Shono Y, Tanimura H, Iwahashi M, Tsunoda T, Tani M, Tanaka H, Matsuda K, Yamaue H
Second Department of Surgery, Wakayama Medical University, School of Medicine, Japan.
Br J Cancer. 2003 Feb 24;88(4):530-6. doi: 10.1038/sj.bjc.6600697.
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-gamma 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.
Ki-ras基因第12位密码子的突变在胰腺癌和结直肠癌中很常见。已经证明,人类T细胞有识别表达突变ras衍生肽的肿瘤的潜力。然而,尚不清楚来自特定个体的T细胞是否能识别在该个体肿瘤组织中表达的突变肽。通过突变等位基因特异性扩增(MASA)方法分析胰腺癌和结直肠癌组织中Ki-ras癌基因的突变,并通过[³H]胸腺嘧啶核苷掺入和IFN-γ产生试验测量针对突变的Ki-ras衍生肽的T细胞反应。在癌症患者中发现了针对Ki-ras产物的特异性T细胞反应,而在正常个体中未观察到免疫反应(P<0.01)。8例胰腺癌患者中有6例(75%)和26例结直肠癌患者中有9例(35%)对突变的Ki-ras衍生肽有T细胞反应。特定个体的T细胞反应无法识别在该个体肿瘤组织中表达的相同突变ras肽。然而,胰腺癌和结直肠癌患者对Ki-ras肽具有T细胞免疫,这为癌症免疫治疗提供了潜在靶点。