School of Dentistry, Chung Shan Medical University, Taichung, Taiwan; Department of Dentistry, Chung Shan Medical University Hospital, Taichung, Taiwan.
School of Dentistry, Chung Shan Medical University, Taichung, Taiwan; Department of Dentistry, Chung Shan Medical University Hospital, Taichung, Taiwan; Institute of Oral Sciences, Chung Shan Medical University, Taichung, Taiwan.
J Formos Med Assoc. 2020 Oct;119(10):1532-1538. doi: 10.1016/j.jfma.2020.06.004. Epub 2020 Jun 14.
BACKGROUND/PURPOSE: Oral cancer is amongst the most prevalent cancers worldwide with rising incidence. Various attempts have been made to elucidate its pathogenesis, and we sought to examine the function of a ubiquitin E3 ligase that was encoded by STUB1.
The mRNA expression of STUB1 in oral cancer samples and normal counterparts was determined by qRT-PCR. Numerous assays to assess the features of cancer cells, including self-renewal capacity, invasion and migration abilities were conducted following knockdown or overexpression of STUB1.
The expression level of STUB1 was reduced in oral cancer, which was associated with a reduced relapse-free survival. Two oral cancer cell lines with low expression of STUB1 (SAS and HSC3) were chosen for the overexpression of STUB1. We showed that ectopic expression of STUB1 led to the downregulation of TGM2, a multifunctional protein that contributed to cancer progression in several cancers. Our results demonstrated that overexpression of STUB1 suppressed the cancer aggressiveness, while restoration of TGM2 reverted the effects. Last, we showed that STUB1 silencing resulted in enhanced cancer features.
The abnormal downregulation of STUB1 may lessen its suppressive effect on TGM2, which induced the onset or exacerbated the progression of oral cancer. The therapeutic approach to enhance the expression of STUB1 could be a promising direction for cancer therapy.
背景/目的:口腔癌是全球最常见的癌症之一,其发病率呈上升趋势。人们已经尝试了多种方法来阐明其发病机制,我们试图研究一种由 STUB1 编码的泛素 E3 连接酶的功能。
通过 qRT-PCR 确定口腔癌样本和正常对照中 STUB1 的 mRNA 表达。在敲低或过表达 STUB1 后,进行了多种评估癌细胞特征的实验,包括自我更新能力、侵袭和迁移能力。
STUB1 的表达水平在口腔癌中降低,与无复发生存率降低有关。我们选择了两个 STUB1 低表达的口腔癌细胞系(SAS 和 HSC3)用于过表达 STUB1。我们表明,STUB1 的异位表达导致多功能蛋白 TGM2 的下调,TGM2 在多种癌症中促进癌症进展。我们的结果表明,过表达 STUB1 抑制了癌症的侵袭性,而恢复 TGM2 则逆转了这种作用。最后,我们表明 STUB1 的沉默导致了癌症特征的增强。
STUB1 的异常下调可能会降低其对 TGM2 的抑制作用,从而引发或加剧口腔癌的发生或进展。增强 STUB1 表达的治疗方法可能是癌症治疗的一个有前途的方向。