College of Food Science and Nutritional Engineering, China Agricultural University, Beijing, China.
Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Biol Trace Elem Res. 2023 Sep;201(9):4349-4359. doi: 10.1007/s12011-022-03510-1. Epub 2022 Dec 6.
Exposure to cadmium (Cd), a non-essential heavy metal, leads to the malignant transformation of urothelial cells and promotes bladder cancer (BC) development, but the mechanisms are unclear. Therefore, we aimed to explore the possible molecules associated with Cd-related BC. By analyzing and mining biological big data in public databases, we screened genes associated with the malignant transformation of uroepithelial cells caused by Cd and further screened the key gene associated with BC prognosis from these genes. The possible roles of the key gene in BC progression were then further explored through biological big data analysis and cellular experiments. Data mining yielded a total of 387 malignant transformation-related genes, which were enriched in multiple cancer-related signaling pathways, such as cytokine-cytokine receptor interaction, Toll-like receptor signaling pathway, and Jak-STAT signaling pathway. Further screening identified Fibronectin 1 (FN1) as the key gene. High expression of FN1 was associated with the advanced pathologic stage, T stage, N stage, and M stage and predicted an unfavorable outcome in BC patients. FN1 expression was positively associated with the infiltration of several types of immune cells, particularly tumor-associated macrophages and cancer-associated fibroblasts. Overexpression of FN1 could be detected in Cd-treated urothelial cells and BC cell lines. Interestingly, silencing of FN1 impaired the proliferation and invasive capacity of BC cells. In conclusion, the present study provides new insight into the mechanism of Cd-related BC. FN1 might be a prognostic marker and therapeutic target for BC. Future studies are needed to confirm these results.
暴露于镉(Cd),一种非必需的重金属,导致尿路上皮细胞的恶性转化,并促进膀胱癌(BC)的发展,但机制尚不清楚。因此,我们旨在探索与 Cd 相关的 BC 相关的可能分子。通过分析和挖掘公共数据库中的生物大数据,我们筛选出与 Cd 引起的尿路上皮细胞恶性转化相关的基因,并进一步从这些基因中筛选出与 BC 预后相关的关键基因。然后通过生物大数据分析和细胞实验进一步探索关键基因在 BC 进展中的可能作用。数据挖掘共得到 387 个与恶性转化相关的基因,这些基因富集在多种癌症相关的信号通路中,如细胞因子-细胞因子受体相互作用、Toll 样受体信号通路和 Jak-STAT 信号通路。进一步筛选确定纤维连接蛋白 1(FN1)为关键基因。FN1 的高表达与 BC 患者的晚期病理分期、T 分期、N 分期和 M 分期相关,并预测预后不良。FN1 的表达与多种免疫细胞的浸润呈正相关,尤其是肿瘤相关巨噬细胞和癌症相关成纤维细胞。在 Cd 处理的尿路上皮细胞和 BC 细胞系中可以检测到 FN1 的过表达。有趣的是,FN1 的沉默会削弱 BC 细胞的增殖和侵袭能力。总之,本研究为 Cd 相关 BC 的机制提供了新的见解。FN1 可能是 BC 的预后标志物和治疗靶点。需要进一步的研究来证实这些结果。