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
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.