Target Name: RPL23AP25
NCBI ID: G653789
Review Report on RPL23AP25 Target / Biomarker Content of Review Report on RPL23AP25 Target / Biomarker
RPL23AP25
Other Name(s): RPL23A_7_192 | Ribosomal protein L23a pseudogene 25 | ribosomal protein L23a pseudogene 25

RPL23AP25: A Potential Drug Target and Biomarker for ALZHEIMER'S DISEASE

Alzheimer's disease is a progressive neurological disorder that affects millions of people worldwide, leading to a significant impact on society. It is characterized by the accumulation of neurofibrillary tangles and beta-amyloid plaques in the brain, which cause damage to nerve cells and lead to cognitive decline. Currently, there is no cure for Alzheimer's disease, and the only available treatment is supportive care, which aims to alleviate symptoms and improve quality of life. Therefore, identifying potential drug targets and biomarkers for Alzheimer's disease remains a major focus in research.

RPL23A_7_192: A Potential Drug Target

The RNA-protein homeostasis regulator (RPL23A) is a gene that has been well-studied in various organisms, including humans. It is a key regulator of mitochondrial dynamics, and its dysfunction has been implicated in various diseases, including Alzheimer's disease. RPL23A_7_192 is a specific isoform of RPL23A that has been shown to promote the import of aggregated beta-amyloid peptides into the mitochondria. This process is critical for the formation of beta-amyloid plaques, which are a hallmark of Alzheimer's disease.

Recent studies have suggested that RPL23A_7_192 may be a potential drug target for Alzheimer's disease. By inhibiting the import of beta-amyloid peptides into the mitochondria, researchers may be able to reduce the formation of beta-amyloid plaques and slow down the progression of Alzheimer's disease. In addition, RPL23A_7_192 has been shown to be involved in the regulation of cellular processes that are important for the survival of nerve cells. Therefore, targeting RPL23A_7_192 with drugs that can modulate its activity may be a promising strategy for the development of new treatments for Alzheimer's disease.

Biomarker Potential

The diagnostic diagnosis of Alzheimer's disease is based on the presence of beta-amyloid plaques and neurofibrillary tangles in the brain. However, these changes can occur years before the onset of symptoms, making it difficult to diagnose the disease at an early stage. Therefore, the development of biomarkers that can predict the risk of Alzheimer's disease and slow down the progression of the disease is crucial.

RPL23A_7_192 has been shown to be involved in the regulation of various cellular processes that are important for the survival of nerve cells. Its expression has been associated with the survival of dopamine-producing neurons in the brain. Therefore, RPL23A_7_192 may be a useful biomarker for the diagnosis and prognosis of Alzheimer's disease.

In addition, RPL23A_7_192 has been shown to be involved in the regulation of mitochondrial dynamics. Its expression has been associated with the import of beta-amyloid peptides into the mitochondria, which is critical for the formation of beta-amyloid plaques. Therefore, the expression of RPL23A_7_192 may be a useful biomarker for the assessment of the severity of beta-amyloid plaque formation in individuals at risk for Alzheimer's disease.

Conclusion

In conclusion, RPL23A_7_192 is a potential drug target for Alzheimer's disease. Its expression has been shown to be involved in the regulation of various cellular processes that are important for the survival of nerve cells and the formation of beta-amyloid plaques. Therefore, targeting RPL23A_7_192 with drugs that can modulate its activity may be a promising strategy for the development of new treatments for Alzheimer's disease. Further research is needed to confirm its potential as a drug target and to develop biomarkers that can predict the risk and progression of Alzheimer's disease.

Protein Name: Ribosomal Protein L23a Pseudogene 25

The "RPL23AP25 Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about RPL23AP25 comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

More Common Targets

RPL23AP3 | RPL23AP32 | RPL23AP34 | RPL23AP42 | RPL23AP43 | RPL23AP44 | RPL23AP45 | RPL23AP5 | RPL23AP53 | RPL23AP56 | RPL23AP57 | RPL23AP6 | RPL23AP61 | RPL23AP63 | RPL23AP64 | RPL23AP7 | RPL23AP79 | RPL23AP82 | RPL23AP87 | RPL23P6 | RPL23P8 | RPL24 | RPL24P2 | RPL24P7 | RPL26 | RPL26L1 | RPL26L1-AS1 | RPL26P12 | RPL26P13 | RPL26P21 | RPL26P30 | RPL26P32 | RPL26P36 | RPL27 | RPL27A | RPL27AP6 | RPL27P11 | RPL28 | RPL28P1 | RPL29 | RPL29P11 | RPL29P12 | RPL29P14 | RPL29P19 | RPL29P2 | RPL29P20 | RPL29P30 | RPL29P4 | RPL29P5 | RPL29P6 | RPL3 | RPL30 | RPL30P6 | RPL31 | RPL31P10 | RPL31P11 | RPL31P13 | RPL31P18 | RPL31P23 | RPL31P32 | RPL31P37 | RPL31P39 | RPL31P4 | RPL31P43 | RPL31P51 | RPL31P63 | RPL32 | RPL32P17 | RPL32P18 | RPL32P19 | RPL32P22 | RPL32P29 | RPL32P3 | RPL32P7 | RPL34 | RPL34-DT | RPL34P14 | RPL34P34 | RPL35 | RPL35A | RPL35AP26 | RPL35AP30 | RPL35AP32 | RPL35AP33 | RPL35AP36 | RPL35P8 | RPL36 | RPL36A | RPL36A-HNRNPH2 | RPL36AL | RPL36AP15 | RPL36AP17 | RPL36AP33 | RPL36AP37 | RPL36AP44 | RPL36AP49 | RPL36AP8 | RPL36P13 | RPL36P14 | RPL36P5