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FCRLB高表达预示着结直肠癌患者的预后不良。

High Expression of FCRLB Predicts Poor Prognosis in Patients With Colorectal Cancer.

作者信息

Wang Xiaopeng, Lin Ruirong, Zeng Yi, Wang Yi, Wei Shenghong, Lin Zhitao, Chen Shu, Ye Zaisheng, Chen Luchuan

机构信息

Department of Gastrointestinal Surgical Oncology, Fujian Medical University Cancer Hospital, Fujian Cancer Hospital, Fuzhou, China.

出版信息

Front Genet. 2022 Jun 16;13:882307. doi: 10.3389/fgene.2022.882307. eCollection 2022.

Abstract

Mining the prognostic biomarkers of colorectal cancer (CRC) has important clinical and scientific significance. The role of Fc receptor-like B (FCRLB) in solid tumors has never been reported or studied to our knowledge, and the prognostic role of FCRLB in CRC still awaits characterization. The potential prognostic factor FCRLB was screened out through TCGA database analysis. Then, its expression and associations with clinicopathological variables were assessed in the TCGA CRC cohort. The prognostic value of FCRLB was examined with multiple methods, such as the Kaplan-Meier method, ROC curve, time-dependent ROC analysis, and prediction model nomograms. Then, functional enrichment and annotation among the high and low FCRLB groups were achieved utilizing GO and KEGG analyses and GSEA. Fresh CRC tissue samples obtained clinically were used for the preparation of the tissue microarray and for further validation. FCRLB was highly expressed in CRC tissues compared to normal tissues. Moreover, over-expression of FCRLB correlated with higher CEA levels, advanced T stage, N stage, M stage, AJCC stage, lymphatic invasion, perineural invasion, and incomplete resection (R1 and R2 resection). In addition, high expression of FCRLB was closely correlated to less favorable OS, DSS, and PFI. The analysis of CRC tissue microarray further confirmed the conclusion drawn from the TCGA data analysis. FCRLB is notably up-regulated in CRC tissues and may serve as a potential biomarker of CRC.

摘要

挖掘结直肠癌(CRC)的预后生物标志物具有重要的临床和科学意义。据我们所知,Fc受体样B(FCRLB)在实体瘤中的作用从未被报道或研究过,FCRLB在CRC中的预后作用仍有待明确。通过TCGA数据库分析筛选出潜在的预后因子FCRLB。然后,在TCGA CRC队列中评估其表达以及与临床病理变量的相关性。采用多种方法检验FCRLB的预后价值,如Kaplan-Meier法、ROC曲线、时间依赖性ROC分析和预测模型列线图。然后,利用GO和KEGG分析以及GSEA实现高FCRLB组和低FCRLB组之间的功能富集和注释。临床上获取的新鲜CRC组织样本用于制备组织芯片并进行进一步验证。与正常组织相比,FCRLB在CRC组织中高表达。此外,FCRLB的过表达与较高的CEA水平、晚期T分期、N分期、M分期、AJCC分期、淋巴浸润、神经周围浸润和不完全切除(R1和R2切除)相关。此外,FCRLB的高表达与较差的总生存期(OS)、无病生存期(DSS)和无进展生存期(PFI)密切相关。CRC组织芯片分析进一步证实了从TCGA数据分析得出的结论。FCRLB在CRC组织中显著上调,可能作为CRC的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e9a/9244534/a99ee0250692/fgene-13-882307-g001.jpg

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