Target Name: THBD
NCBI ID: G7056
Review Report on THBD Target / Biomarker Content of Review Report on THBD Target / Biomarker
THBD
Other Name(s): Fetomodulin | BDCA3 | TRBM_HUMAN | THRM | sTM_(HUMAN) | CD141 antigen | Thrombomodulin | TM | soluble thrombomodulin | thrombomodulin | BDCA-3 | AHUS6 | fetomodulin | THPH12 | CD141

Introduction to THBD
THBD (Thrombomodulin) is a glycoprotein that plays a pivotal role in maintaining hemostasis, inflammation, and endothelial cell functions. It is primarily expressed on the surface of endothelial cells lining the blood vessels. THBD acts as a drug target as well as a biomarker for various clinical conditions. This article aims to delve deeper into the significance of THBD as a drug target and biomarker, exploring its various roles and potential clinical applications.

The Role of THBD as a Drug Target:
THBD has gained considerable attention as a potential drug target due to its involvement in several pathological processes. One of its crucial roles is in coagulation regulation. THBD binds to thrombin, a key enzyme in blood clot formation, forming the thrombin-thrombomodulin complex. This complex activates protein C, inhibiting the coagulation cascade and preventing excessive clot formation. Dysfunction of THBD can lead to aberrant coagulation, predisposing individuals to thrombotic disorders such as deep vein thrombosis and pulmonary embolism.

Targeting THBD's interaction with thrombin has shown promising therapeutic potential. Researchers have developed novel drugs that mimic the action of thrombomodulin, enhancing its ability to activate protein C and mediate anticoagulation. These drugs offer new therapeutic opportunities for patients with thrombotic disorders by directly modulating THBD's function.

Another important aspect of THBD as a drug target lies in its involvement in inflammatory processes. THBD promotes the formation of activated protein C (APC), which possesses anticoagulant and anti-inflammatory properties. APC inhibits the expression of pro-inflammatory molecules and exerts cytoprotective effects on endothelial cells, suppressing inflammation within blood vessels. Modulating THBD's interaction with thrombin can help regulate APC generation, presenting novel approaches for managing inflammatory diseases, such as sepsis and rheumatoid arthritis.

THBD as a Biomarker:
THBD has also emerged as a valuable biomarker in various clinical settings due to its close association with endothelial cell dysfunction and damage. Endothelial dysfunction is a hallmark of several vascular conditions, including atherosclerosis, hypertension, and diabetes. As THBD is predominantly expressed on endothelial cells, its levels in circulation can serve as an indicator of endothelial cell health.

Elevated levels of soluble THBD (sTHBD) in the blood have been observed in patients with endothelial dysfunction, making it a potential biomarker for monitoring and predicting vascular complications. Numerous studies have demonstrated a correlation between elevated sTHBD levels and increased risk of cardiovascular events, providing insights into early detection and risk stratification of patients.

Moreover, monitoring THBD levels during cancer progression has shown promise. Malignant tumors often promote the activation of coagulation pathways and disrupt the delicate balance between pro-coagulant and anticoagulant factors. As THBD is a key regulator of hemostasis, alterations in its expression or release into the bloodstream have been reported in various cancers. These changes reflect the tumor's impact on the vascular system, suggesting the potential of THBD as a prognostic and predictive biomarker in oncology.

Potential Clinical Applications:
The significance of THBD as a drug target and biomarker opens up a multitude of clinical applications. Targeting THBD's interaction with thrombin has the potential to revolutionize anticoagulant therapy, providing safer and more personalized treatment options for patients with thrombotic disorders. By directly enhancing THBD's activation of protein C, future drugs could minimize the risk of bleeding complications associated with traditional anticoagulants while maintaining antithrombotic effects.

Additionally, the measurement of sTHBD levels could aid in the early detection and prevention of vascular complications. Routine assessment of THBD levels in high-risk individuals may enable timely intervention and preventative measures, reducing the incidence of cardiovascular events and improving patient outcomes.

In the oncology field, utilizing THBD as a biomarker could enhance cancer diagnosis, prognosis, and treatment response assessment. Monitoring dynamic changes in THBD levels throughout the disease course might facilitate the early detection of metastasis or therapeutic resistance, guiding personalized treatment decisions.

Conclusion:
THBD holds immense potential as both a drug target and biomarker. Understanding its roles in coagulation regulation, inflammation, and endothelial dysfunction paves the way for the development of novel therapies and diagnostic strategies. Exploiting THBD's interactions with thrombin and measuring its levels in circulation offers new avenues for managing thrombotic disorders, inflammatory diseases, and various malignancies. The continued exploration of THBD's intricacies promises advancements in precision medicine, leading to improved patient outcomes and better-tailored therapeutic interventions.

Protein Name: Thrombomodulin

Functions: Thrombomodulin is a specific endothelial cell receptor that forms a 1:1 stoichiometric complex with thrombin. This complex is responsible for the conversion of protein C to the activated protein C (protein Ca). Once evolved, protein Ca scissions the activated cofactors of the coagulation mechanism, factor Va and factor VIIIa, and thereby reduces the amount of thrombin generated

The "THBD 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 THBD 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

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 | TIAF1 | TIAL1 | TIAM1 | TIAM1-AS1 | TIAM2 | TICAM1 | TICAM2 | TICAM2-AS1 | TICRR | Tie Receptor | TIE1 | TIFA | TIFAB | TIGAR | TIGD1 | TIGD2 | TIGD3 | TIGD4 | TIGD5 | TIGD6 | TIGD7 | TIGIT | TIM22 complex | TIM23 Complex | TIMD4 | TIMELESS | TIMM10 | TIMM10B | TIMM13 | TIMM17A | TIMM17B | TIMM21 | TIMM22 | TIMM23 | TIMM29 | TIMM44 | TIMM50 | TIMM8-TIMM13 complex | TIMM8A | TIMM8AP1 | TIMM8B | TIMM9 | TIMMDC1 | TIMP1 | TIMP2