Cargando…

Specific Growth Inhibition of Small‐cell Lung Cancer Cells by Adenovirus Vector Expressing Antisense c‐kit Transcripts

Antisense methods to control aberrant gene expression have been investigated as therapeutic strategies. A proto‐oncogene c‐kit, which encodes a transmembrane tyrosine kinase, is overexpressed in some malignancies, including small‐cell lung cancer (SCLC), and is thought to be involved in their pathog...

Descripción completa

Detalles Bibliográficos
Autores principales: Yamanishi, Yuji, Maeda, Hiroyuki, Hiyama, Keiko, Ishioka, Shinichi, Yamakido, Michio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921119/
https://www.ncbi.nlm.nih.gov/pubmed/8641992
http://dx.doi.org/10.1111/j.1349-7006.1996.tb00256.x
_version_ 1783317942859988992
author Yamanishi, Yuji
Maeda, Hiroyuki
Hiyama, Keiko
Ishioka, Shinichi
Yamakido, Michio
author_facet Yamanishi, Yuji
Maeda, Hiroyuki
Hiyama, Keiko
Ishioka, Shinichi
Yamakido, Michio
author_sort Yamanishi, Yuji
collection PubMed
description Antisense methods to control aberrant gene expression have been investigated as therapeutic strategies. A proto‐oncogene c‐kit, which encodes a transmembrane tyrosine kinase, is overexpressed in some malignancies, including small‐cell lung cancer (SCLC), and is thought to be involved in their pathogenesis. To test the feasibility of using adenovirus vectors for antisense strategies and to target c‐kit in SCLC therapy, we constructed replication‐deficient recombinant adenovirus vectors which express fragments of c‐kit transcripts in antisense (Ad.kitAS) or sense orientation (Ad.kitS: control). In vitro infection of SBC‐1 cells, which are c‐Kit protein‐producing SCLC cells, by these vectors resulted in the expression of artificial c‐kit transcripts. The Ad.kitAS‐infected SBC‐1 cells showed reductions in the amount of c‐Kit protein. As expected, at 10 days after infection (1 multiplicity of infection), Ad.kitAS‐infected SBC‐1 cells showed approximately 40% growth inhibition compared to uninfected or Ad.kitS‐infected cells in vitro. Such a significant growth inhibition by Ad.kitAS was not induced in SBC‐5 cells, which are SCLC cells producing no c‐Kit protein. These results demonstrate the usefulness of adenovirus vectors in antisense strategies, and the feasibility of targeting c‐kit in the therapy of c‐Kit‐producing SCLC.
format Online
Article
Text
id pubmed-5921119
institution National Center for Biotechnology Information
language English
publishDate 1996
publisher Blackwell Publishing Ltd
record_format MEDLINE/PubMed
spelling pubmed-59211192018-05-11 Specific Growth Inhibition of Small‐cell Lung Cancer Cells by Adenovirus Vector Expressing Antisense c‐kit Transcripts Yamanishi, Yuji Maeda, Hiroyuki Hiyama, Keiko Ishioka, Shinichi Yamakido, Michio Jpn J Cancer Res Article Antisense methods to control aberrant gene expression have been investigated as therapeutic strategies. A proto‐oncogene c‐kit, which encodes a transmembrane tyrosine kinase, is overexpressed in some malignancies, including small‐cell lung cancer (SCLC), and is thought to be involved in their pathogenesis. To test the feasibility of using adenovirus vectors for antisense strategies and to target c‐kit in SCLC therapy, we constructed replication‐deficient recombinant adenovirus vectors which express fragments of c‐kit transcripts in antisense (Ad.kitAS) or sense orientation (Ad.kitS: control). In vitro infection of SBC‐1 cells, which are c‐Kit protein‐producing SCLC cells, by these vectors resulted in the expression of artificial c‐kit transcripts. The Ad.kitAS‐infected SBC‐1 cells showed reductions in the amount of c‐Kit protein. As expected, at 10 days after infection (1 multiplicity of infection), Ad.kitAS‐infected SBC‐1 cells showed approximately 40% growth inhibition compared to uninfected or Ad.kitS‐infected cells in vitro. Such a significant growth inhibition by Ad.kitAS was not induced in SBC‐5 cells, which are SCLC cells producing no c‐Kit protein. These results demonstrate the usefulness of adenovirus vectors in antisense strategies, and the feasibility of targeting c‐kit in the therapy of c‐Kit‐producing SCLC. Blackwell Publishing Ltd 1996-05 /pmc/articles/PMC5921119/ /pubmed/8641992 http://dx.doi.org/10.1111/j.1349-7006.1996.tb00256.x Text en
spellingShingle Article
Yamanishi, Yuji
Maeda, Hiroyuki
Hiyama, Keiko
Ishioka, Shinichi
Yamakido, Michio
Specific Growth Inhibition of Small‐cell Lung Cancer Cells by Adenovirus Vector Expressing Antisense c‐kit Transcripts
title Specific Growth Inhibition of Small‐cell Lung Cancer Cells by Adenovirus Vector Expressing Antisense c‐kit Transcripts
title_full Specific Growth Inhibition of Small‐cell Lung Cancer Cells by Adenovirus Vector Expressing Antisense c‐kit Transcripts
title_fullStr Specific Growth Inhibition of Small‐cell Lung Cancer Cells by Adenovirus Vector Expressing Antisense c‐kit Transcripts
title_full_unstemmed Specific Growth Inhibition of Small‐cell Lung Cancer Cells by Adenovirus Vector Expressing Antisense c‐kit Transcripts
title_short Specific Growth Inhibition of Small‐cell Lung Cancer Cells by Adenovirus Vector Expressing Antisense c‐kit Transcripts
title_sort specific growth inhibition of small‐cell lung cancer cells by adenovirus vector expressing antisense c‐kit transcripts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921119/
https://www.ncbi.nlm.nih.gov/pubmed/8641992
http://dx.doi.org/10.1111/j.1349-7006.1996.tb00256.x
work_keys_str_mv AT yamanishiyuji specificgrowthinhibitionofsmallcelllungcancercellsbyadenovirusvectorexpressingantisenseckittranscripts
AT maedahiroyuki specificgrowthinhibitionofsmallcelllungcancercellsbyadenovirusvectorexpressingantisenseckittranscripts
AT hiyamakeiko specificgrowthinhibitionofsmallcelllungcancercellsbyadenovirusvectorexpressingantisenseckittranscripts
AT ishiokashinichi specificgrowthinhibitionofsmallcelllungcancercellsbyadenovirusvectorexpressingantisenseckittranscripts
AT yamakidomichio specificgrowthinhibitionofsmallcelllungcancercellsbyadenovirusvectorexpressingantisenseckittranscripts