Correlation between MET protein expression and MET gene copy number in a Caucasian cohort of non-small cell lung cancers according to the new IASLC/ATS/ERS classification. Issue 4 (June 2015)
- Record Type:
- Journal Article
- Title:
- Correlation between MET protein expression and MET gene copy number in a Caucasian cohort of non-small cell lung cancers according to the new IASLC/ATS/ERS classification. Issue 4 (June 2015)
- Main Title:
- Correlation between MET protein expression and MET gene copy number in a Caucasian cohort of non-small cell lung cancers according to the new IASLC/ATS/ERS classification
- Authors:
- Weingertner, Noëlle
Meyer, Nicolas
Voegeli, Anne-Claire
Guenot, Dominique
Renaud, Stéphane
Massard, Gilbert
Falcoz, Pierre-Emmanuel
Olland, Anne
Mennecier, Bertrand
Gaub, Marie-Pierre
Lindner, Véronique
Ghnassia, Jean-Pierre
Quoix, Elisabeth
Chenard, Marie-Pierre
Beau-Faller, Michèle - Abstract:
- <abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title>Summary</title> <p>MET pathway is a promising target in non-small cell lung cancers (NSCLC) requiring companion tests. The aim of this study was to compare MET expression/gene copy number in a Caucasian population of NSCLC patients.</p> <p>We analysed 201 NSCLC, with 141 adenocarcinomas classified according to 2011 IASLC recommendations, for MET expression by immunohistochemistry (IHC) and gene copy number (GCN) by silver <italic>in situ</italic> hybridisation (SISH) on tissue microarrays. Mutations in <italic>EGFR</italic>, <italic>KRAS</italic>, <italic>BRAF</italic>, <italic>HER2</italic>, <italic>PIK3CA</italic> genes and <italic>ALK</italic> rearrangements were determined.</p> <p>MET overexpression was observed in 44% and a high <italic>MET</italic> GCN (≥5 copies) in 14%. <italic>MET</italic> CGN was correlated with MET expression, regardless of IHC scores (<italic>p</italic> &lt; 0.001) but only 31% of MET overexpressed cases were SISH positive. MET overexpression/GCN number was more frequent in ADC than the other types (<italic>p</italic> &lt; 0.001), the highest in high grade (74%/34%) and sarcomatoid ADC (86%/43%). Mutations of current genes or ALK rearrangements were identified in overexpressed or amplified <italic>MET</italic> cases. MET overexpression was an independent prognostic factor for overall survival in non-smoker NSCLC in univariate (<italic>p</italic> = 0.01) and multivariate<abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title>Summary</title> <p>MET pathway is a promising target in non-small cell lung cancers (NSCLC) requiring companion tests. The aim of this study was to compare MET expression/gene copy number in a Caucasian population of NSCLC patients.</p> <p>We analysed 201 NSCLC, with 141 adenocarcinomas classified according to 2011 IASLC recommendations, for MET expression by immunohistochemistry (IHC) and gene copy number (GCN) by silver <italic>in situ</italic> hybridisation (SISH) on tissue microarrays. Mutations in <italic>EGFR</italic>, <italic>KRAS</italic>, <italic>BRAF</italic>, <italic>HER2</italic>, <italic>PIK3CA</italic> genes and <italic>ALK</italic> rearrangements were determined.</p> <p>MET overexpression was observed in 44% and a high <italic>MET</italic> GCN (≥5 copies) in 14%. <italic>MET</italic> CGN was correlated with MET expression, regardless of IHC scores (<italic>p</italic> &lt; 0.001) but only 31% of MET overexpressed cases were SISH positive. MET overexpression/GCN number was more frequent in ADC than the other types (<italic>p</italic> &lt; 0.001), the highest in high grade (74%/34%) and sarcomatoid ADC (86%/43%). Mutations of current genes or ALK rearrangements were identified in overexpressed or amplified <italic>MET</italic> cases. MET overexpression was an independent prognostic factor for overall survival in non-smoker NSCLC in univariate (<italic>p</italic> = 0.01) and multivariate (<italic>p</italic> = 0.01) analyses.</p> <p>MET overexpression is more frequent than <italic>MET</italic> high GCN, particularly in high grade ADC, regardless of <italic>EGFR, KRAS, BRAF, HER2, PIK3CA</italic> and <italic>ALK</italic> status in NSCLC.</p> </sec> </abstract> … (more)
- Is Part Of:
- Pathology. Volume 47:Issue 4(2015:Jun.)
- Journal:
- Pathology
- Issue:
- Volume 47:Issue 4(2015:Jun.)
- Issue Display:
- Volume 47, Issue 4 (2015)
- Year:
- 2015
- Volume:
- 47
- Issue:
- 4
- Issue Sort Value:
- 2015-0047-0004-0000
- Page Start:
- Page End:
- Publication Date:
- 2015-06
- Subjects:
- Pathology -- Periodicals
616.0705 - Journal URLs:
- http://informahealthcare.com/loi/pat ↗
http://journals.lww.com/pathologyrcpa/pages/issuelist.aspx ↗
http://pathologyjournal.rcpa.edu.au/ ↗
http://journals.lww.com ↗
http://www.tandf.co.uk/journals/titles/00313025.asp ↗ - DOI:
- 10.1097/PAT.0000000000000269 ↗
- Languages:
- English
- ISSNs:
- 0031-3025
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6412.810000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3957.xml