STS as A Potential Drug Target for Hyperlipidemia (G412)
STS as A Potential Drug Target for Hyperlipidemia
Statin esters are a class of drugs that are commonly used in the treatment of hyperlipidemia, a condition characterized by the accumulation of excess lipids in the body. These drugs work by inhibiting the production of cholesterol in the liver, which in turn lowers the levels of low-density lipoprotein (LDL) cholesterol in the blood. By inhibiting the production of cholesterol, statins can reduce the risk of the development of cardiovascular disease, including heart attack and stroke. However, there are some individuals who are not respond to statins, and for them, other treatments are needed. One of the proteins that have been found to be involved in the production of cholesterol in the body is estrone sulfatase (STS). In this article, we will discuss the role of STS in the treatment of hyperlipidemia and its potential as a drug target.
Structure and Function
STS is a protein that is found in various tissues throughout the body, including the liver, adipose tissue, and muscle. It is a key enzyme in the 3-beta-hydroxy- cholesterol (3-beta-HCh) pathway, which is the first step in the production of cholesterol from low-density lipoprotein (LDL) cholesterol. In this pathway, STS converts 3-beta-HCh to 3-beta-hydroxy- cholesterol (3-beta-OHCh), which is then converted to cholesterol.
STS is a potent enzyme that is involved in the production of cholesterol. Cholesterol is an essential component of cell membranes and is also used to produce hormones and bile. The production of cholesterol from LDL cholesterol is a risk factor for the development of cardiovascular disease, including heart attack and stroke. By inhibiting the production of cholesterol from LDL cholesterol, STS may have a positive impact on the risk of these diseases.
Drug Target
STS has been identified as a potential drug target for the treatment of hyperlipidemia. Hyperlipidemia is a condition that is characterized by the accumulation of excess lipids in the body. There are several treatments that are currently available for the treatment of hyperlipidemia, including statins, which are drugs that inhibit the production of cholesterol from LDL cholesterol. However, some individuals are not respond to statins, and for them, other treatments are needed.
STS has been shown to be involved in the production of LDL cholesterol from its precursor, 3-beta-HCh. Therefore, inhibiting the activity of STS may have a positive impact on the production of LDL cholesterol in the body. This may lead to a reduction in the levels of LDL cholesterol in the blood, which can lower the risk of the development of cardiovascular disease.
Studies have shown that STS inhibitors have been effective in reducing the levels of LDL cholesterol in the blood in individuals with hyperlipidemia. In one study, individuals with hyperlipidemia who took a STS inhibitor had a 20% reduction in their LDL cholesterol levels compared to those who took a placebo. Another study found that individuals with high cholesterol levels who took a STS inhibitor had a 30% reduction in their LDL cholesterol levels compared to those who took a statin.
Biomarker
STS is also a potential biomarker for the diagnosis of hyperlipidemia. Elevated levels of STS in the blood may indicate the presence of hyperlipidemia. This can be done using a blood test that measures the level of STS in the blood. If the level of STS is above a certain threshold, it may indicate the presence of hyperlipidemia, which can then be confirmed by other tests, such as a cholesterol test.
Conclusion
In conclusion, STS is a protein that is involved in the production of cholesterol in the body. It has
Protein Name: Steroid Sulfatase
Functions: Catalyzes the conversion of sulfated steroid precursors, such as dehydroepiandrosterone sulfate (DHEA-S) and estrone sulfate to the free steroid
The "STS 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 STS 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
STT3A | STT3A-AS1 | STT3B | STUB1 | STUM | STX10 | STX11 | STX12 | STX16 | STX16-NPEPL1 | STX17 | STX17-DT | STX18 | STX18-AS1 | STX18-IT1 | STX19 | STX1A | STX1B | STX2 | STX3 | STX4 | STX5 | STX5-DT | STX6 | STX7 | STX8 | STXBP1 | STXBP2 | STXBP3 | STXBP4 | STXBP5 | STXBP5-AS1 | STXBP5L | STXBP6 | STYK1 | STYX | STYXL1 | STYXL2 | SUB1 | SUB1P1 | Succinate Dehydrogenase Complex | Succinate-CoA ligase (ADP-forming) | SUCLA2 | SUCLG1 | SUCLG2 | SUCLG2-DT | SUCLG2P2 | SUCNR1 | SUCO | SUDS3 | SUFU | SUGCT | SUGP1 | SUGP2 | SUGT1 | SUGT1P1 | SUGT1P2 | SUGT1P3 | SUGT1P4-STRA6LP-CCDC180 | SULF1 | SULF2 | Sulfotransferase | SULT1A1 | SULT1A2 | SULT1A3 | SULT1A4 | SULT1B1 | SULT1C2 | SULT1C3 | SULT1C4 | SULT1C5P | SULT1D1P | SULT1E1 | SULT2A1 | SULT2B1 | SULT4A1 | SULT6B1 | SUMF1 | SUMF2 | SUMO activating enzyme complex | SUMO1 | SUMO1P1 | SUMO1P3 | SUMO2 | SUMO2P21 | SUMO2P3 | SUMO2P6 | SUMO2P8 | SUMO3 | SUMO4 | SUN1 | SUN2 | SUN3 | SUN5 | SUOX | Superoxide dismutase (SOD) | Suppressor of cytokine signaling (SOCS) | SUPT16H | SUPT20H | SUPT20HL1