Nur77 Serves as a Potential Prognostic Biomarker That Correlates with Immune Infiltration and May Act as a Good Target for Prostate adenocarcinoma.
Qiong-Ying HuJie LiuXiao-Kun ZhangWan-Ting YangYu-Tian TaoCe ChenYe-He QianJin-Shan TangXin-Sheng YaoYing-He XuJing-Hui WangPublished in: Molecules (Basel, Switzerland) (2023)
Prostate adenocarcinoma (PRAD) is the most frequent malignancy, and is the second leading cause of death due to cancer in men. Thus, new prognostic biomarkers and drug targets for PRAD are urgently needed. As we know, nuclear receptor Nur77 is important in cancer development and changes in the tumor microenvironment; whereas, the function of Nur77 in PRAD remains to be elucidated. The TCGA database was used to explore the Nur77 expression and its role in the prognosis of PRAD. It was shown that Nur77 was down regulated in PRAD, and low Nur77 expression was correlated with advanced clinical pathologic characteristics (high grade, histological type, age) and poor prognosis. Furthermore, key genes screening was examined by univariate Cox analysis and Kaplan-Meier survival. Additionally, Nur77 was closely related to immune infiltration and some anti-tumor immune functions. The differentially expressed genes (DEGs) were presented by protein-protein interaction (PPI) network analysis. Therefore, the expression level of Nur77 might help predict the survival of PRAD cases, which presents a new insight and a new target for the treatment of PRAD. In vitro experiments verified that natural product malayoside targeting Nur77 exhibited significant therapeutic effects on PRAD and largely induced cell apoptosis by up-regulating the expression of Nur77 and its mitochondrial localization. Taken together, Nur77 is a prognostic biomarker for patients with PRAD, which may refresh the profound understanding of PRAD individualized treatment.
Keyphrases
- poor prognosis
- long non coding rna
- high grade
- protein protein
- prostate cancer
- squamous cell carcinoma
- network analysis
- papillary thyroid
- binding protein
- genome wide
- emergency department
- locally advanced
- gene expression
- oxidative stress
- drug delivery
- dna methylation
- low grade
- high glucose
- adverse drug
- benign prostatic hyperplasia
- squamous cell
- human health