Wang Mengya, Jing Jingjing, Li Hao, Liu Jingwei, Yuan Yuan, Sun Liping
Tumor Etiology and Screening Department of Cancer Institute, and Key Laboratory of Cancer Etiology and Prevention in Liaoning Education Department, the First Hospital of China Medical University, Shenyang, China.
Key Laboratory of GI Cancer Etiology and Prevention in Liaoning Province, the First Hospital of China Medical University, Shenyang, China.
PeerJ. 2021 Feb 3;9:e10814. doi: 10.7717/peerj.10814. eCollection 2021.
Autophagy is an evolutionally highly conserved process, accompanied by the dynamic changes of various molecules, which is necessary for the orderly degradation and recycling of cellular components. The aim of the study was to identify the role of autophagy-related () genes in the occurrence and development of gastric cancer (GC).
Data from Oncomine dataset was used for the differential expression analysis between cancer and normal tissues. The association of genes expression with clinicopathologic indicators was evaluated by The Cancer Genome Atlas (TCGA) database and Gene Expression Omnibus (GEO) database. Moreover, using the TCGA datasets, the prognostic role of genes was assessed. A nomogram was further built to assess the independent prognostic factors.
The expression of autophagy-related genes , , , , , , , , and showed differences between cancer and normal tissues. After verification, and were significantly associated with TNM stage. , , and were associated with T stage. and were low-expressed in patients without lymph node metastasis. No gene in autophagy pathway was associated with M stage. Further multivariate analysis suggested that and were independent prognostic factors for GC. The C-index of nomogram was 0.676 and the 95% CI was 0.628 to 0.724.
Our study provided a comprehensive illustration of genes expression characteristics in GC. Abnormal expressions of the ubiquitin-like conjugated system in genes plays a key role in the occurrence of GC. sub-system may play an important role in development and clinical outcome of GC. In the future, it is necessary to further elucidate the alterations of specific forms in order to provide insights for the discovery, diagnosis, or targeting for GC.
自噬是一个进化上高度保守的过程,伴随着各种分子的动态变化,是细胞成分有序降解和循环所必需的。本研究的目的是确定自噬相关()基因在胃癌(GC)发生发展中的作用。
使用来自Oncomine数据集的数据进行癌组织与正常组织之间的差异表达分析。通过癌症基因组图谱(TCGA)数据库和基因表达综合数据库(GEO)评估基因表达与临床病理指标的相关性。此外,利用TCGA数据集评估基因的预后作用。进一步构建列线图以评估独立预后因素。
自噬相关基因、、、、、、、、和的表达在癌组织与正常组织之间存在差异。经验证,和与TNM分期显著相关。、和与T分期相关。和在无淋巴结转移的患者中低表达。自噬途径中没有基因与M分期相关。进一步的多变量分析表明,和是GC的独立预后因素。列线图的C指数为0.676,95%置信区间为0.628至0.724。
我们的研究全面阐述了基因在GC中的表达特征。基因中泛素样缀合系统的异常表达在GC的发生中起关键作用。子系统可能在GC的发展和临床结局中起重要作用。未来,有必要进一步阐明特定形式的改变,以便为GC的发现、诊断或靶向治疗提供见解。