Abstract
Frequent homozygous deletions of the p16 (MTS1) gene encoding a cyclin-dependent kinase inhibitor were recently reported in various tumor cell lines including examples derived from lung cancers, but direct evidence for their occurrence in lung cancer patients has not been reported thus far. In the present study, alterations of p16 and/or p15, a p16-related cyclin-dependent kinase, were observed not only in lung cancer cell lines but also in the corresponding tumor specimens in vivo, excluding the possibility of in vitro artifacts. Interestingly, a clear specificity was also noted in terms of the affected histological subtype; i.e., only non-small cell lung cancers carried alterations (6 of 20 as compared to 0 of 20 small cell lung cancer cell lines).
Publication types
-
Comparative Study
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Base Sequence
-
Carcinoma, Non-Small-Cell Lung / genetics*
-
Carcinoma, Non-Small-Cell Lung / metabolism
-
Carcinoma, Small Cell / genetics
-
Carcinoma, Small Cell / metabolism*
-
Carrier Proteins / biosynthesis*
-
Carrier Proteins / genetics
-
Cell Cycle Proteins*
-
Cell Line
-
Cyclin-Dependent Kinase Inhibitor p15
-
Cyclin-Dependent Kinase Inhibitor p16
-
DNA Primers
-
Exons
-
Humans
-
Lung Neoplasms / genetics*
-
Lung Neoplasms / metabolism
-
Molecular Sequence Data
-
Oligonucleotides, Antisense
-
Polymerase Chain Reaction
-
Tumor Cells, Cultured
-
Tumor Suppressor Proteins*
Substances
-
CDKN2B protein, human
-
Carrier Proteins
-
Cell Cycle Proteins
-
Cyclin-Dependent Kinase Inhibitor p15
-
Cyclin-Dependent Kinase Inhibitor p16
-
DNA Primers
-
Oligonucleotides, Antisense
-
Tumor Suppressor Proteins