Target Name: THSD7B
NCBI ID: G80731
Review Report on THSD7B Target / Biomarker Content of Review Report on THSD7B Target / Biomarker
THSD7B
Other Name(s): Thrombospondin, type I, domain containing 7B | thrombospondin, type I, domain containing 7B | KIAA1679 | thrombospondin type 1 domain containing 7B | OTTHUMP00000204182 | Thrombospondin type-1 domain-containing protein 7B | THS7B_HUMAN

THSD7B: A Potential Drug Target and Biomarker

Thrombospondin (TSP) is a protein that plays a critical role in the regulation of blood clotting. It is a large glycoprotein that is expressed in various tissues and cells, including endothelial cells, smooth muscle cells, and platelet cells. TSP is composed of a variable region (V1) and a variable fragment (V2), which contain distinct functions. The V1 region contains a N-terminal domain that is responsible for TSP's ability to interact with heparin and thrombin, while the V2 region contains a C-terminal domain that is involved in TSP's aggregation and clotting properties.

TSP has been implicated in the development and progression of various cardiovascular diseases, including thromboembolic stroke, deep vein thrombosis, and acute myocardial infarction. It is also associated with an increased risk of bleeding complications, such as intracranial hemorrhage and mobile Internet thrombosis. Given its significant impact on cardiovascular health, targeting TSP is a promising strategy for the development of new treatments for these diseases.

One potential drug target for TSP is the inhibition of its aggregation and clotting properties. Several studies have shown that TSP can form aggregates in various conditions, including thrombosis and blood clots. The aggregation of TSP is regulated by various factors, including shear stress, temperature , and pH. By inhibiting TSP aggregation, researchers hope to reduce the risk of cardiovascular events associated with TSP exposure.

Another potential drug target for TSP is its role in platelet function. TSP has been shown to regulate platelet aggregation and influence platelet function. It has been shown to increase platelet aggregation in response to various stimuli, including thrombin and collagen. By inhibiting TSP effects on platelet function, researchers hope to develop new treatments for thromboembolic stroke and other cardiovascular diseases.

In addition to its potential drug targets, TSP is also a potential biomarker for cardiovascular disease. The aggregation of TSP is a well-established biomarker for the presence of TSP in patient samples, including blood clots and thrombus. The concentration of TSP in blood samples can also be used as a predictor of cardiovascular disease risk.

Given its potential impact on cardiovascular health, targeting TSP is a promising strategy for the development of new treatments for thromboembolic stroke and other cardiovascular diseases. Researchers are currently working to develop new TSP inhibitors for clinical trials. These studies will help determine the safety and effectiveness of these new treatments, as well as provide insights into the underlying mechanisms that regulate TSP aggregation and clotting.

In conclusion, THSD7B (Thrombospondin, type I, domain containing 7B) is a protein that plays a critical role in the regulation of blood clotting. Its aggregation and clotting properties are associated with the development and progression of various cardiovascular diseases. Targeting TSP is a promising strategy for the development of new treatments for thromboembolic stroke and other cardiovascular diseases. Further research is needed to determine the safety and effectiveness of new TSP inhibitors and to understand the underlying mechanisms that regulate TSP aggregation and clotting.

Protein Name: Thrombospondin Type 1 Domain Containing 7B

The "THSD7B 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 THSD7B 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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