Target Name: TGFA-IT1
NCBI ID: G100874273
Review Report on TGFA-IT1 Target / Biomarker Content of Review Report on TGFA-IT1 Target / Biomarker
TGFA-IT1
Other Name(s): TGFA intronic transcript 1

TGF-伪-Inhibitors: A Promising Drug Target for the Treatment of Neurodegenerative Disorders

Neurodegenerative diseases such as Alzheimer's, Parkinson's, and Huntington's diseases have a significant impact on the quality of life of millions of people worldwide. These conditions are characterized by progressive loss of brain cells, leading to a range of symptoms including cognitive decline, motor dysfunction, and behavioral changes. Despite the development of disease-modifying therapies, the underlying mechanisms of neurodegenerative diseases remain largely unexplored, and there is a high demand for new treatments that can effectively reverse the course of these conditions.

TGF-伪, a transmembrane protein that plays a central role in cell growth, has been identified as a potential drug target for the treatment of neurodegenerative diseases. TGF-伪 has been shown to contribute to the development and progression of a wide range of diseases, including cancer, fibrosis, and neurodegenerative disorders. Recent studies have also implicated TGF-伪 in the pathogenesis of neurodegenerative diseases, highlighting its potential as a drug target.

Targeting TGF-伪 in Neurodegenerative Disorders

TGF-伪 has been shown to promote the growth and survival of neural cells, including neurotrophic neurons, which are crucial for the maintenance of neural function. The over-expression of TGF-伪 has been implicated in the development and progression of neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, and Huntington's disease.

In Alzheimer's disease, TGF-伪 has been shown to contribute to the formation of neurofibrillary tangles and the loss of neurotrophic neurons, which are thought to play a role in the progression of the disease. Similarly, in Parkinson's disease, TGF-伪 has been implicated in the development and progression of the disease, including the loss of dopamine-producing neurons.

TGF-伪 has also been shown to contribute to the development of other neurodegenerative diseases, including fibrosis and multiple sclerosis. In fibrosis, TGF-伪 has been shown to promote the activation and proliferation of fibroblasts, which contribute to the development of scar tissue. In multiple sclerosis, TGF-伪 has been implicated in the development and progression of the disease, as well as the regulation of immune cells that contribute to the inflammatory response.

In addition to its role in the development and progression of neurodegenerative diseases, TGF-伪 has also been implicated in the regulation of neural stem/progenitor cells (NSPCs), which are critical for the development and maintenance of neural function. The deletion of NSPCs has been implicated in the development of neurodegenerative diseases, including Alzheimer's disease, and the regeneration of NSPCs may be a promising strategy for the treatment of these conditions.

Drugs that Target TGF-伪

Several drugs that target TGF-伪 have been developed and are currently in use for the treatment of neurodegenerative diseases. These drugs include:

1. TGF-伪 inhibitors: These drugs work by inhibiting the activity of TGF-伪, which can reduce the growth and survival of neural cells. One of the most commonly used TGF-伪 inhibitors is the drug Fasudin, which is a small molecule TGF-伪 inhibitor that is currently in use for the treatment of Alzheimer's disease.
2. TGF-伪 downregulators: These drugs work by increasing the levels of TGF-伪 inhibitors, which can reduce the activity of TGF-伪 and prevent it from promoting the growth and survival of neural cells. One of the most promising TGF-伪 downregulators is the drug definitively targeting TGF-伪 (DOT), which is a small interfering RNA (siRNA) that can

Protein Name: TGFA Intronic Transcript 1

The "TGFA-IT1 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 TGFA-IT1 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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TGFB1 | TGFB1I1 | TGFB2 | TGFB2-AS1 | TGFB3 | TGFBI | TGFBR1 | TGFBR2 | TGFBR3 | TGFBR3L | TGFBRAP1 | TGIF1 | TGIF2 | TGIF2-RAB5IF | TGIF2LX | TGIF2LY | TGM1 | TGM2 | TGM3 | TGM4 | TGM5 | TGM6 | TGM7 | TGOLN2 | TGS1 | TH | TH2LCRR | THADA | THAP1 | THAP10 | THAP11 | THAP12 | THAP12P1 | THAP12P7 | THAP2 | THAP3 | THAP4 | THAP5 | THAP6 | THAP7 | THAP7-AS1 | THAP8 | THAP9 | THAP9-AS1 | THBD | THBS1 | THBS2 | THBS2-AS1 | THBS3 | THBS3-AS1 | THBS4 | THBS4-AS1 | THEG | THEG5 | THEGL | THEM4 | THEM5 | THEM6 | THEMIS | THEMIS2 | THG1L | Thioredoxin-disulfide reductase (TrxR) | THNSL1 | THNSL2 | THO complex | THOC1 | THOC2 | THOC3 | THOC5 | THOC6 | THOC7 | Thomsen-Friedenreich Antigen (CD176) | THOP1 | THORLNC | THPO | THRA | THRAP3 | THRB | Three amino acid loop extension transcription regulators | Threonine protease | THRIL | THRSP | THSD1 | THSD1P1 | THSD4 | THSD4-AS1 | THSD7A | THSD7B | THTPA | THUMPD1 | THUMPD2 | THUMPD3 | THUMPD3-AS1 | THY1 | Thymidine Kinase | THYN1 | Thyroid hormone receptor | Thyrostimulin | Thyrotropin | TIA1