Hu Yue, Ding Jie, Wu Chengjiang, Gao Hong, Ge Meiling, Shao Qixiang, Liu Yanhong, Ye Qing
Biobank of Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing, China.
Department of Clinical Laboratory, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Front Oncol. 2022 Jul 22;12:845765. doi: 10.3389/fonc.2022.845765. eCollection 2022.
Growing evidence suggests that colorectal cancer (CRC) should be considered a heterogeneous disease. The right side (RCC) and left side (LCC) colorectal cancer have different clinical characteristics and immune landscapes. The aim of this study was to analyze differential expression and prognostic correlation of immune-related factors between RCC and LCC.
The gene expression profile and clinical characteristics of CRC patients were retrieved from The Cancer Genome Atlas data portal (n=525). Using a deconvolution algorithm, immune cell infiltration in RCC and LCC based on the RNA-seq data was analyzed. Differentially expressed genes (DEGs) were obtained by performing differential gene expression analysis. Immune-related DEGs were derived by the intersection with immune-related factors downloaded from the IMMPORT database. To further validate the findings, we applied immunohistochemical (IHC) staining of a CRC tissue microarray (TMA). The distribution of immune cells in RCC and LCC and changes in the expression of immune molecules on their membranes were verified. The expression levels of circulating cytokines were measured by flow cytometry to detect the cytokines secreted by immune cells in RCC and LCC. Furthermore, to reveal the prognostic value of differential immune factors on RCC and LCC patients, survival analysis based on mRNA levels using TCGA cohort and survival analysis using protein levels was performed using our CRC patients.
The infiltration of immune cells differed between RCC and LCC, the infiltration degree of macrophages M0 was significantly higher in LCC, while the infiltration degree of differentiated macrophages M1 and M2, CD4+ T and CD8+ T cells was significantly higher in RCC. The expression of related molecules by immune cells also differed between RCC and LCC. The expression of 7 genes in RCC was higher than that in LCC, which were CCR5, CD209, CD8A, HCK, HLA-DPB1, HLA-DQA1, HLA-DRA, respectively. Meanwhile, the expression of 2 genes in LCC was higher than in RCC, which were IL-34 and PROCR. Patients with RCC having high expression of HLA-DQA1 mRNA or proteins had better survival and LCC patients with high expression of IL 34 mRNA or protein had better survival.
In this study, we comprehensively compared differences in immune cells and regulating factors between left and right colorectal cancer. Different expression patterns and their effects on survival were identified. The analysis of immune-related factors may provide a theoretical basis for precise immunotherapy of RCC and LCC.
越来越多的证据表明,结直肠癌(CRC)应被视为一种异质性疾病。右侧结直肠癌(RCC)和左侧结直肠癌(LCC)具有不同的临床特征和免疫格局。本研究旨在分析RCC和LCC之间免疫相关因子的差异表达及其与预后的相关性。
从癌症基因组图谱数据门户检索CRC患者的基因表达谱和临床特征(n = 525)。使用反卷积算法,基于RNA测序数据分析RCC和LCC中的免疫细胞浸润情况。通过进行差异基因表达分析获得差异表达基因(DEG)。通过与从IMMPORT数据库下载的免疫相关因子进行交集运算,得出免疫相关DEG。为进一步验证研究结果,我们对CRC组织芯片(TMA)进行了免疫组织化学(IHC)染色。验证了RCC和LCC中免疫细胞的分布以及它们细胞膜上免疫分子表达的变化。通过流式细胞术测量循环细胞因子的表达水平,以检测RCC和LCC中免疫细胞分泌的细胞因子。此外,为揭示差异免疫因子对RCC和LCC患者的预后价值,使用我们的CRC患者基于TCGA队列的mRNA水平进行生存分析以及基于蛋白质水平进行生存分析。
RCC和LCC中免疫细胞的浸润情况不同,LCC中M0巨噬细胞的浸润程度显著更高,而RCC中分化型M1和M2巨噬细胞、CD4 + T细胞和CD8 + T细胞的浸润程度显著更高。RCC和LCC中免疫细胞相关分子的表达也存在差异。RCC中有7个基因的表达高于LCC,分别为CCR5、CD209、CD8A、HCK、HLA - DPB1、HLA - DQA1、HLA - DRA。同时,LCC中有2个基因的表达高于RCC,分别为IL - 34和PROCR。HLA - DQA1 mRNA或蛋白高表达的RCC患者生存情况较好,IL - 34 mRNA或蛋白高表达的LCC患者生存情况较好。
在本研究中,我们全面比较了左、右半结肠癌之间免疫细胞和调节因子的差异。确定了不同的表达模式及其对生存的影响。免疫相关因子的分析可能为RCC和LCC的精准免疫治疗提供理论依据。