Target Name: CBY1
NCBI ID: G25776
Review Report on CBY1 Target / Biomarker Content of Review Report on CBY1 Target / Biomarker
CBY1
Other Name(s): coiled-coil protein PIGEA-14 | CBY | chibby family member 1, beta catenin antagonist | HS508I15A | chibby CTNNB1-mediated transcription inhibitor | CBY1 variant 2 | PIGEA-14 | Protein chibby homolog 1 | Chibby1 | Cytosolic leucine-rich protein | PIGEA14 | CBY1_HUMAN | Arb1 | PKD2 interactor, Golgi and endoplasmic reticulum-associated 1 | Polycystin-2 interactor, Golgi- and endoplasmic reticulum-associated protein, 14 kDa | Coiled-coil protein PIGEA-14 | ARPP-binding protein | Chibby family member 1, beta catenin antagonist, transcript variant 2 | arb1 | chibby homolog 1 | polycystin-2 interactor, Golgi- and endoplasmic reticulum-associated protein, 14 kDa | PGEA1 | PKD2 interactor, golgi and endoplasmic reticulum associated 1 | cytosolic leucine-rich protein | C22orf2

CBY1: A Potential Drug Target and Biomarker for Neurodegenerative Disorders

Neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, and Huntington's disease, are debilitating and life-threatening conditions that affect millions of people worldwide. These conditions are characterized by the progressive loss of brain cells, leading to a range of symptoms, including cognitive decline, tremors, and motor dysfunction. Despite advances in neuroimaging and disease staging, there is currently no cure for these disorders, and existing treatments are only able to manage symptoms and provide temporary relief. Therefore, the development of new drug targets and biomarkers has the potential to significantly improve treatment outcomes for neurodegenerative diseases.

CBY1: A Potential Drug Target and Biomarker

The protein CBY1, also known as coiled-coil protein PIGEA-14, has been identified as a potential drug target and biomarker for neurodegenerative disorders. CBY1 is a member of the PIGEA family of proteins, which are involved in various cellular processes, including cell signaling, cytoskeletal organization, and stress response. The PIGEA genes have been implicated in neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, and Huntington's disease.

CBY1 is expressed in a variety of tissues and cells, including brain, spinal cord, and peripheral tissues. It is involved in the regulation of cellular processes that are critical for maintaining neuronal structure and function. One of its key functions is to regulate the formation and maintenance of the microtubules that are responsible for transporting neurotransmitters and other cellular signaling molecules.

CBY1 has also been shown to play a role in the regulation of cellular stress responses. It is involved in the stress-induced translocation of the protein p21, which is a well-known stress-responsive protein that is involved in the regulation of cell cycle progression and apoptosis. The p21 protein is often activated in response to cellular stress, and its levels have been shown to be elevated in neurodegenerative diseases.

CBY1 is also involved in the regulation of cellular signaling pathways that are important for neuronal communication. It is a critical regulator of the neurotransmitter receptors, which are involved in the transmission of signals from the brain to other parts of the body. The neurotransmitter receptors are constantly being targeted by other proteins, including neurodegenerative diseases, and it is possible that CBY1 may play a role in the regulation of these receptor interactions.

CBY1 is also involved in the regulation of cellular processes that are critical for the maintenance of neuronal structural integrity. It is involved in the regulation of the formation and maintenance of the myelin sheath that surrounds the neuronal axons in the central nervous system. The myelin sheath is responsible for providing support and protection to the axons, and its loss is a hallmark feature of neurodegenerative diseases.

CBY1 has also been shown to play a role in the regulation of cellular processes that are important for the development and progression of neurodegenerative diseases. It is involved in the regulation of the production of reactive oxygen species (ROS), which are highly reactive molecules that can cause damage to cellular components and contribute to the development of neurodegenerative diseases. The production of ROS is closely regulated by various proteins, including CBY1, and it is possible that its levels may be elevated in neurodegenerative diseases.

CBY1 as a Potential Drug Target

The potential use of CBY1 as a drug target is based on its involvement in various cellular processes that are critical for the development and progression of neurodegenerative diseases. By targeting CBY1 with small molecules or other therapeutic agents, it is possible to reduce the production of ROS and disrupt the formation of myelin sheath, which could potentially improve the symptoms of neurodegenerative diseases.

One approach to targeting CBY1 is to use small molecules that can inhibit its activity as a protein. Chemicals that are known to inhibit

Protein Name: Chibby Family Member 1, Beta Catenin Antagonist

Functions: Inhibits the Wnt/Wingless pathway by binding to CTNNB1/beta-catenin and inhibiting beta-catenin-mediated transcriptional activation through competition with TCF/LEF transcription factors. Has also been shown to play a role in regulating the intracellular trafficking of polycystin-2/PKD2 and possibly of other intracellular proteins. Promotes adipocyte and cardiomyocyte differentiation

The "CBY1 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 CBY1 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

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