Department of Urology, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Department of Blood Transfusion, The First Affiliated Hospital of Nanchang University, Nanchang, China.
BMC Cancer. 2023 Aug 1;23(1):716. doi: 10.1186/s12885-023-11209-2.
TUBA1C is an α-tubulin isoform involved in mitosis, and its dysregulation has been implicated in tumor progression. There is still no clear understanding of its role in bladder urothelial carcinoma (BLCA).
This study examined the differential expression of TUBA1C and its prognostic significance in bladder cancer based on data from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) and also assessed the correlation of TUBA1C expression level with immune cell infiltration and immune checkpoint gene expression levels and the half-inhibitory concentration (IC50) of different chemotherapeutic agents. Immunotherapy response was estimated using the Tumor Immune Dysfunction and Exclusion (TIDE) algorithm. We detected TUBA1C expression in BLCA cells using PCR and Western blotting. Functional assays, including CCK-8, colony formation, transwell, apoptosis and cell cycle assays, were also performed to assess the oncogenic role of TUBA1C in BLCA.
In three independent public cohorts, TUBA1C was significantly upregulated in bladder tumor tissues, and high TUBA1C expression in bladder cancer was associated with a poorer outcome than low expression. TUBA1C was an independent prognostic risk factor for bladder cancer, and numerous immune checkpoint genes and infiltrating immune cells were associated with TUBA1C. TIDE analysis revealed that TUBA1C showed great potential for predicting the immunotherapy response in bladder cancer patients. In addition, drug sensitivity analysis revealed that high TUBA1C expression indicated sensitivity to multiple chemotherapeutic agents. Functional assays revealed that silencing TUBA1C significantly inhibited the proliferation, migration and invasion of BLCA cells and induced apoptosis and cell cycle arrest.
The overexpression of TUBA1C in bladder cancer predicts a poor prognosis and may also be a potential immunotherapeutic target. As a prognostic marker, TUBA1C influences tumor progression by regulating the cell cycle.
TUBA1C 是一种参与有丝分裂的α-微管蛋白同工型,其失调与肿瘤进展有关。目前,人们对其在膀胱尿路上皮癌(BLCA)中的作用仍缺乏清晰的认识。
本研究基于癌症基因组图谱(TCGA)和基因表达综合数据库(GEO)的数据,检测了 TUBA1C 在膀胱癌中的差异表达及其预后意义,并评估了 TUBA1C 表达水平与免疫细胞浸润和免疫检查点基因表达水平的相关性,以及不同化疗药物的半抑制浓度(IC50)。使用肿瘤免疫功能障碍和排斥(TIDE)算法评估免疫治疗反应。我们使用 PCR 和 Western blot 检测了 BLCA 细胞中的 TUBA1C 表达。还进行了 CCK-8、集落形成、Transwell、凋亡和细胞周期测定等功能测定,以评估 TUBA1C 在 BLCA 中的致癌作用。
在三个独立的公共队列中,TUBA1C 在膀胱肿瘤组织中显著上调,膀胱癌中 TUBA1C 高表达与低表达相比预后更差。TUBA1C 是膀胱癌的独立预后危险因素,许多免疫检查点基因和浸润免疫细胞与 TUBA1C 相关。TIDE 分析表明,TUBA1C 具有预测膀胱癌患者免疫治疗反应的巨大潜力。此外,药物敏感性分析表明,高 TUBA1C 表达提示对多种化疗药物敏感。功能测定表明,沉默 TUBA1C 可显著抑制 BLCA 细胞的增殖、迁移和侵袭,并诱导细胞凋亡和细胞周期停滞。
膀胱癌中 TUBA1C 的过表达预示着预后不良,也可能是一种潜在的免疫治疗靶点。作为一个预后标志物,TUBA1C 通过调节细胞周期影响肿瘤的进展。