Chang Ying-Hsu, Lin Po-Hung, Chen Chin-Chang, Weng Wen-Hui, Yu Kai-Jie, Liu Chung-Yi, Hsieh Chin-Hsuan, Chang Tzu-Hsuan, Shao I-Hung, Kan Hung-Cheng, Chuang Cheng-Keng, Pang See-Tong
Department of Urology, New Taipei Municipal Tucheng Hospital, Chang Gung Memorial Hospital, New Taipei City 236017, Taiwan, R.O.C.
Division of Urology, Department of Surgery, Chang Gung Memorial Hospital at Linkou, Taoyuan 33305, Taiwan, R.O.C.
Exp Ther Med. 2021 Nov;22(5):1204. doi: 10.3892/etm.2021.10638. Epub 2021 Aug 24.
The present study investigated the role of tubulin polymerization promoting protein (TPPP) in the regulation of bladder cancer (BC) cell proliferation and migration, in addition to the association between TPPP gene copy number amplification and clinicopathological characteristics of BC. TPPP gene amplification was measured in human BC epithelial cells and samples obtained from 52 patients with BC via fluorescence hybridization. TPPP gain was defined as mean TPPP copy number >2.2 per nucleus (cutoff). The neutrophil-to-lymphocyte ratio (NLR) was also obtained from the preoperative data of the patients. For assays, BC cell lines were transfected with either TPPP small interfering RNAs or scrambled control, following which cell proliferation and migration were determined using Cell Counting Kit-8 and Transwell migration assays, respectively. The percentage of cells with TPPP copy number amplification in the four BC epithelial cell lines (MGH-U1, -U1R, -U3, -U4) examined (86.0-100.0%) was found to be higher compared with that in the normal human uroepithelial cell lines (3.0 and 9.0%). Patients were divided into one- (1.9%), two- (55.8%), three- (7.7%), four- (26.9%) and five-copy (7.7%) types. Results calculated using Fisher's exact test indicated that the gain of TPPP in patients with BC associated significantly with age (P<0.05), advanced histological grade (P<0.001), tumor stage (P<0.05), histological type (P<0.001) and NLR (P<0.05). In MGH-U1R and MGH-U4 cells, cell proliferation and migration were revealed to be significantly lower following TPPP knockdown compared with those in cells transfected with the scrambled control. In conclusion, findings from the present study suggest that TPPP is important for cell proliferation, cell migration and BC progression, such that TPPP copy number assessment would be advised for preoperative urine cytology for urothelial neoplasia diagnosis.
本研究调查了微管蛋白聚合促进蛋白(TPPP)在膀胱癌(BC)细胞增殖和迁移调控中的作用,以及TPPP基因拷贝数扩增与BC临床病理特征之间的关联。通过荧光杂交法检测了人BC上皮细胞和52例BC患者样本中的TPPP基因扩增情况。TPPP增益定义为每个细胞核的平均TPPP拷贝数>2.2(临界值)。中性粒细胞与淋巴细胞比值(NLR)也取自患者的术前数据。在实验中,用TPPP小干扰RNA或乱序对照转染BC细胞系,随后分别使用细胞计数试剂盒-8和Transwell迁移实验测定细胞增殖和迁移情况。在所检测的四种BC上皮细胞系(MGH-U1、-U1R、-U3、-U4)中,TPPP拷贝数扩增细胞的百分比(86.0 - 100.0%)高于正常人尿路上皮细胞系(3.0%和9.0%)。患者分为一拷贝(1.9%)、两拷贝(55.8%)、三拷贝(7.7%)、四拷贝(26.9%)和五拷贝(7.7%)类型。使用Fisher精确检验计算的结果表明,BC患者中TPPP的增益与年龄(P<0.05)、高级组织学分级(P<0.001)、肿瘤分期(P<0.05)、组织学类型(P<0.001)和NLR(P<0.05)显著相关。在MGH-U1R和MGH-U4细胞中,与转染乱序对照的细胞相比,TPPP敲低后细胞增殖和迁移显著降低。总之,本研究结果表明,TPPP对细胞增殖、细胞迁移和BC进展很重要,因此建议在术前尿液细胞学检查中评估TPPP拷贝数,以诊断尿路上皮肿瘤。