Topographic analysis of K-ras mutations in histologically normal lung tissues and tumours of lung cancer patients

Citation
P. Keohavong et al., Topographic analysis of K-ras mutations in histologically normal lung tissues and tumours of lung cancer patients, BR J CANC, 85(2), 2001, pp. 235-241
Citations number
42
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
BRITISH JOURNAL OF CANCER
ISSN journal
00070920 → ACNP
Volume
85
Issue
2
Year of publication
2001
Pages
235 - 241
Database
ISI
SICI code
0007-0920(20010720)85:2<235:TAOKMI>2.0.ZU;2-V
Abstract
Mutations in the K-ras gene are very common in lung tumours and are implica ted in the development of lung cancer, but the timing of their occurrence r emains poorly understood. We investigated K-ras mutations in cell samples m icrodissected by laser capture microscopy at multiple sites from lung tissu e sections representing tumour tissue and matched histologically normal tis sue obtained from 48 lung cancer patients. K-ras mutations were detected in cell samples from 10 of 38 (26.3%) lung adenocarcinomas and in none of the histologically normal or tumour cell samples taken from 10 lung squamous c ell carcinomas. Of the K-ras mutation-positive adenocarcinomas, in 4 cases a mutation was found in only the tumour tissue, in 1 case a mutation was fo und only in the histologically normal tissue, and in 5 cases mutations were found in both the tumour tissue and histologically normal tissue. Among th ese 5 cases, 2 had identical mutations in both the tumour tissue and histol ogically normal tissue, 2 had 1 mutation in the tumour tissue and 2 mutatio ns in the histologically normal tissue, 1 of which was identical to the mut ation found in the tumour, and 1 case had 2 codon 12 mutations in tumour ti ssue and 2 mutations, in codons 9 and 11, in histologically normal tissue. These results showed that K-ras mutations are frequent in histologically no rmal cells taken from outside lung adenocarcinomas and suggest that some of these mutations may represent early events which could pave the way of lun g carcinogenesis. (C) 2001 Cancer Research Campaign.