The First School of Clinical Medicine, Nanjing University of Chinese Medicine, Nanjing, 210046, China.
Comb Chem High Throughput Screen. 2024;27(11):1642-1660. doi: 10.2174/0113862073290831240229060932.
Colorectal cancer (CRC) ranks among the leading causes of cancerrelated deaths.
This study aimed to illuminate the relationship between DPP7 (also known as DPP2) and CRC through a combination of bioinformatics and experimental methodologies.
A multi-dimensional bioinformatic analysis on DPP7 was executed, covering its expression, survival implications, clinical associations, functional roles, immune interactions, and drug sensitivities. Experimental validations involved siRNA-mediated DPP7 knockdown and various cellular assays.
Data from the Cancer Genome Atlas (TCGA) identified high DPP7 expression in solid CRC tumors, with elevated levels adversely affecting patient prognosis. A shift from the N0 to the N2 stage in CRC was associated with increased DPP7 expression. Functional insights indicated the involvement of DPP7 in cancer progression, particularly in extracellular matrix disassembly. Immunological analyses showed its association with immunosuppressive entities, and in vitro experiments in CRC cell lines underscored its oncogenic attributes.
DPP7 could serve as a CRC prognosis marker, functioning as an oncogene and representing a potential immunotherapeutic target.
结直肠癌(CRC)是癌症相关死亡的主要原因之一。
本研究旨在通过生物信息学和实验方法相结合,阐明 DPP7(也称为 DPP2)与 CRC 之间的关系。
对 DPP7 进行多维生物信息学分析,包括其表达、生存意义、临床关联、功能作用、免疫相互作用和药物敏感性。实验验证涉及 siRNA 介导的 DPP7 敲低和各种细胞测定。
癌症基因组图谱(TCGA)的数据表明,DPP7 在实体 CRC 肿瘤中高表达,高水平表达对患者预后不利。CRC 中从 N0 期到 N2 期的转变与 DPP7 表达的增加有关。功能研究表明 DPP7 参与了癌症的进展,特别是在细胞外基质的分解中。免疫分析表明其与免疫抑制实体有关,CRC 细胞系中的体外实验也强调了其致癌特性。
DPP7 可作为 CRC 的预后标志物,发挥癌基因的作用,代表潜在的免疫治疗靶点。