Shao Yuyang, Shi Tongguo, Guo Lingchuan, Chen Weichang
Department of Gastroenterology, First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Jiangsu Institute of Clinical Immunology, Jiangsu Key Laboratory of Gastrointestinal Tumor Immunology, First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2024 May;40(5):435-442.
Objective To elucidate the expression characteristics and clinical significance of B7 homolog 3(B7-H3) in colorectal cancer (CRC) and to explore its associations with tumor glycolysis and immune cell infiltration in the tumor microenvironment. Methods The transcriptomic and clinicopathological data of CRC were obtained from the TCGA database and analyzed to determine the expression and clinical relevance of B7-H3. Correlations between glycolysis-related genes and B7-H3 expression were assessed based on TCGA data. The associations between B7-H3 expression and the infiltration of 22 types of immune cells were analyzed using the CIBERSORT algorithm. Immunohistochemical staining was used to verify the results of database analysis in surgical specimens and adjacent normal tissue specimens of 51 CRC patients.Results B7-H3 was significantly upregulated in CRC tissues and demonstrated strong correlations with tumor invasion depth, advanced TNM stage, and poor prognosis. Additionally, B7-H3 expression was closely associated with the upregulation of glycolysis-related genes in CRC. Immune cell infiltration analysis revealed that a total of 16 types of immune cells were significantly correlated with B7-H3 expression. Furthermore, an inverse relationship between B7-H3 expression and CD8T cell infiltration was identified at the transcriptional level but not at the protein level. Conclusion B7-H3 is highly expressed in CRC tissues and is significantly correlated with disease progression and poor prognosis. Furthermore, the association of B7-H3 expression with glycolysis-related genes and immune cell infiltration suggests a pivotal role of B7-H3 in the regulation of tumor glycolysis and cancer immunity.
目的 阐明B7同源物3(B7-H3)在结直肠癌(CRC)中的表达特征及临床意义,并探讨其与肿瘤糖酵解及肿瘤微环境中免疫细胞浸润的关系。方法 从TCGA数据库获取CRC的转录组和临床病理数据,分析确定B7-H3的表达及临床相关性。基于TCGA数据评估糖酵解相关基因与B7-H3表达的相关性。使用CIBERSORT算法分析B7-H3表达与22种免疫细胞浸润的关系。采用免疫组化染色验证51例CRC患者手术标本及癌旁正常组织标本数据库分析结果。结果 B7-H3在CRC组织中显著上调,与肿瘤浸润深度、TNM分期及预后不良密切相关。此外,B7-H3表达与CRC中糖酵解相关基因的上调密切相关。免疫细胞浸润分析显示,共有16种免疫细胞与B7-H3表达显著相关。此外,在转录水平发现B7-H3表达与CD8 + T细胞浸润呈负相关,但在蛋白水平未发现此现象。结论 B7-H3在CRC组织中高表达,与疾病进展及预后不良显著相关。此外,B7-H3表达与糖酵解相关基因及免疫细胞浸润的关系表明,B7-H3在肿瘤糖酵解和癌症免疫调节中起关键作用。