small cell lung cancer (NSCLC) primary tumours and patient-derived tumour xenografts (PDTXs) is of paramount relevance to spur their application. Extensive proteomic and kinomic analysis of these preclinical models are missing and may inform about their functional status, in terms of phosphopeptides and hyperactive signalling pathways.<br />Methods: We investigated tumour xenografts derived from patients with NSCLC to identify hyperactive signalling pathways. Fresh tumour fragments from 81 NSCLC surgical samples were implanted in Nod/Scid/Gamma mice, and engrafted tumours were compared with primary specimens by morphology, immunohistochemistry, gene mutation analyses, and kinase activity profiling. Four different tyrosine and serine/threonine kinase inhibitors were tested against primary tumour and PDTX lysates using the PamGene peptide microarray platform.<br />Results: The engraftment rate was 33%, with successful engraftment being more associated with poor clinical outcomes. Genomic profiles led to the recognition of hotspot mutations, some of which were initially undetected in donor samples. Kinomic analyses showed that characteristics of primary tumours were retained in PDTXs, and tyrosine kinase inhibitors (TKIs) responses of individual PDTX lines were either expected, based on the genetic status, or alternatively defined suitable targets unpredictable by single-genome fingerprints.<br />Conclusions: Collectively, PDTXs mostly resembled their parental NSCLC. Combining genomic and kinomic analyses of tumour xenografts derived from patients with NSCLC, we identified patients' specific targetable pathways, confirming PDTXs as a preclinical tool for biomarker identification and therapeutic algorithm'' improvement.<br />Competing Interests: Conflict of interest statement The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: A van den Berg, Rob Ruijtenbeek, Rik de Wijn and Riet Hilhorst are/were employees of PamGene International BV. All other authors have nothing to declare.<br /> (Copyright © 2020 Elsevier Ltd. All rights reserved.)
- Subjects :
- Aged
Animals
Apoptosis
Carcinoma, Non-Small-Cell Lung drug therapy
Carcinoma, Non-Small-Cell Lung enzymology
Cell Proliferation
Female
Humans
Lung Neoplasms drug therapy
Lung Neoplasms enzymology
Male
Mice
Mice, Inbred NOD
Mice, SCID
Prognosis
Protein Kinases chemistry
Survival Rate
Tumor Cells, Cultured
Xenograft Model Antitumor Assays
Carcinoma, Non-Small-Cell Lung pathology
Gene Expression Regulation, Enzymologic
Gene Expression Regulation, Neoplastic
Lung Neoplasms pathology
Protein Kinase Inhibitors therapeutic use
Protein Kinases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0852
- Volume :
- 144
- Database :
- MEDLINE
- Journal :
- European journal of cancer (Oxford, England : 1990)
- Publication Type :
- Academic Journal
- Accession number :
- 33316635
- Full Text :
- https://doi.org/10.1016/j.ejca.2020.10.036