Target Name: MAGEA1
NCBI ID: G4100
Review Report on MAGEA1 Target / Biomarker Content of Review Report on MAGEA1 Target / Biomarker
MAGEA1
Other Name(s): MAGE-1 antigen | melanoma-associated antigen MZ2-E | melanoma antigen family A, 1 (directs expression of antigen MZ2-E) | MAGE1 | MAGE family member A1 | Melanoma-associated antigen 1 | Cancer/testis antigen 1.1 | cancer/testis antigen 1.1 | melanoma antigen family A1 | melanoma antigen family A 1 | MAGA1_HUMAN | Antigen MZ2-E | cancer/testis antigen family 1, member 1 | melanoma antigen MAGE-1 | MAGE-1 | antigen MZ2-E | CT1.1

MAGEA1: A Protein with Potential as A Drug Target, Biomarker, Or Diagnostic Marker

MAGEA1 (MAGE-1 antigen) is a protein that is expressed in various tissues and cells of the body. It is a member of the MAGE family of proteins, which are known for their ability to induce an immune response. MAGEA1 is primarily expressed in the skin, hair, and nails, and has been shown to play a role in several physiological processes, including immune surveillance and tissue repair.

Recent studies have suggested that MAGEA1 may have potential as a drug target or biomarker. One potential mechanism by which MAGEA1 could be targeted by drugs is through its role in the immune response. MAGEA1 has been shown to be involved in the regulation of T cell responses, and studies have suggested that it may play a role in the development of certain autoimmune diseases. Therefore, drugs that can modulate the activity of T cells or other immune cells may be a potential therapeutic approach for treating autoimmune diseases.

Another potential mechanism by which MAGEA1 could be targeted by drugs is through its role in tissue repair. MAGEA1 has been shown to be involved in the regulation of cell proliferation and differentiation, and has been implicated in the repair of damaged tissue. Therefore, drugs that can promote tissue repair and regeneration may be a potential therapeutic approach for treating injuries or diseases that result in tissue damage.

In addition to its potential as a drug target or biomarker, MAGEA1 has also been shown to have potential as a diagnostic marker. Studies have shown that MAGEA1 is expressed in a variety of tissues and cells, including skin, hair, and nails, and that its expression is often increased in diseases or conditions that are characterized by inflammation or tissue damage. Therefore, MAGEA1 may be a useful diagnostic tool for identifying patients with certain diseases or conditions.

Overall, MAGEA1 is a protein that has significant potential as a drug target or biomarker. Its role in the immune response and tissue repair, as well as its potential as a diagnostic marker, make it an attractive target for drug development in a variety of therapeutic areas. Further research is needed to fully understand the biology and potential therapeutic applications of MAGEA1.

Protein Name: MAGE Family Member A1

Functions: May be involved in transcriptional regulation through interaction with SNW1 and recruiting histone deactelyase HDAC1. May inhibit notch intracellular domain (NICD) transactivation. May play a role in embryonal development and tumor transformation or aspects of tumor progression. Antigen recognized on a melanoma by autologous cytolytic T-lymphocytes

The "MAGEA1 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 MAGEA1 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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