Ma Sai, Sa Longqi, Zhang Jitao, Jiang Kuo, Mi Baoguo, Shan Lequn
Air Force Medical University, School of Stomatology, National Clinical Research Centre for Oral Disease, State Key Laboratory of Military Stomatology, Department of Prosthodontics, Shaanxi Key Laboratory of Stomatology, Xi'an, Shaanxi, China.
Xi'an Jiaotong University, Honghui Hospital, Department of Spine Surgery, Xi'an, Shaanxi, China.
Genet Mol Biol. 2023 Sep 25;46(3):e20230002. doi: 10.1590/1678-4685-GMB-2023-0002. eCollection 2023.
KDELR2 has been reported as a promotive factor for the genesis and progression of several malignancies. However, it is uncertain how it affects bladder urothelial carcinoma (BLCA). Using data extracted from online databases, an enhanced expression of KDELR2 in BLCA tissues was verified. Overexpression of KDELR2 was correlated with advanced clinicopathologic characteristics and unfavourable prognosis of BLCA. Receiver operating characteristic analysis highlighted the potential diagnostic value of KDELR2. Univariate and multivariate logistic regression analyses further revealed the predictive effect of KDELR2 for the prognosis of BLCA. KDELR2 was primarily enriched in biological functions related to organization of the extracellular matrix. TIMER, ssGSEA and GEPIA analyses suggested that KDELR2 expression is positively related to the infiltration of macrophages, Th2 cells and neutrophils. Finally, knocking-down of KDELR2 in T24 cells resulted in reduced proliferation, migration and macrophages recruitment. These results suggest that KDELR2 overexpression is an indicator for poor prognosis of BLCA and it has the potential to be employed as an immunotherapy target for BLCA.
KDELR2已被报道为几种恶性肿瘤发生和进展的促进因子。然而,其如何影响膀胱尿路上皮癌(BLCA)尚不确定。利用从在线数据库提取的数据,证实了KDELR2在BLCA组织中的表达增强。KDELR2的过表达与BLCA的晚期临床病理特征及不良预后相关。受试者工作特征分析突出了KDELR2的潜在诊断价值。单因素和多因素逻辑回归分析进一步揭示了KDELR2对BLCA预后的预测作用。KDELR2主要富集于与细胞外基质组织相关的生物学功能中。TIMER、单样本基因集富集分析(ssGSEA)和基因表达谱交互分析(GEPIA)表明,KDELR2表达与巨噬细胞、Th2细胞和中性粒细胞的浸润呈正相关。最后,敲低T24细胞中的KDELR2导致细胞增殖、迁移及巨噬细胞募集减少。这些结果表明,KDELR2过表达是BLCA预后不良的一个指标,并且它有潜力被用作BLCA的免疫治疗靶点。