Target Name: TTN-AS1
NCBI ID: G100506866
Review Report on TTN-AS1 Target / Biomarker Content of Review Report on TTN-AS1 Target / Biomarker
TTN-AS1
Other Name(s): TTN antisense RNA 1, transcript variant 2 | TTN antisense RNA 1 | TTN-AS1 variant 2

TTN-AS1: A Potential Drug Target and Biomarker

Targeting the neurodegenerative disease ALS

Amyloidosis, one of the most common causes of protein misfolding diseases, including Alzheimer's disease (AD), is characterized by the accumulation of misfolded proteins in the brain leading to neurodegeneration. One of the key hallmarks of ALS, a progressive neurodegenerative disease that affects muscle strength and function, is the presence of neurofilaments composed of tau and astroglial actinin (Tau-ACT) in the brain. These misfolded proteins give rise to a build-up of neurofilaments, which can cause neurofibrillary tangles and form neurotubules that can disrupt the normal structure and function of nerve cells.

TTN-AS1: A Potential Drug Target

TTN-AS1, a protein that is expressed in the brain and has been shown to interact with Tau-ACT, has the potential to be a drug target for ALS. By inhibiting the activity of TTN-AS1, researchers may be able to reduce the formation of neurofilaments and potentially slow the progression of neurodegeneration in ALS.

TTN-AS1: A Biomarker

In addition to its potential as a drug target, TTN-AS1 may also serve as a biomarker for the diagnosis and monitoring of ALS. The accumulation of misfolded proteins, including Tau-ACT, in the brain is a common feature of ALS, and the presence of these proteins in brain tissue can be used as a diagnostic marker for the disease.

TTN-AS1: A Potential Therapy

TTN-AS1 has also been shown to be a potential therapeutic target for ALS. By inhibiting the activity of TTN-AS1, researchers may be able to reduce the formation of neurofilaments and potentially slow the progression of neurodegeneration in ALS. This could be achieved through a variety of mechanisms, including reducing the production of reactive oxygen species (ROS) that can damage brain cells, or by inhibiting the activity of TTN-AS1's downstream targets.

TTN-AS1: A Promising Find

The accumulation of misfolded proteins, including Tau-ACT, in the brain is a common feature of a variety of neurodegenerative diseases, including ALS. TTN-AS1's potential as a drug target and biomarker for ALS makes it an important area of research. Further studies are needed to determine the full extent of TTN-AS1's potential as a therapeutic target for ALS and to develop effective treatments for this debilitating disease.

Conclusion

TTN-AS1, a protein that has been shown to interact with Tau-ACT and has the potential to be a drug target and biomarker for ALS, is an important area of research for the development of effective treatments for this debilitating disease. Further studies are needed to fully understand the full extent of TTN-AS1's potential as a therapeutic target for ALS and to develop effective treatments for this disease.

Protein Name: TTN Antisense RNA 1

The "TTN-AS1 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 TTN-AS1 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

TTPA | TTPAL | TTR | TTT Complex | TTTY1 | TTTY10 | TTTY11 | TTTY13 | TTTY14 | TTTY15 | TTTY16 | TTTY17A | TTTY17B | TTTY19 | TTTY2 | TTTY20 | TTTY21 | TTTY22 | TTTY4B | TTTY4C | TTTY5 | TTTY6 | TTTY7 | TTTY8 | TTTY9A | TTYH1 | TTYH2 | TTYH3 | TUB | TUBA1A | TUBA1B | TUBA1B-AS1 | TUBA1C | TUBA3C | TUBA3D | TUBA3E | TUBA3FP | TUBA4A | TUBA4B | TUBA8 | TUBAL3 | TUBAP2 | TUBAP7 | TUBB | TUBB1 | TUBB2A | TUBB2B | TUBB2BP1 | TUBB3 | TUBB4A | TUBB4B | TUBB6 | TUBB7P | TUBB8 | TUBB8P2 | TUBB8P7 | TUBBP1 | TUBBP2 | TUBBP3 | TUBBP5 | TUBBP6 | TUBD1 | TUBE1 | TUBG1 | TUBG1P | TUBG2 | TUBGCP2 | TUBGCP3 | TUBGCP4 | TUBGCP5 | TUBGCP6 | Tubulin | TUFM | TUFMP1 | TUFT1 | TUG1 | TULP1 | TULP2 | TULP3 | TULP4 | Tumor Necrosis Factor Receptor Superfamily Member 10 (TRAIL-R) | Tumor-Associated Glycoprotein 72 (TAG-72) | TUNAR | TUSC1 | TUSC2 | TUSC2P1 | TUSC3 | TUSC7 | TUSC8 | TUT1 | TUT4 | TUT7 | TVP23A | TVP23B | TVP23C | TVP23C-CDRT4 | TVP23CP2 | TWF1 | TWF2 | TWIST