Expression of apoptosome pathway-related transcripts in non-small cell lung cancer
Language English Country Germany Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
16231180
PubMed Central
PMC12161016
DOI
10.1007/s00432-005-0048-6
Knihovny.cz E-resources
- MeSH
- Actins metabolism MeSH
- Apoptosis * genetics MeSH
- Adult MeSH
- Down-Regulation MeSH
- Apoptotic Protease-Activating Factor 1 MeSH
- Transcription, Genetic * MeSH
- Intracellular Signaling Peptides and Proteins genetics metabolism MeSH
- Caspase 3 MeSH
- Caspase 6 MeSH
- Caspase 7 MeSH
- Caspase 9 MeSH
- Caspases genetics metabolism MeSH
- Middle Aged MeSH
- Humans MeSH
- RNA, Messenger metabolism MeSH
- Mitochondrial Proteins genetics metabolism MeSH
- Biomarkers, Tumor genetics metabolism MeSH
- Lung Neoplasms genetics metabolism MeSH
- Carcinoma, Non-Small-Cell Lung genetics metabolism MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Enzyme Precursors metabolism MeSH
- Apoptosis Regulatory Proteins MeSH
- Proteins genetics metabolism MeSH
- Gene Expression Regulation, Neoplastic MeSH
- Aged MeSH
- Up-Regulation MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Actins MeSH
- APAF1 protein, human MeSH Browser
- CASP3 protein, human MeSH Browser
- CASP7 protein, human MeSH Browser
- CASP9 protein, human MeSH Browser
- DIABLO protein, human MeSH Browser
- Apoptotic Protease-Activating Factor 1 MeSH
- Intracellular Signaling Peptides and Proteins MeSH
- Caspase 3 MeSH
- Caspase 6 MeSH
- Caspase 7 MeSH
- Caspase 9 MeSH
- Caspases MeSH
- RNA, Messenger MeSH
- Mitochondrial Proteins MeSH
- Biomarkers, Tumor MeSH
- Enzyme Precursors MeSH
- Apoptosis Regulatory Proteins MeSH
- Proteins MeSH
PURPOSE: Tumour cells killing by cytotoxic therapies largely depends on triggering the intrinsic apoptosome-mediated caspase activation pathway but it had never been evaluated whether the expression of transcripts encoding the core components of apoptosome pathway is altered in non-small cell lung carcinoma (NSCLC). METHODS: We investigated the expression status of several apoptosome pathway-related transcripts including Apaf-1, procaspase-9, -3, -6, -7 and Smac in tumour and lung tissue samples from 65 surgically treated NSCLC patients and in 10 NSCLC cell lines with using real time RT-PCR. RESULTS: NSCLC tissues and cell lines showed significantly increased expression of procaspase-9, -3, -6 and Smac mRNAs as compared to the lungs and expression of these transcripts was simultaneously upregulated in a subset of NSCLCs belonging to different histopathological type, grade and stage categories. The expression of procaspase-7 mRNA in NSCLC tissues and cell lines and lungs was not significantly different. By contrast, the expression of Apaf-1 mRNA was frequently downregulated in the tumours as compared to matched lungs. Nevertheless, the examined NSCLC cell lines showed significantly higher expression of Apaf-1 mRNA than the lungs. The expression of Apaf-1, procaspase-9 and -6 mRNAs was higher in lung adenocarcinomas as compared to squamous cell lung carcinomas but the expression levels of the studied apoptosome pathway-related transcripts in the tumours were independent of tumour's grade and stage. CONCLUSIONS: The results of the present study suggest that there is a subgroup of NSCLCs, which may be intrinsically primed for apoptosis through upregulated expression of transcripts encoding the apoptosome pathway components.
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