Li Xiongfeng, Sharen Gaowa, Zhang Minjie, Zhang Lei, Liu Kejian, Wang Yu, Cheng Haidong, Hou Mingxing
Department of Gastrointestinal Surgery, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, 010059, Inner Mongolia, China.
Department of Pathology, Affiliated Hospital of Inner Mongolia Medical University & Department of Pathological Anatomy, College of Basic Medicine of Inner Mongolia Medical University, Hohhot, 010059, Inner Mongolia, China.
Heliyon. 2024 Jul 23;10(15):e35002. doi: 10.1016/j.heliyon.2024.e35002. eCollection 2024 Aug 15.
To undertake a comprehensive assay of PDCD11 expression in colorectal cancer (CRC) and its association with prognosis and immune cell infiltration (ICIN) utilizing bioinformatics tools.
The PDCD11 expression in CRC and pan-cancer was quantified through datasets from TCGA and GEO databases, and the assay was conducted through R software and the GEPIA database. Moreover, mRNA and protein expression data of PDCD11 were attained from the HPA database. It was attempted to establish protein-protein interaction networks of PDCD11 via the STRING and GeneMANIA databases. The association of PDCD11 expression with CRC staging was evaluated through R software, while its association with CRC and pan-cancer prognosis was figured out via the GEPIA database. Furthermore, the relationship of PDCD11 expression with ICIN was assayed using R software and the TIMER database. Additionally, the influences of PDCD11 knockdown on the proliferation, apoptosis, and migration of colon cancer RKO cell lines was evaluated.
PDCD11 exhibited elevated expression in CRC and various other malignancies, potentially indicating a promotive role in cancer progression. Overexpression of PDCD11 was found to correlate with attenuated overall survival in CRC and other malignancies. Moreover, PDCD11 demonstrated promising predictive capabilities for distinguishing between tumor and non-tumor tissues. The positive association of high PDCD11 expression with the infiltration of neutrophils, dendritic cells, CD8 T cells, CD4 T cells, and macrophages, as well as with the expression of immune checkpoint molecules CTLA4 and PD-1 was noteworthy. Lentivirus-mediated PDCD11 knockdown suppressed RKO cell proliferation, colony formation, and migration, while triggered apoptosis in these cells.
The outcomes unveiled the noticeable function of PDCD11 in CRC and various other malignancies, emphasizing its potential as a prognostic biomarker and therapeutic target.
利用生物信息学工具对结直肠癌(CRC)中PDCD11的表达及其与预后和免疫细胞浸润(ICIN)的关系进行全面分析。
通过来自TCGA和GEO数据库的数据集对CRC和泛癌中PDCD11的表达进行定量,并通过R软件和GEPIA数据库进行分析。此外,从HPA数据库获得PDCD11的mRNA和蛋白质表达数据。试图通过STRING和GeneMANIA数据库建立PDCD11的蛋白质-蛋白质相互作用网络。通过R软件评估PDCD11表达与CRC分期的关系,同时通过GEPIA数据库确定其与CRC和泛癌预后的关系。此外,使用R软件和TIMER数据库分析PDCD11表达与ICIN的关系。另外,评估了PDCD11敲低对结肠癌RKO细胞系增殖、凋亡和迁移的影响。
PDCD11在CRC和其他多种恶性肿瘤中表达升高,可能表明其在癌症进展中起促进作用。发现PDCD11的过表达与CRC和其他恶性肿瘤的总生存期缩短相关。此外,PDCD11在区分肿瘤组织和非肿瘤组织方面显示出有前景的预测能力。值得注意的是,高PDCD11表达与中性粒细胞、树突状细胞、CD8 T细胞、CD4 T细胞和巨噬细胞的浸润以及免疫检查点分子CTLA4和PD-1的表达呈正相关。慢病毒介导的PDCD11敲低抑制了RKO细胞的增殖、集落形成和迁移,同时引发了这些细胞的凋亡。
结果揭示了PDCD11在CRC和其他多种恶性肿瘤中的显著作用,强调了其作为预后生物标志物和治疗靶点的潜力。