Department of Clinical Laboratory, Yue Bei People's Hospital, Shantou University Medical College, Shaoguan, Guangdong, P.R. China.
Liver Cancer Institute, Zhongshan Hospital, Fudan University and Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Shanghai, P.R. China.
Biosci Rep. 2020 Jul 31;40(7). doi: 10.1042/BSR20201384.
The neurotransmitter, serotonin has emerged as a tumor growth factor and immune response regulator through complex signaling pathways. Yip1 Interacting Factor Homolog B (YIF1B) is a membrane protein involved in serotonin receptor (HTR) membrane trafficking and signal transmission in neuropathy. Participation of YIF1B in serotonin-induced tumor growth and immune regulation has not been previously investigated. Data for analysis of YIF1B mRNA expression were downloaded from the website portals: The Cancer Genome Atlas (TCGA), GTEx, Cancer Cell Line Encyclopedia (CCLE) and International Cancer Genome Consortium (ICGC), including clinical and mutational information. Survival analysis included the Kaplan-Meier method for calculation of the cumulative incidence of the survival event and the log rank method for comparison of survival curves between groups. Infiltration levels of immune cells were calculated and correlated with YIF1B expression using the Spearman correlation test to evaluate significance. Further correlation analyses between YIF1B expression and mutation indicators such as tumor mutation burden (TMB), microsatellite instability (MSI), and mismatch repair (MMR) were also examined by the Spearman test. YIF1B expression was elevated in most cancer types and this high expression was indicative of poor overall survival (OS) and death-specific survival. In breast invasive carcinoma (BRCA) and liver hepatocellular carcinoma (LIHC), high YIF1B expression correlated with a poor disease-free interval (DFI), indicating a role in malignancy progression. There was a positive relationship between YIF1B expression and immune cell infiltration in several cancer types, and YIF1B also positively correlated with TMB, MSI, and methylation in some cancer types, linking its expression to possible evaluation of therapy response. The bioinformatics analyses have, therefore, established YIF1B as a good biomarker for prognostic and therapeutic evaluation.
神经递质 5-羟色胺已通过复杂的信号通路成为肿瘤生长因子和免疫反应调节剂。Yip1 相互作用因子同源物 B(YIF1B)是一种膜蛋白,参与神经病变中的 5-羟色胺受体(HTR)膜转运和信号转导。YIF1B 参与 5-羟色胺诱导的肿瘤生长和免疫调节尚未被研究过。用于分析 YIF1B mRNA 表达的数据从网站门户下载:癌症基因组图谱(TCGA)、GTEx、癌症细胞系百科全书(CCLE)和国际癌症基因组联合会(ICGC),包括临床和突变信息。生存分析包括 Kaplan-Meier 法计算生存事件的累积发生率和对数秩检验比较组间生存曲线。计算免疫细胞的浸润水平,并使用 Spearman 相关检验将其与 YIF1B 表达相关联,以评估显著性。还通过 Spearman 检验进一步研究了 YIF1B 表达与肿瘤突变负荷(TMB)、微卫星不稳定性(MSI)和错配修复(MMR)等突变指标之间的相关性。YIF1B 在大多数癌症类型中表达升高,这种高表达与总生存期(OS)和死亡特异性生存期差相关。在乳腺浸润性癌(BRCA)和肝细胞癌(LIHC)中,高 YIF1B 表达与不良无病间隔(DFI)相关,表明其在恶性进展中起作用。在几种癌症类型中,YIF1B 表达与免疫细胞浸润呈正相关,在某些癌症类型中,YIF1B 与 TMB、MSI 和甲基化呈正相关,将其表达与可能的治疗反应评估联系起来。因此,生物信息学分析将 YIF1B 确立为预后和治疗评估的良好生物标志物。