Department of General Surgery, Guangzhou Digestive Disease Center, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, Guangdong, China.
Chronic Disease Laboratory, Institutes for Life Sciences, South China University of Technology, Guangzhou, China.
J Cell Mol Med. 2020 Oct;24(20):12176-12187. doi: 10.1111/jcmm.15867. Epub 2020 Sep 14.
The Notch signalling pathway is involved in the development of several cancers, including colorectal cancer (CRC). However, whether mutations in this pathway could alter the CRC immunophenotype remains unknown. Here, we investigated the relationship between Notch signalling pathway mutations and the tumour immune microenvironment by analysing gene expression data from the GSE108989 single T cell RNA sequencing data set and The Cancer Genome Atlas (TCGA) data set. We found that Notch signalling pathway mutations were associated with an increased number of tumour-specific CD8 T cells and decreased number of inhibitory regulatory T (Treg) cells, representing an enhanced anti-tumour response in the GSE108989 data set. In TCGA data set, we also found that Notch signalling pathway mutations were associated with enrichment of genes associated with immune activation pathways and higher expressions of PDCD1, GZMB and PRF1. Although Notch signalling pathway mutations did not affect the overall survival and disease-free survival of CRC patients, they were associated with earlier disease stages and lower rates of metastasis. These results demonstrated that Notch signalling pathway mutations can enhance anti-tumour immunity in CRC, as validated by the two data sets, suggesting that they may be promising biomarkers for immune checkpoint blockade therapies for CRC patients.
Notch 信号通路参与了多种癌症的发展,包括结直肠癌(CRC)。然而,该通路中的突变是否会改变 CRC 的免疫表型尚不清楚。在这里,我们通过分析来自 GSE108989 单细胞 RNA 测序数据集和癌症基因组图谱(TCGA)数据集的基因表达数据,研究了 Notch 信号通路突变与肿瘤免疫微环境之间的关系。我们发现,Notch 信号通路突变与肿瘤特异性 CD8 T 细胞数量增加和抑制性调节性 T(Treg)细胞数量减少有关,这代表了 GSE108989 数据集中增强的抗肿瘤反应。在 TCGA 数据集中,我们还发现 Notch 信号通路突变与与免疫激活途径相关的基因富集以及 PDCD1、GZMB 和 PRF1 的高表达有关。尽管 Notch 信号通路突变不会影响 CRC 患者的总体生存率和无病生存率,但它们与早期疾病阶段和较低的转移率有关。这些结果表明,Notch 信号通路突变可以增强 CRC 中的抗肿瘤免疫,这在两个数据集都得到了验证,这表明它们可能是 CRC 患者免疫检查点阻断治疗的有前途的生物标志物。