Department of Urology, The Second Affiliated Hospital of Shantou University Medical College, Shantou, 515041, Guangdong Province, China.
The Breast Center, Cancer Hospital of Shantou University Medical College, Shantou, 515041, Guangdong Province, China.
BMC Genom Data. 2022 Aug 9;23(1):63. doi: 10.1186/s12863-022-01070-w.
It has been previously demonstrated that hyaluronan (HA) potentially regulates the initiation and propagation of bladder cancer (BLCA). HYAL3 encodes hyaluronidase and is a potential therapeutic target for BLCA. We aimed to explore the role that HYAL3 plays in BLCA pathogenesis.
HYAL3 expression in BLCA specimens was analyzed using The Cancer Genome Atlas (TCGA) database and the Gene Expression Omnibus (GEO) cohort as well as confirmed in cell lines and The Human Protein Atlas. Then, associations between HYAL3 expression and clinicopathological data were analyzed using survival curves and receiver-operating characteristic (ROC) curves. The functions of HYAL3 were further dissected using Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis and the protein-protein interaction network. Finally, we harnessed the Tumor IMmune Estimation Resource and Gene Expression Profiling Interactive Analysis to obtain correlations between HYAL3 expression, infiltrating immunocytes, and the corresponding immune marker sets.
HYAL3 expression varied greatly between many types of cancers. In addition, a higher HYAL3 expression level predicted a poor overall survival (OS) in both TCGA-BLCA and GEO gene chips (P < 0.05). HYAL3 also exhibited an acceptable diagnostic ability for the pathological stage of BLCA (area under the receiver-operating characteristic curve = 0.769). Furthermore, HYAL3 acted as an independent prognostic factor in BLCA patients and correlated with the infiltration of various types of immunocytes, including B cells, CD8 T cells, cytotoxic cells, T follicular helper cells, and T helper (Th) 2 cells.
HYAL3 might serve as a potential biomarker for predicting poor OS in BLCA patients and correlated with immunocyte infiltration in BLCA.
已有研究表明,透明质酸(HA)可能调节膀胱癌(BLCA)的发生和发展。HYAL3 编码透明质酸酶,是 BLCA 的潜在治疗靶点。本研究旨在探讨 HYAL3 在 BLCA 发病机制中的作用。
利用癌症基因组图谱(TCGA)数据库和基因表达综合数据库(GEO)队列分析 BLCA 标本中 HYAL3 的表达,并在细胞系和人类蛋白质图谱中进行验证。然后,通过生存曲线和受试者工作特征(ROC)曲线分析 HYAL3 表达与临床病理数据之间的关系。通过京都基因与基因组百科全书(KEGG)通路分析和蛋白质-蛋白质相互作用网络进一步剖析 HYAL3 的功能。最后,我们利用肿瘤免疫估计资源和基因表达谱交互分析,获得 HYAL3 表达、浸润免疫细胞与相应免疫标志物集之间的相关性。
HYAL3 在多种癌症之间的表达差异很大。此外,在 TCGA-BLCA 和 GEO 基因芯片中,较高的 HYAL3 表达水平预示着总体生存率(OS)较差(P<0.05)。HYAL3 对 BLCA 的病理分期也具有较好的诊断能力(ROC 曲线下面积=0.769)。此外,HYAL3 是 BLCA 患者的独立预后因素,与各种类型免疫细胞的浸润相关,包括 B 细胞、CD8 T 细胞、细胞毒性细胞、滤泡辅助 T 细胞和 Th2 细胞。
HYAL3 可能是预测 BLCA 患者 OS 不良的潜在生物标志物,与 BLCA 中免疫细胞浸润相关。