在人类疾病中,CRNDE是一个潜在的治疗目标
Shiyun Zeng1,2, Yao Xie1,3, Yulan Shi1,3
1Third-grade Pharmacological Laboratory on Traditional Chinese Medicine, State Administration of Traditional Chinese Medicine, China Three Gorges University, Yichang, 443002, China.
Current pharmaceutical design
|March 28, 2025
概括
大肠直肠瘤差异表达 (CRNDE) 是一种长非编码RNA (lncRNA),涉及癌症和非癌症疾病. 它的调制影响患者的生存,有助于疾病诊断,突出其治疗潜力.
科学领域:
- 分子生物学分子生物学
- 基因组学就是基因组学.
- 在瘤学瘤学.
背景情况:
- 长非编码RNA (lncRNAs) 在生物过程中起着至关重要的作用,挑战了对非编码RNA功能的传统观点.
- 差异表达结肠直肠瘤 (CRNDE) 是一种致癌性 lncRNA,在各种疾病中具有重大影响.
研究的目的:
- 审查CRNDE在人类疾病中的表达模式,包括癌症和非癌症疾病.
- 阐明CRNDE在疾病进展中的作用和潜在的分子机制.
- 探索针对CRNDE的最新治疗策略.
主要方法:
- 对研究在人类疾病中研究CRNDE表达和功能的文献综述.
- 分析CRNDE对疾病进展和患者结果的影响.
- 检查CRNDE的诊断和治疗潜力.
主要成果:
- 在各种癌症中,CRNDE表达是不受调节的,调节显著改善了患者的生存率 (例如,从19.2到32.5个月).
- CRNDE还在COVID-19等非恶性疾病中显示出改变的表达,在那里它作为具有高精度 (0.889) 的诊断指标.
结论:
- CRNDE是一种多功能分子,在瘤发生和非癌症病理学中发挥着重要作用.
- 作为诊断的潜在生物标志物和各种人类疾病的治疗目标,CRNDE具有前景.
相关概念视频
CRISPR
Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced Short...
G Protein-coupled Receptors
G Protein-Coupled Receptors or GPCRs are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to sensory stimuli such as light, odors, hormones, cytokines, or neurotransmitters.
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
Drug Discovery: Overview
Drug discovery is a multifaceted process involving extensive screening, testing, and optimization of lead compounds to identify potential new drugs for therapeutic use. It combines several approaches, including screening large numbers of natural products, chemical modification of known active molecules, identification of new drug targets, and rational design based on biological mechanisms and drug-receptor structure. These approaches are carried out in both academic research laboratories and...
Targets for Drug Action: Overview
Drugs target macromolecules to modify ongoing cellular processes. Primary drug targets include receptors, ion channels, transporters, and enzymes.
Receptors are either membrane-spanning or intracellular proteins, which upon binding a ligand, get activated and transmit the signal downstream to elicit a response. Drugs bind receptors, either mimicking the action of endogenous ligands or blocking the receptor activity to bring about a modified response. Nearly 35% of approved drugs target the G...
Receptors are either membrane-spanning or intracellular proteins, which upon binding a ligand, get activated and transmit the signal downstream to elicit a response. Drugs bind receptors, either mimicking the action of endogenous ligands or blocking the receptor activity to bring about a modified response. Nearly 35% of approved drugs target the G...
Transducer Mechanism: Enzyme-Linked Receptors
Enzyme-linked receptors are cell-surface receptors acting as an enzyme or associating with an enzyme intracellularly. They make excellent drug targets. Drugs can bind to the extracellular ligand-binding domain or directly affect their enzymatic domain and alter their activity.
Major types that are helpful drug targets include:
Major types that are helpful drug targets include:
Pharmacogenomics: Identification of New Drug Targets
Advances in genomics have profoundly influenced drug discovery by increasing both the speed and accuracy of pharmaceutical development. Pharmacogenomics, which examines how genetic variation influences drug response, facilitates the identification of novel therapeutic targets and enables patient stratification for personalized treatment. These strategies contribute to improved drug efficacy, minimized adverse effects, and more efficient clinical trial design.Mapping genetic differences...


