COMPARATIVE-ANALYSIS OF P16 CDKN2, P53 AND RAS GENE ALTERATIONS IN HUMAN NON-SMALL-CELL LUNG CANCERS, WITH AND WITHOUT ASSOCIATED PULMONARYASBESTOSIS/

Citation
I. Hayashi et al., COMPARATIVE-ANALYSIS OF P16 CDKN2, P53 AND RAS GENE ALTERATIONS IN HUMAN NON-SMALL-CELL LUNG CANCERS, WITH AND WITHOUT ASSOCIATED PULMONARYASBESTOSIS/, International journal of oncology, 8(1), 1996, pp. 85-90
Citations number
39
Categorie Soggetti
Oncology
ISSN journal
10196439
Volume
8
Issue
1
Year of publication
1996
Pages
85 - 90
Database
ISI
SICI code
1019-6439(1996)8:1<85:COPCPA>2.0.ZU;2-E
Abstract
To investigate genetic abnormalities in human non-small cell lung carc inomas (NSCLC) associated with pulmonary asbestosis as compared with n ou-asbestos linked lung cancers, twenty-nine primary non-small cell lu ng carcinomas (NSCLC) were examined for genetic abnormalities of p16/C DKN2, p53 and ras genes by single-strand conformation polymorphism ana lysis of polymerase chain reaction products (PCR-SSCP) and direct sequ encing. Ten specimens were obtained from autopsies in which concurrent pulmonary asbestosis was present, while 19 samples were surgical spec imens from asbestosis-free patients. K-ras mutations were detected in 10% each of the cancers from both asbestosis and non-asbestosis cases. p16/CDKN2 deletions or mutations and p53 aberrations were demonstrate d in 20% and 10% of tumors from asbestosis cases, whereas, 32% and 21% of the cancers, respectively, from asbestosis-free patients were posi tive. In conclusion, it is suggested that the enhancement of neoplasia in the lung by asbestos is not dependent on suppression of p16/CDKN2 and p53 or ras activation and therefore, that asbestosis may activate alternate tumorigenic pathways in the development of NSCLC.