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Increased expression of mutant forms of p53 oncogene in primary lung cancer
R. Iggo, K. Gatter, J. Bartek, D. Lane, AL. Harris,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
1969059
Knihovny.cz E-zdroje
- MeSH
- adenokarcinom analýza genetika MeSH
- alely MeSH
- autoradiografie MeSH
- DNA nádorová analýza MeSH
- fosfoproteiny analýza genetika MeSH
- imunohistochemie MeSH
- karcinoid analýza genetika MeSH
- lidé MeSH
- lidské chromozomy, pár 17 * MeSH
- malobuněčný karcinom analýza genetika MeSH
- messenger RNA analýza MeSH
- molekulární sekvence - údaje MeSH
- mutace * MeSH
- nádorový supresorový protein p53 MeSH
- nádory plic analýza genetika MeSH
- oligonukleotidové sondy MeSH
- onkogenní proteiny analýza genetika MeSH
- polymerázová řetězová reakce MeSH
- sekvence aminokyselin MeSH
- spinocelulární karcinom analýza genetika MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Primary lung cancer samples of the major histological types were examined for expression of the tumor suppressor gene p53 by immunohistochemistry. Abnormalities in p53 expression were found in 28 of 40 carcinomas, 14 of 17 squamous tumours showing abnormal p53 expression, whereas no expression of p53 was detectable in 7 carcinoid tumours or in 10 normal lung samples. Direct evidence for homozygous expression of mutant p53 mRNA in representative carcinomas was obtained by means of an asymmetric polymerase chain reaction mRNA sequencing strategy, which allowed sequencing without any cloning step. All the mutations were G to T transversions resulting in mis-sense mutations in aminoacids highly conserved in evolution. Mutation of the p53 gene is the most frequently identified genetic change in human lung cancer; these findings suggest that simple immunohistological methods can provide strong evidence of such mutation.
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- $a Primary lung cancer samples of the major histological types were examined for expression of the tumor suppressor gene p53 by immunohistochemistry. Abnormalities in p53 expression were found in 28 of 40 carcinomas, 14 of 17 squamous tumours showing abnormal p53 expression, whereas no expression of p53 was detectable in 7 carcinoid tumours or in 10 normal lung samples. Direct evidence for homozygous expression of mutant p53 mRNA in representative carcinomas was obtained by means of an asymmetric polymerase chain reaction mRNA sequencing strategy, which allowed sequencing without any cloning step. All the mutations were G to T transversions resulting in mis-sense mutations in aminoacids highly conserved in evolution. Mutation of the p53 gene is the most frequently identified genetic change in human lung cancer; these findings suggest that simple immunohistological methods can provide strong evidence of such mutation.
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