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Specific T-cell immunity against Ki-ras peptides in patients with pancreatic and colorectal cancers
Mutations of codon 12 in the Ki-ras gene are frequently found in pancreatic and colorectal cancers. It has been demonstrated that human T-cells have the potential to recognise tumours expressing mutated ras-derived peptides. However, it remains unclear whether T-cells from a given individual can rec...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2003
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2377177/ https://www.ncbi.nlm.nih.gov/pubmed/12592366 http://dx.doi.org/10.1038/sj.bjc.6600697 |
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author | Shono, Y Tanimura, H Iwahashi, M Tsunoda, T Tani, M Tanaka, H Matsuda, K Yamaue, H |
author_facet | Shono, Y Tanimura, H Iwahashi, M Tsunoda, T Tani, M Tanaka, H Matsuda, K Yamaue, H |
author_sort | Shono, Y |
collection | PubMed |
description | Mutations of codon 12 in the Ki-ras gene are frequently found in pancreatic and colorectal cancers. It has been demonstrated that human T-cells have the potential to recognise tumours expressing mutated ras-derived peptides. However, it remains unclear whether T-cells from a given individual can recognise the mutant peptides, which are expressed in that individual's tumour tissues. Mutations of the Ki-ras oncogene were analysed by the mutant-allele-specific amplification (MASA) method in pancreatic and colorectal tumour tissues, and T-cell responses against mutated Ki-ras-derived peptides were measured by [(3)H]thymidine incorporation and IFN-γ production assays. Specific T-cell responses against Ki-ras-products were found in cancer patients, whereas no immune response was observed in normal individuals (P<0.01). Six of the eight pancreatic cancer patients (75%) and nine of 26 colorectal cancer patients (35%) had T-cell responses to mutated Ki-ras-derived-peptides. T-cell response in a given individual cannot recognise the same mutated ras peptide, which is expressed in that individual's tumour tissues. However, pancreatic and colorectal cancer patients have T-cell immunity against Ki-ras-peptides, and this provides potential target for cancer immunotherapy. |
format | Text |
id | pubmed-2377177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23771772009-09-10 Specific T-cell immunity against Ki-ras peptides in patients with pancreatic and colorectal cancers Shono, Y Tanimura, H Iwahashi, M Tsunoda, T Tani, M Tanaka, H Matsuda, K Yamaue, H Br J Cancer Molecular and Cellular Pathology Mutations of codon 12 in the Ki-ras gene are frequently found in pancreatic and colorectal cancers. It has been demonstrated that human T-cells have the potential to recognise tumours expressing mutated ras-derived peptides. However, it remains unclear whether T-cells from a given individual can recognise the mutant peptides, which are expressed in that individual's tumour tissues. Mutations of the Ki-ras oncogene were analysed by the mutant-allele-specific amplification (MASA) method in pancreatic and colorectal tumour tissues, and T-cell responses against mutated Ki-ras-derived peptides were measured by [(3)H]thymidine incorporation and IFN-γ production assays. Specific T-cell responses against Ki-ras-products were found in cancer patients, whereas no immune response was observed in normal individuals (P<0.01). Six of the eight pancreatic cancer patients (75%) and nine of 26 colorectal cancer patients (35%) had T-cell responses to mutated Ki-ras-derived-peptides. T-cell response in a given individual cannot recognise the same mutated ras peptide, which is expressed in that individual's tumour tissues. However, pancreatic and colorectal cancer patients have T-cell immunity against Ki-ras-peptides, and this provides potential target for cancer immunotherapy. Nature Publishing Group 2003-02-24 2003-02-18 /pmc/articles/PMC2377177/ /pubmed/12592366 http://dx.doi.org/10.1038/sj.bjc.6600697 Text en Copyright © 2003 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Molecular and Cellular Pathology Shono, Y Tanimura, H Iwahashi, M Tsunoda, T Tani, M Tanaka, H Matsuda, K Yamaue, H Specific T-cell immunity against Ki-ras peptides in patients with pancreatic and colorectal cancers |
title | Specific T-cell immunity against Ki-ras peptides in patients with pancreatic and colorectal cancers |
title_full | Specific T-cell immunity against Ki-ras peptides in patients with pancreatic and colorectal cancers |
title_fullStr | Specific T-cell immunity against Ki-ras peptides in patients with pancreatic and colorectal cancers |
title_full_unstemmed | Specific T-cell immunity against Ki-ras peptides in patients with pancreatic and colorectal cancers |
title_short | Specific T-cell immunity against Ki-ras peptides in patients with pancreatic and colorectal cancers |
title_sort | specific t-cell immunity against ki-ras peptides in patients with pancreatic and colorectal cancers |
topic | Molecular and Cellular Pathology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2377177/ https://www.ncbi.nlm.nih.gov/pubmed/12592366 http://dx.doi.org/10.1038/sj.bjc.6600697 |
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