Target Name: TOR1AIP2
NCBI ID: G163590
Review Report on TOR1AIP2 Target / Biomarker Content of Review Report on TOR1AIP2 Target / Biomarker
TOR1AIP2
Other Name(s): NET9 | torsin 1A interacting protein 2 | TOR1AIP2 variant 2 | Torsin-1A-interacting protein 2 (isoform b) | 15 kDa interferon-responsive protein | Torsin-1A-interacting protein 2 | TOR1AIP2 variant 3 | interferon responsive gene 15 | torsin-1A-interacting protein 2 | Torsin 1A interacting protein 2, transcript variant 2 | Torsin 1A interacting protein 2, transcript variant 3 | lumenal domain-like LAP1 | TOIP2_HUMAN | torsin A interacting protein 2 | IFRG15 | Lumenal domain-like LAP1 | lumenal domain like LAP1 | LULL1

Introduction to TOR1AIP2, A Potential Drug Target

TOR1AIP2, also known as torsinA-interacting protein 2, is an intriguing molecule that has gained substantial attention in the field of drug discovery and biomarker research. This article aims to provide an in-depth understanding of TOR1AIP2, its role as a potential drug target or biomarker, and its significance in various diseases and conditions.

The Function of TOR1AIP2

TOR1AIP2 is a protein that plays a vital role in cellular processes, particularly in the regulation of protein folding and trafficking. It interacts with torsinA, a member of the AAA+ superfamily, aiding in its proper localization within the endoplasmic reticulum (ER). This proper localization is essential for maintaining ER homeostasis and preventing the accumulation of unfolded or misfolded proteins.

Additionally, TOR1AIP2 has been found to be involved in vesicular trafficking, acting as a regulator of vesicle fusion and transport. It interacts with various proteins involved in vesicle fusion, such as SNAP-25 and syntaxin 1A, to ensure efficient neurotransmitter release and synaptic functioning.

TOR1AIP2 as a Drug Target

Due to its critical role in protein folding and trafficking, TOR1AIP2 has emerged as a potential drug target for several diseases. One of the major areas of interest is neurodegenerative disorders, including Parkinson's disease and dystonia.

Parkinson's disease is characterized by the loss of dopaminergic neurons in the substantia nigra, leading to motor impairments. Research has shown that TOR1AIP2 interacts with torsinA and is implicated in the pathogenesis of Parkinson's disease. Targeting TOR1AIP2 could potentially modulate protein folding and trafficking, leading to neuroprotective effects and slowing down disease progression.

Dystonia is a movement disorder characterized by involuntary muscle contractions, causing twisting and repetitive movements. It has been found that mutations in the TOR1A gene, encoding torsinA, are responsible for a specific form of inherited dystonia, called DYT1 dystonia. TOR1AIP2 interacts with torsinA and may influence its function. Modulating TOR1AIP2 could offer a potential therapeutic strategy for treating dystonia.

Furthermore, TOR1AIP2 has also been implicated in the regulation of immune responses and inflammatory pathways. Dysregulation of these processes is central to autoimmune diseases and chronic inflammation. Targeting TOR1AIP2 could potentially modulate these pathways and provide novel treatment options for such conditions.

TOR1AIP2 as a Biomarker

In addition to its potential as a drug target, TOR1AIP2 has shown promise as a biomarker for various diseases. Biomarkers are measurable indicators that can be used to diagnose diseases, monitor disease progression, or predict treatment responses.

Recent studies have identified altered levels of TOR1AIP2 in different disease states. For instance, increased levels of TOR1AIP2 have been detected in the cerebrospinal fluid of patients with multiple sclerosis (MS). This finding suggests that TOR1AIP2 may serve as a biomarker for MS, potentially aiding in early diagnosis and monitoring disease activity.

Moreover, TOR1AIP2 has been implicated in the development of certain types of cancer. Altered expression of TOR1AIP2 has been observed in breast cancer, ovarian cancer, and hepatocellular carcinoma. Detecting changes in TOR1AIP2 levels may provide valuable insights into cancer progression, prognosis, and treatment response.

Conclusion

TOR1AIP2 is a protein with diverse functions, playing a critical role in protein folding, trafficking, vesicle fusion, and transport. Its involvement in various diseases, including neurodegenerative disorders and cancer, highlights its potential as both a drug target and a biomarker.

Efforts to develop specific inhibitors or modulators of TOR1AIP2 could potentially lead to the discovery of novel therapeutic interventions for Parkinson's disease, dystonia, autoimmune diseases, and certain forms of cancer. Additionally, further research on TOR1AIP2 as a biomarker may improve the diagnosis, prognosis, and monitoring of diseases, aiding in the development of personalized treatments.

Overall, TOR1AIP2 holds great promise in advancing our understanding of diseases and providing new avenues for drug development and precision medicine. Continued research in this field is crucial to unraveling its full potential and translating it into improved healthcare outcomes.

Protein Name: Torsin 1A Interacting Protein 2

Functions: Required for endoplasmic reticulum integrity. Regulates the distribution of TOR1A between the endoplasmic reticulum and the nuclear envelope as well as induces TOR1A, TOR1B and TOR3A ATPase activity

The "TOR1AIP2 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 TOR1AIP2 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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