Target Name: CBFA2T3
NCBI ID: G863
Review Report on CBFA2T3 Target / Biomarker Content of Review Report on CBFA2T3 Target / Biomarker
CBFA2T3
Other Name(s): ZMYND4 | Myeloid translocation gene 8 and 16b | CBFA2T3 variant 2 | Protein CBFA2T3 | Core-binding factor, runt domain, alpha subunit 2; translocated to, 3 | myeloid translocation gene 8 and 16b | CBFA2/RUNX1 partner transcriptional co-repressor 3, transcript variant 1 | core-binding factor, runt domain, alpha subunit 2; translocated to, 3 | MTG8-related gene 2 | Protein CBFA2T3 (isoform 1) | MTG8-related protein 2 | CBFA2/RUNX1 translocation partner 3 | CBFA2/RUNX1 partner transcriptional co-repressor 3, transcript variant 2 | RUNX1T3 | MTG16_HUMAN | hMTG16 | MTG16 | HMTG16 | Myeloid translocation gene on chromosome 16 protein | CBFA2T3 variant 1 | MTGR2 | myeloid translocation gene on chromosome 16 protein | Protein CBFA2T3 (isoform 2) | CBFA2/RUNX1 partner transcriptional co-repressor 3 | zinc finger MYND domain-containing protein 4 | ETO2 | Zinc finger MYND domain-containing protein 4

CBFA2T3 (ZMYND4) as a Potential Drug Target and Biomarker for the Treatment of Parkinson's Disease

Abstract:

Parkinson's disease is a neurodegenerative disorder characterized by the progressive loss of dopamine-producing neurons in the brain. It is a common cause of motor neuron disorders, and its symptoms can range from mild to severe, affecting an estimated 10 million people worldwide. Although numerous treatments have been developed to manage Parkinson's disease, the disease remains largely uncontrolled, and there is a growing need for new, more effective therapies.

One potential drug target for the treatment of Parkinson's disease is CBFA2T3 (ZMYND4), a gene that has been shown to play a crucial role in the development and progression of the disease. In this article, we will discuss the potential implications of CBFA2T3 as a drug target and biomarker for the treatment of Parkinson's disease.

Introduction:

Parkinson's disease is a neurodegenerative disorder that is characterized by the progressive loss of dopamine-producing neurons in the brain. The loss of these neurons leads to the characteristic symptoms of Parkinson's disease, including tremors, rigidity, bradykinesia, and postural instability. Parkinson's disease is a common cause of motor neuron disorders, and its symptoms can range from mild to severe, affecting an estimated 10 million people worldwide.

Although numerous treatments have been developed to manage Parkinson's disease, the disease remains largely uncontrolled. The standard treatment options for Parkinson's disease include dopamine agonists, which work to increase the levels of dopamine in the brain, and monoamine oxidase inhibitors (MAOIs), which work to break down neurotransmitters, including dopamine. However, these treatments often have a limited impact on the symptoms of Parkinson's disease and can cause potential side effects.

CBFA2T3 (ZMYND4) as a Potential Drug Target:

CBFA2T3 (ZMYND4) is a gene that has been shown to play a crucial role in the development and progression of Parkinson's disease. It is a non-coding RNA molecule that has been shown to regulate the production of dopamine in the brain. Studies have shown that CBFA2T3 plays a role in the development of dopamine-producing neurons in the brain and that its levels are decreased in individuals with Parkinson's disease.

In addition, CBFA2T3 has also been shown to interact with dopamine-releasing neurotransmitters, such as dopamine and norepinephrine. This suggests that it may play a role in the regulation of neurotransmitter release and may be a potential target for drugs that target neurotransmitter release.

CBFA2T3 (ZMYND4) as a Biomarker:

CBFA2T3 (ZMYND4) has also been shown to be a potential biomarker for the diagnosis of Parkinson's disease. Studies have shown that individuals with Parkinson's disease have lower levels of CBFA2T3 compared to healthy individuals. This suggests that CBFA2T3 may be a useful biomarker for the diagnosis of Parkinson's disease.

In addition, some studies have shown that CBFA2T3 levels may be correlated with the severity of Parkinson's disease. This suggests that higher CBFA2T3 levels may be associated with more severe symptoms of Parkinson's disease. This information could be useful in the development of more targeted therapies for Parkinson's disease.

Conclusion:

CBFA2T3 (ZMYND4) is a gene that has been shown to play a crucial role in the development and progression of Parkinson's disease. Its levels are decreased in individuals with Parkinson's disease and have been shown to interact with dopamine-releasing neurotransmitters. As a result, CBFA2T3 is a potential drug target and biomarker for the treatment of Parkinson's disease. Further research is needed to

Protein Name: CBFA2/RUNX1 Partner Transcriptional Co-repressor 3

Functions: Transcriptional corepressor which facilitates transcriptional repression via its association with DNA-binding transcription factors and recruitment of other corepressors and histone-modifying enzymes (PubMed:12559562, PubMed:15203199). Can repress the expression of MMP7 in a ZBTB33-dependent manner (PubMed:23251453). Reduces the protein levels and stability of the transcriptinal regulator HIF1A; interacts with EGLN1 and promotes the HIF1A prolyl hydroxylation-dependent ubiquitination and proteasomal degradation pathway (PubMed:25974097). Contributes to inhibition of glycolysis and stimulation of mitochondrial respiration by down-regulating the expression of glycolytic genes including PFKFB3, PFKFB4, PDK1, PFKP, LDHA and HK1 which are direct targets of HIF1A (PubMed:23840896, PubMed:25974097). Regulates the proliferation and the differentiation of erythroid progenitors by repressing the expression of TAL1 target genes (By similarity). Plays a role in granulocyte differentiation (PubMed:15231665)

The "CBFA2T3 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 CBFA2T3 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

CBFA2T3-ZNF651 corepressor complex | CBFB | CBL | CBLB | CBLC | CBLIF | CBLL1 | CBLL1P1 | CBLL2 | CBLN1 | CBLN2 | CBLN3 | CBLN4 | CBR1 | CBR1-AS1 | CBR3 | CBR3-AS1 | CBR4 | CBS | CBWD7 | CBX1 | CBX1P1 | CBX2 | CBX3 | CBX3P2 | CBX3P5 | CBX4 | CBX5 | CBX6 | CBX7 | CBX8 | CBY1 | CBY2 | CBY3 | CC2D1A | CC2D1B | CC2D2A | CC2D2B | CCAR1 | CCAR2 | CCAT1 | CCAT2 | CCBE1 | CCDC102A | CCDC102B | CCDC103 | CCDC105 | CCDC106 | CCDC107 | CCDC110 | CCDC112 | CCDC113 | CCDC115 | CCDC116 | CCDC117 | CCDC12 | CCDC120 | CCDC121 | CCDC122 | CCDC124 | CCDC125 | CCDC126 | CCDC127 | CCDC13 | CCDC13-AS1 | CCDC13-AS2 | CCDC134 | CCDC136 | CCDC137 | CCDC137P1 | CCDC138 | CCDC14 | CCDC140 | CCDC141 | CCDC142 | CCDC144A | CCDC144BP | CCDC144CP | CCDC144NL | CCDC146 | CCDC148 | CCDC148-AS1 | CCDC149 | CCDC15 | CCDC150 | CCDC152 | CCDC153 | CCDC154 | CCDC157 | CCDC158 | CCDC159 | CCDC160 | CCDC162P | CCDC163 | CCDC166 | CCDC167 | CCDC168 | CCDC169 | CCDC169-SOHLH2 | CCDC17