Kim Seon Hyun, Kim Hye Jung, Kim Yeong Joo, Kim Yun Hak, Park Hae Ryoun
Periodontal Disease Signaling Network Research Center (MRC), School of Dentistry, Pusan National University, Yangsan, Korea.
Interdisciplinary Program of Genomic Data Science, Pusan National University, Yangsan, Korea.
Oral Dis. 2024 Nov;30(8):4909-4920. doi: 10.1111/odi.14987. Epub 2024 May 30.
This study aimed to screen oral squamous cell carcinoma (OSCC) diagnostic and prognostic candidates and investigate the potential functions and mechanisms of candidates in the chemoresistance of OSCC cell lines.
Differential expression profiling of lncRNA was performed in a large cohort of OSCC patients from the Cancer Genome Atlas database to identify OSCC diagnostic and prognostic candidates. Taxol resistance in OSCC cell lines was analyzed using MTT assay. OSCC cell lines transfected with EIF3J-DT pcDNA or siRNA were used to determine its regulatory effects on apoptosis, cell cycle distribution and autophagy using flow cytometry and western blot.
We identified EIF3J-DT as a candidate for OSCC diagnosis and prognosis. The expression level of EIF3J-DT in OSCC cell lines correlates with taxol resistance. EIF3J-DT silencing attenuated taxol resistance, and EIF3J-DT overexpression enhanced taxol resistance in OSCC cell lines. Silencing of EIF3J-DT reduced taxol resistance by inducing apoptosis, cell cycle arrest, and ATG14-mediated autophagy inhibition in OSCC cell lines.
We found that EIF3J-DT induced chemoresistance by regulating apoptosis, cell cycle, and autophagy in OSCC cell lines, which EIF3J-DT might provide a novel therapeutic approach for OSCC as well as a diagnostic and prognostic factor.
本研究旨在筛选口腔鳞状细胞癌(OSCC)的诊断和预后候选指标,并研究这些候选指标在OSCC细胞系化疗耐药中的潜在功能及机制。
利用癌症基因组图谱数据库中大量OSCC患者队列进行lncRNA差异表达谱分析,以鉴定OSCC诊断和预后候选指标。采用MTT法分析OSCC细胞系对紫杉醇的耐药性。用EIF3J-DT pcDNA或siRNA转染OSCC细胞系,通过流式细胞术和蛋白质免疫印迹法测定其对细胞凋亡、细胞周期分布和自噬的调控作用。
我们鉴定出EIF3J-DT作为OSCC诊断和预后的候选指标。EIF3J-DT在OSCC细胞系中的表达水平与紫杉醇耐药相关。EIF3J-DT基因沉默减弱了OSCC细胞系对紫杉醇的耐药性,而EIF3J-DT过表达增强了其耐药性。EIF3J-DT基因沉默通过诱导OSCC细胞系凋亡、细胞周期阻滞和ATG14介导的自噬抑制来降低紫杉醇耐药性。
我们发现EIF3J-DT通过调节OSCC细胞系的凋亡、细胞周期和自噬诱导化疗耐药,EIF3J-DT可能为OSCC提供一种新的治疗方法以及诊断和预后因子。