Jin Li, Qian Lili, Zhang Xin, Liu Ting
Cancer Center, Department of Pathology, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, Zhejiang, China.
Department of Pathology, Beijing Ditan Hospital, Capital Medical University, No. 8 Jing Shun East Street, Chaoyang District, Beijing, 100015, China.
Mol Cell Probes. 2025 Jul 10;83:102040. doi: 10.1016/j.mcp.2025.102040.
CPLX1 is a member of the complexin/Synaphin family. Studies have shown that CPLX1 is involved in tumor progression. However, the biological mechanism by which CPLX1 is involved in colorectal cancer (CRC) is unclear.
TIMER and TCGA database provided difference expression of CPLX1 mRNA in pan-cancer and CRC. We collected 90 cases of CRC and adjacent normal tissues for immunohistochemistry (IHC) and investigated CPLX1 protein expression and its correlation with clinical information. Cox regression and Kaplan-Meier were conducted to determine prognostic value of CPLX1 expression. We utilized Spearman analysis to explore the association between CPLX1 and immune cell infiltration, immune checkpoints. We utilized GSEA to investigate the biological molecular function for CPLX1 in CRC.
CPLX1 mRNA expression was elevated in several cancers, including CRC. Elevated CPLX1 protein expression was confirmed by IHC in CRC samples, and showed a positive association with T stage. The survival analysis demonstrated that CPLX1 overexpression was linked to a poorer overall survival (OS), disease-specific survival (DSS), and progress-free interval (PFI) for CRC. Time ROC analysis suggested that the survival rate of 1-year, 2-year and 3-year for OS, DSS, and PFI was above 0.5, suggesting a certain prognostic value in CRC. Cox regression considered CPLX1 expression as a good prognostic index for predicting OS, DSS, and PFI. Furthermore, CPLX1 expression was associated with immunity in CRC. Functional analysis showed that CPLX1 related genes had participation in Notch signaling pathway.
CPLX1 was a latent prognostic and diagnostic marker for CRC and may also be a potential therapeutic target.
CPLX1是复合蛋白/Synaphin家族的成员。研究表明CPLX1参与肿瘤进展。然而,CPLX1参与结直肠癌(CRC)的生物学机制尚不清楚。
TIMER和TCGA数据库提供了CPLX1 mRNA在泛癌和CRC中的差异表达。我们收集了90例CRC及癌旁正常组织进行免疫组织化学(IHC)检测,研究CPLX1蛋白表达及其与临床信息的相关性。进行Cox回归和Kaplan-Meier分析以确定CPLX1表达的预后价值。我们利用Spearman分析探索CPLX1与免疫细胞浸润、免疫检查点之间的关联。我们利用基因集富集分析(GSEA)研究CPLX1在CRC中的生物学分子功能。
CPLX1 mRNA表达在包括CRC在内的几种癌症中升高。IHC证实CRC样本中CPLX1蛋白表达升高,且与T分期呈正相关。生存分析表明,CPLX1过表达与CRC患者较差的总生存期(OS)、疾病特异性生存期(DSS)和无进展生存期(PFI)相关。时间ROC分析表明,OS、DSS和PFI的1年、2年和3年生存率均高于0.5,提示在CRC中具有一定的预后价值。Cox回归将CPLX1表达视为预测OS、DSS和PFI的良好预后指标。此外,CPLX1表达与CRC中的免疫相关。功能分析表明,CPLX1相关基因参与Notch信号通路。
CPLX1是CRC潜在的预后和诊断标志物,也可能是潜在的治疗靶点。