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Lung cancer: intragenic ERBB2 kinase mutations in tumours.

Authors :
Stephens P
Hunter C
Bignell G
Edkins S
Davies H
Teague J
Stevens C
O'Meara S
Smith R
Parker A
Barthorpe A
Blow M
Brackenbury L
Butler A
Clarke O
Cole J
Dicks E
Dike A
Drozd A
Edwards K
Forbes S
Foster R
Gray K
Greenman C
Halliday K
Hills K
Kosmidou V
Lugg R
Menzies A
Perry J
Petty R
Raine K
Ratford L
Shepherd R
Small A
Stephens Y
Tofts C
Varian J
West S
Widaa S
Yates A
Brasseur F
Cooper CS
Flanagan AM
Knowles M
Leung SY
Louis DN
Looijenga LH
Malkowicz B
Pierotti MA
Teh B
Chenevix-Trench G
Weber BL
Yuen ST
Harris G
Goldstraw P
Nicholson AG
Futreal PA
Wooster R
Stratton MR
Source :
Nature [Nature] 2004 Sep 30; Vol. 431 (7008), pp. 525-6.
Publication Year :
2004

Abstract

The protein-kinase family is the most frequently mutated gene family found in human cancer and faulty kinase enzymes are being investigated as promising targets for the design of antitumour therapies. We have sequenced the gene encoding the transmembrane protein tyrosine kinase ERBB2 (also known as HER2 or Neu) from 120 primary lung tumours and identified 4% that have mutations within the kinase domain; in the adenocarcinoma subtype of lung cancer, 10% of cases had mutations. ERBB2 inhibitors, which have so far proved to be ineffective in treating lung cancer, should now be clinically re-evaluated in the specific subset of patients with lung cancer whose tumours carry ERBB2 mutations.

Details

Language :
English
ISSN :
1476-4687
Volume :
431
Issue :
7008
Database :
MEDLINE
Journal :
Nature
Publication Type :
Academic Journal
Accession number :
15457249
Full Text :
https://doi.org/10.1038/431525b