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Absence of Activating Mutations in the Transmembrane Domain of the c‐erbB‐2 Proto‐oncogene in Human Lung Cancer
The rat neu gene is known to be activated by a point mutation in its predicted transmembrane domain. Overexpression of the human homologue of neu, the c‐erbB‐2 gene, in human lung cancer has been reported, and a similar activating point mutation has been suggested. Therefore, we tested for possible...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1992
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918750/ https://www.ncbi.nlm.nih.gov/pubmed/1483946 http://dx.doi.org/10.1111/j.1349-7006.1992.tb02762.x |
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author | Sachse, Richard Murakami, Yoshinori Shiraishi, Masahiko Hayashi, Kenshi Sekiya, Takao |
author_facet | Sachse, Richard Murakami, Yoshinori Shiraishi, Masahiko Hayashi, Kenshi Sekiya, Takao |
author_sort | Sachse, Richard |
collection | PubMed |
description | The rat neu gene is known to be activated by a point mutation in its predicted transmembrane domain. Overexpression of the human homologue of neu, the c‐erbB‐2 gene, in human lung cancer has been reported, and a similar activating point mutation has been suggested. Therefore, we tested for possible aberrations of the c‐erbB‐2 gene in the region of the transmembrane domain in surgical specimens of human primary lung cancer from 190 patients, and also examined 24 metastases and 26 specimens of noncancerous portions of the lung of the same patients. Single‐strand conformation polymorphism analysis of polymerase chain reaction products revealed no point mutations in the target domain in any of these specimens. |
format | Online Article Text |
id | pubmed-5918750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1992 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59187502018-05-11 Absence of Activating Mutations in the Transmembrane Domain of the c‐erbB‐2 Proto‐oncogene in Human Lung Cancer Sachse, Richard Murakami, Yoshinori Shiraishi, Masahiko Hayashi, Kenshi Sekiya, Takao Jpn J Cancer Res Article The rat neu gene is known to be activated by a point mutation in its predicted transmembrane domain. Overexpression of the human homologue of neu, the c‐erbB‐2 gene, in human lung cancer has been reported, and a similar activating point mutation has been suggested. Therefore, we tested for possible aberrations of the c‐erbB‐2 gene in the region of the transmembrane domain in surgical specimens of human primary lung cancer from 190 patients, and also examined 24 metastases and 26 specimens of noncancerous portions of the lung of the same patients. Single‐strand conformation polymorphism analysis of polymerase chain reaction products revealed no point mutations in the target domain in any of these specimens. Blackwell Publishing Ltd 1992-12 /pmc/articles/PMC5918750/ /pubmed/1483946 http://dx.doi.org/10.1111/j.1349-7006.1992.tb02762.x Text en |
spellingShingle | Article Sachse, Richard Murakami, Yoshinori Shiraishi, Masahiko Hayashi, Kenshi Sekiya, Takao Absence of Activating Mutations in the Transmembrane Domain of the c‐erbB‐2 Proto‐oncogene in Human Lung Cancer |
title | Absence of Activating Mutations in the Transmembrane Domain of the c‐erbB‐2 Proto‐oncogene in Human Lung Cancer |
title_full | Absence of Activating Mutations in the Transmembrane Domain of the c‐erbB‐2 Proto‐oncogene in Human Lung Cancer |
title_fullStr | Absence of Activating Mutations in the Transmembrane Domain of the c‐erbB‐2 Proto‐oncogene in Human Lung Cancer |
title_full_unstemmed | Absence of Activating Mutations in the Transmembrane Domain of the c‐erbB‐2 Proto‐oncogene in Human Lung Cancer |
title_short | Absence of Activating Mutations in the Transmembrane Domain of the c‐erbB‐2 Proto‐oncogene in Human Lung Cancer |
title_sort | absence of activating mutations in the transmembrane domain of the c‐erbb‐2 proto‐oncogene in human lung cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918750/ https://www.ncbi.nlm.nih.gov/pubmed/1483946 http://dx.doi.org/10.1111/j.1349-7006.1992.tb02762.x |
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