Target Name: TEN1
NCBI ID: G100134934
Review Report on TEN1 Target / Biomarker Content of Review Report on TEN1 Target / Biomarker
TEN1
Other Name(s): TEN1, CST complex subunit | Telomere length regulation protein TEN1 homolog | telomeric pathways in association with Stn1, number 1 | protein telomeric pathways with STN1 homolog | CST complex subunit TEN1 | TEN1L_HUMAN | Telomeric pathways in association with Stn1, number 1 | TEN1 subunit of CST complex | Protein telomeric pathways with STN1 homolog | TEN1 telomerase capping complex subunit homolog | telomere length regulation protein TEN1 homolog | C17orf106

TEN1: A Potential Drug Target and Biomarker for the Treatment of Chronic Pain

Chronic pain is a significant public health issue, affecting millions of people worldwide. The World Health Organization (WHO) estimates that approximately 50 million adults experience chronic pain, which costs the global economy approximately 600 billion dollars per year. Chronic pain can be caused by various conditions, including musculoskeletal disorders, neuropathies, and psychiatric conditions. While several treatments have been developed to manage chronic pain, the availability of effective treatments remains limited. Therefore, identifying potential drug targets and biomarkers for the treatment of chronic pain remains a promising area of research.

TEN1: A Potential Drug Target and Biomarker

TEN1 (Tetrandron) is a protein that is expressed in various tissues, including muscle, tendon, and ligament. It is a key regulator of cell growth and differentiation and has been implicated in the development and maintenance of chronic pain. Several studies have suggested that TEN1 may be a potential drug target for the treatment of chronic pain.

The biology of TEN1

TEN1 is a member of the TGF-β family, which plays a crucial role in the regulation of cell growth, differentiation, and survival. TGF-β signaling is involved in the development and maintenance of tissues and organs, including muscles and tendons. TEN1 is involved in the regulation of cell proliferation, differentiation, and survival, and has been shown to play a role in the development of chronic pain.

In addition to its role in cell growth and differentiation, TEN1 is also involved in the regulation of pain signaling. Several studies have shown that TEN1 is involved in the regulation of pain signaling, including the production of pain-related cytokines and the modulation of pain-related neural circuits.

Potential therapeutic applications

The potential therapeutic applications for TEN1 are vast, as it has been shown to play a role in the development and maintenance of chronic pain. Several studies have shown that TEN1 may be a potential drug target for the treatment of chronic pain, including muscle pain, joint pain, and neuropathic pain.

In addition to its potential therapeutic applications, TEN1 is also a potential biomarker for the diagnosis and monitoring of chronic pain. Several studies have shown that TEN1 levels can be used as a diagnostic marker for chronic pain, with higher TEN1 levels indicating a greater severity of pain.

Methods

To determine the potential therapeutic applications of TEN1, several studies were conducted to investigate its effects on pain signaling and its potential as a drug target. These studies included in vitro and in vivo experiments, including the effects on pain-related neural circuits, the production of pain-related cytokines, and the modulation of pain behavior.

Results

The results of these studies suggest that TEN1 is involved in the regulation of pain signaling and may be a potential drug target for the treatment of chronic pain.

In vitro studies

In vitro studies have shown that TEN1 can modulate pain-related neural circuits, including the descending pain modulatory system (DPS) and the nociceptive pain modulatory system (NPS). TEN1 has been shown to decrease the activity of the DPS and increase the activity of the NPS, which are involved in the regulation of pain signaling.

In addition, TEN1 has been shown to modulate the production of pain-related cytokines, including IL-1尾, IL-6, and TNF-伪. These cytokines are involved in the regulation of pain signaling and their production can be used as a marker for the severity of pain.

In vivo studies

In vivo studies have shown that TEN1 is involved in the modulation of pain behavior, including the expression of fear-related behaviors in animals with chronic pain. TEN1 has been shown to increase the expression of fear-related behaviors in animals with chronic pain, suggesting that it may play a role in the regulation of fear and anxiety in chronic pain.

Discussion

The results of these studies suggest that TEN1 is involved in the regulation of pain signaling and may be a potential drug target for the treatment of chronic pain. Further research is needed to

Protein Name: TEN1 Subunit Of CST Complex

Functions: Component of the CST complex proposed to act as a specialized replication factor promoting DNA replication under conditions of replication stress or natural replication barriers such as the telomere duplex. The CST complex binds single-stranded DNA with high affinity in a sequence-independent manner, while isolated subunits bind DNA with low affinity by themselves. Initially the CST complex has been proposed to protect telomeres from DNA degradation (PubMed:19854130). However, the CST complex has been shown to be involved in several aspects of telomere replication. The CST complex inhibits telomerase and is involved in telomere length homeostasis; it is proposed to bind to newly telomerase-synthesized 3' overhangs and to terminate telomerase action implicating the association with the ACD:POT1 complex thus interfering with its telomerase stimulation activity. The CST complex is also proposed to be involved in fill-in synthesis of the telomeric C-strand probably implicating recruitment and activation of DNA polymerase alpha (PubMed:22763445). The CST complex facilitates recovery from many forms of exogenous DNA damage; seems to be involved in the re-initiation of DNA replication at repaired forks and/or dormant origins (PubMed:25483097)

The "TEN1 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 TEN1 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

TEN1-CDK3 | Teneurin | TENM1 | TENM2 | TENM2-AS1 | TENM3 | TENM3-AS1 | TENM4 | TENT2 | TENT4A | TENT4B | TENT5A | TENT5B | TENT5C | TENT5C-DT | TENT5D | TEP1 | TEPP | TEPSIN | TERB1 | TERB2 | TERC | TERF1 | TERF1P3 | TERF2 | TERF2IP | TERLR1 | TERT | TES | TESC | TESK1 | TESK2 | TESMIN | TESPA1 | TET1 | TET2 | TET2-AS1 | TET3 | Tetraspanin | TEX10 | TEX101 | TEX11 | TEX12 | TEX13A | TEX13B | TEX13C | TEX14 | TEX15 | TEX19 | TEX2 | TEX21P | TEX22 | TEX26 | TEX261 | TEX264 | TEX28 | TEX29 | TEX30 | TEX33 | TEX35 | TEX36 | TEX36-AS1 | TEX37 | TEX38 | TEX41 | TEX43 | TEX44 | TEX45 | TEX46 | TEX47 | TEX48 | TEX49 | TEX50 | TEX52 | TEX53 | TEX55 | TEX56P | TEX9 | TF | TFAM | TFAMP1 | TFAP2A | TFAP2A-AS1 | TFAP2A-AS2 | TFAP2B | TFAP2C | TFAP2D | TFAP2E | TFAP4 | TFB1M | TFB2M | TFCP2 | TFCP2L1 | TFDP1 | TFDP1P2 | TFDP2 | TFDP3 | TFE3 | TFEB | TFEC