PFDN6 contributes to colorectal cancer progression via transcriptional regulation

Fenghua Xu, Lingyang Kong, Xiao Sun, WenXiang Hui, Lan Jiang, Wenxin Han, ZhiFeng Xiao, Ning Li, DongFeng Chen, Nan Zheng, Jing Han, Lei Liu
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Abstract

Colorectal cancer (CRC) is a common cancer worldwide. Although there are several treatments for cancer, the therapeutic effect on CRC remains unsatisfactory, and it is imperative to identify new therapeutic targets.Prefoldin (PFDN) is mainly used in the cytoskeleton assembly during the folding of actin and tubulin monomers. However, whether PFDN subunits are involved in regulating the development of CRC remains to be elucidated. In this study, molecular biology, cell culture, transcriptome sequencing and other experimental techniques, combined with bioinformatics, were used to verify the regulatory effects of PFDN6 on CRC.PFDN6 expression is elevated in patients with CRC and is closely associated with the development of CRC. Knockdown of PFDN6 reduced the tumour cell number, promoted apoptosis, and inhibited the migration and invasion of CRC cells in HCT-116 and RKO cell lines. Mechanistically, differentially expressed genes and related signalling pathways in RKO cells after PFDN6 knockdown were analysed by transcriptome sequencing.PFDN6 was found to regulate the generation and development of CRC by targeting ZNF575. These results open new avenues for therapeutic interventions for patients with CRC.
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PFDN6 通过转录调控促进结直肠癌进展
结直肠癌(CRC)是全球常见的癌症。尽管目前有多种治疗癌症的方法,但对 CRC 的治疗效果仍不理想,因此寻找新的治疗靶点势在必行。预折叠蛋白(PFDN)主要用于细胞骨架组装过程中肌动蛋白和微管蛋白单体的折叠。然而,PFDN亚基是否参与调控CRC的发展仍有待阐明。本研究采用分子生物学、细胞培养、转录组测序等实验技术,并结合生物信息学,验证了PFDN6对CRC的调控作用。在HCT-116和RKO细胞系中,敲除PFDN6可减少肿瘤细胞数量,促进细胞凋亡,抑制CRC细胞的迁移和侵袭。通过转录组测序分析了PFDN6敲除后RKO细胞中不同表达基因及相关信号通路的机制。这些结果为CRC患者的治疗干预开辟了新途径。
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