Ask about this productRelated genes to: LONRF3 Blocking Peptide
- Gene:
- LONRF3 NIH gene
- Name:
- LON peptidase N-terminal domain and ring finger 3
- Previous symbol:
- RNF127
- Synonyms:
- FLJ22612
- Chromosome:
- Xq24
- Locus Type:
- gene with protein product
- Date approved:
- 2003-05-21
- Date modifiied:
- 2014-11-19
Related products to: LONRF3 Blocking Peptide
Related articles to: LONRF3 Blocking Peptide
- Idiopathic pulmonary fibrosis (IPF) is a deadly lung disease and currently has limited treatment options. E3 ubiquitin ligases play a role in multiple diseases; however, there are few studies involving them in the development of IPF. This study aimed to develop an E3 ubiquitin ligase gene-based risk signature model to predict the prognosis of patients with IPF. - Source: PubMed
Liu JunhuiZhu LongfeiLi GuirongChen Jingyu - M2-like tumor-associated macrophages (M2-like TAMs) function crucially in the tumor microenvironment (TME) and cancer development. This study developed a prognostic signature based on M2-like TAM-related genes for breast cancer (BRCA) applying transcriptome and scRNA-seq analysis. - Source: PubMed
Publication date: 2025/03/25
Xu YanghaochenLin PeiyanZhu YeZhang QingZhou Jinhong - Pancreatic cancer is one of the major malignancies and causes of mortality worldwide. E3 ubiquitin-protein ligases transfer activated ubiquitin from ubiquitin-conjugating enzymes to protein substrates and confer substrate specificity in cancer. In this study, we first downloaded data from The Cancer Genome Atlas pancreatic adenocarcinoma dataset, acquired all 27 differentially expressed genes (DEGs), and identified genomic alterations. Then, the prognostic significance of DEGs was analyzed, and eight DEGs (MECOM, CBLC, MARCHF4, RNF166, TRIM46, LONRF3, RNF39, and RNF223) and two clinical parameters (pathological N stage and T stage) exhibited prognostic significance. RNF223 showed independent significance as an unfavorable prognostic marker and was chosen for subsequent analysis. Next, the function of RNF223 in the pancreatic cancer cell lines ASPC-1 and PANC-1 was investigated, and RNF223 silencing promoted pancreatic cancer growth and migration. To explore the potential targets and pathways of RNF223 in pancreatic cancer, quantitative proteomics was applied to analyze differentially expressed proteins, and metabolism-related pathways were primarily enriched. Finally, the reason for the elevated expression of RNF223 was analyzed, and KLF4 was shown to contribute to the increased expression of RNF233. In conclusion, this study comprehensively analyzed the clinical significance of E3 ligases. Functional assays revealed that RNF223 promotes cancer by regulating cell metabolism. Finally, the elevated expression of RNF223 was attributed to KLF4-mediated transcriptional activation. This study broadens our knowledge regarding E3 ubiquitin ligases and signal transduction and provides novel markers and therapeutic targets in pancreatic cancer. - Source: PubMed
Publication date: 2021/10/14
Feng LeiWang JieqingZhang JianminDiao JingfangHe LongguangFu ChaoyiLiao HuiXu XiaopingGao YiZhou Chenjie