Fast fluorescence in situ hybridisation for the enhanced detection of MET in non-small cell lung cancer.

The c-Met/hepatocyte growth factor receptor pathway is frequently dysregulated in multiple cancer types, including non-small cell lung cancer (NSCLC). MET amplification has been shown to develop as a resistance mechanism to treatment in NSCLC. The identification of increased MET copy number within t...

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Main Authors: David Jonathan Duncan, Michel Erminio Vandenberghe, Marietta Louise Juanita Scott, Craig Barker
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0223926
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spelling doaj-225bd644a1054973b44acb20fa3028c42021-03-03T21:11:56ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-011410e022392610.1371/journal.pone.0223926Fast fluorescence in situ hybridisation for the enhanced detection of MET in non-small cell lung cancer.David Jonathan DuncanMichel Erminio VandenbergheMarietta Louise Juanita ScottCraig BarkerThe c-Met/hepatocyte growth factor receptor pathway is frequently dysregulated in multiple cancer types, including non-small cell lung cancer (NSCLC). MET amplification has been shown to develop as a resistance mechanism to treatment in NSCLC. The identification of increased MET copy number within tumour cells is increasingly important to stratify those tumours and patients which are susceptible to treatment targetting MET kinase inhibition. Fluorescence in situ hybridisation (FISH) has been successfully employed to identify patients with abnormal MET gene copy number with numerous probes available for use. Here we report a FISH protocol that reduces probe hybridisation time in NSCLC tissue to 1 hour and compare the results with other protocols. MET gene copy number was determined in 20 NSCLC cases using 3 FISH probes: 1. Kreatech FISH, MET (7q31) SE 7 ready to use probes, hybridised using an overnight protocol; 2. Dako MET IQFISH probe with CEP7 ready to use probe, hybridised for 2 hours; 3. Kreatech MET (7q31) SE 7 XL FISH probe, prepared in SwiftFISH buffer and hybridised for 1 hour. The MET gene copy number and MET: centromere 7 gene ratio were determined for each tissue and cases categorised as having MET high or MET low status. All three FISH probes were shown to demonstrate good agreement with each other. Overall percentage agreement between probes was ≥90%. Intraclass correlation showed good agreement (ICC ≥0.80) between all three assays for MET gene copy number and MET: centromere 7 gene ratio. These FISH protocols provide evidence that rapid laboratory developed FISH assays with short turnaround time perform consistently with standard protocols, potentially enabling faster treatment decisions.https://doi.org/10.1371/journal.pone.0223926
collection DOAJ
language English
format Article
sources DOAJ
author David Jonathan Duncan
Michel Erminio Vandenberghe
Marietta Louise Juanita Scott
Craig Barker
spellingShingle David Jonathan Duncan
Michel Erminio Vandenberghe
Marietta Louise Juanita Scott
Craig Barker
Fast fluorescence in situ hybridisation for the enhanced detection of MET in non-small cell lung cancer.
PLoS ONE
author_facet David Jonathan Duncan
Michel Erminio Vandenberghe
Marietta Louise Juanita Scott
Craig Barker
author_sort David Jonathan Duncan
title Fast fluorescence in situ hybridisation for the enhanced detection of MET in non-small cell lung cancer.
title_short Fast fluorescence in situ hybridisation for the enhanced detection of MET in non-small cell lung cancer.
title_full Fast fluorescence in situ hybridisation for the enhanced detection of MET in non-small cell lung cancer.
title_fullStr Fast fluorescence in situ hybridisation for the enhanced detection of MET in non-small cell lung cancer.
title_full_unstemmed Fast fluorescence in situ hybridisation for the enhanced detection of MET in non-small cell lung cancer.
title_sort fast fluorescence in situ hybridisation for the enhanced detection of met in non-small cell lung cancer.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description The c-Met/hepatocyte growth factor receptor pathway is frequently dysregulated in multiple cancer types, including non-small cell lung cancer (NSCLC). MET amplification has been shown to develop as a resistance mechanism to treatment in NSCLC. The identification of increased MET copy number within tumour cells is increasingly important to stratify those tumours and patients which are susceptible to treatment targetting MET kinase inhibition. Fluorescence in situ hybridisation (FISH) has been successfully employed to identify patients with abnormal MET gene copy number with numerous probes available for use. Here we report a FISH protocol that reduces probe hybridisation time in NSCLC tissue to 1 hour and compare the results with other protocols. MET gene copy number was determined in 20 NSCLC cases using 3 FISH probes: 1. Kreatech FISH, MET (7q31) SE 7 ready to use probes, hybridised using an overnight protocol; 2. Dako MET IQFISH probe with CEP7 ready to use probe, hybridised for 2 hours; 3. Kreatech MET (7q31) SE 7 XL FISH probe, prepared in SwiftFISH buffer and hybridised for 1 hour. The MET gene copy number and MET: centromere 7 gene ratio were determined for each tissue and cases categorised as having MET high or MET low status. All three FISH probes were shown to demonstrate good agreement with each other. Overall percentage agreement between probes was ≥90%. Intraclass correlation showed good agreement (ICC ≥0.80) between all three assays for MET gene copy number and MET: centromere 7 gene ratio. These FISH protocols provide evidence that rapid laboratory developed FISH assays with short turnaround time perform consistently with standard protocols, potentially enabling faster treatment decisions.
url https://doi.org/10.1371/journal.pone.0223926
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