Lu Ding-Jin, Wang Hai-Rong, Xu You-Sheng, Huang Hai-Bo, Zhong Qi-Gang, Luo Yuan-Ning, Qi Jian-Feng, Wu Hong-Chao, Pei Jin-Ye, Zhang Kun, Xu Chao-Xiong, Wang Tian-Xian, Zhang Wei, Zhou Yu-Hong, Huang Zhi-Guang, Wang Fu-Bo
Department of Urology, Beihai People's Hospital, Beihai 536000, Guangxi Zhuang Autonomous Region, China.
Department of Pathology, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China.
World J Clin Oncol. 2025 May 24;16(5):103830. doi: 10.5306/wjco.v16.i5.103830.
Bladder cancer (BLCA) is a common urological tumor. Homeobox C6 () is an HOX family gene that has an oncogenic effect in various malignancies.
To investigate the expression and function of in BLCA.
This study employed immunohistochemistry, along with global chip and sequencing data for BLCA, to comprehensively evaluate the protein and mRNA expression of in BLCA. RNA interference technology was employed to knock down the mRNA expression of in BLCA cells, and the impact of reduced expression on cellular function was assessed. Additionally, we explored the potential mechanisms of in BLCA by aggregating chromatin immunoprecipitation sequencing data.
The immunohistochemistry results, sequencing data, and microarray data revealed that both the mRNA and protein expressions of in BLCA were notably greater than the expressions in non-cancerous tissues. Knocking down the expression of considerably limited the function of cell proliferation, migration, and invasion abilities of BLCA cells, elevated cell apoptosis, and triggered the G0/G1 phase blockade. The potential target genes of were enriched in pathways such as chemical carcinogenesis and reactive oxygen species. A notable positive correlation between mRNA expression and its target gene timeless circadian regulator () was revealed. Notable binding peak signals for were identified in the promoter region of .
is upregulated in BLCA and may influence the cellular functions of BLCA by regulating the expression of the target gene .
膀胱癌(BLCA)是一种常见的泌尿系统肿瘤。同源盒C6()是一种HOX家族基因,在各种恶性肿瘤中具有致癌作用。
研究在BLCA中的表达及功能。
本研究采用免疫组织化学方法,并结合BLCA的全基因组芯片和测序数据,全面评估在BLCA中的蛋白质和mRNA表达。采用RNA干扰技术敲低BLCA细胞中的mRNA表达,并评估表达降低对细胞功能的影响。此外,我们通过整合染色质免疫沉淀测序数据,探索在BLCA中的潜在机制。
免疫组织化学结果、测序数据和微阵列数据显示,在BLCA中的mRNA和蛋白质表达均显著高于非癌组织中的表达。敲低的表达显著限制了BLCA细胞的增殖、迁移和侵袭能力,提高了细胞凋亡率,并引发了G0/G1期阻滞。的潜在靶基因富集于化学致癌和活性氧等通路。在mRNA表达与其靶基因 timeless昼夜节律调节因子()之间发现了显著的正相关。在的启动子区域鉴定到了显著的结合峰信号。
在BLCA中上调,可能通过调节靶基因的表达影响BLCA的细胞功能。