Target Name: UGT2A2
NCBI ID: G574537
Review Report on UGT2A2 Target / Biomarker Content of Review Report on UGT2A2 Target / Biomarker
UGT2A2
Other Name(s): UDP-glucuronosyltransferase 2A2 | UDPGT 2A2 | UDP glucuronosyltransferase family 2 member A2, transcript variant 1 | UDP glucuronosyltransferase 2 family, polypeptide A2 | UDPGT 2A1 | UDP-glucuronosyltransferase 2A1 | UDP-glucuronosyltransferase 2A2 isoform UGT2A2_i1 | UGT2A1 | UGT2A2 variant 1 | UDP glucuronosyltransferase family 2 member A2

Targeting UGT2A2: Potential Drug Targets and Biomarkers

UGT2A2 (UDP-glucuronosyltransferase 2A2) is a protein that is expressed in various tissues throughout the body, including the liver, pancreas, and gastrointestinal tract. It plays a crucial role in the detoxification of drugs and other harmful substances that are ingested or administered to humans. UGT2A2 is also involved in the metabolism of a variety of drugs, including some statins, which are commonly used to treat high cholesterol.

In recent years, researchers have become increasingly interested in UGT2A2 as a potential drug target or biomarker. This is because the activity of UGT2A2 has been shown to be involved in a wide range of physiological processes, including drug metabolism, inflammation, and cell signaling. As a result, UGT2A2 has become a focus of investigation for researchers looking for new treatments for a variety of diseases.

One of the potential benefits of targeting UGT2A2 is its involvement in drug metabolism. Many drugs work by altering the levels of certain enzymes in the body, and UGT2A2 is known to be involved in this process. For example, UGT2A2 has been shown to play a role in the metabolism of statins, which are commonly used to treat high cholesterol. By inhibiting the activity of UGT2A2, researchers may be able to reduce the amount of statins that are needed to treat cholesterol levels, leading to a more efficient and effective treatment.

Another potential benefit of targeting UGT2A2 is its involvement in inflammation. UGT2A2 has been shown to be involved in the production of pro-inflammatory cytokines, which can contribute to the development of inflammatory diseases. By inhibiting the activity of UGT2A2, researchers may be able to reduce the production of these cytokines and improve the efficacy of treatments for inflammatory diseases.

In addition to its potential role in drug metabolism and inflammation, UGT2A2 is also involved in a variety of other physiological processes that are important for human health. For example, it is involved in the digestion and absorption of nutrients, as well as in the regulation of pH levels in the body.

Despite the potential benefits of targeting UGT2A2, there are also potential drawbacks to this approach. One of the biggest challenges is the potential complexity of the UGT2A2 system, which is still not fully understood. In order to effectively target UGT2A2 and its downstream targets, researchers will need to develop a better understanding of its biology and the interactions between its various components.

Another potential challenge is the potential for unintended consequences when targeting UGT2A2. As with any drug target, there is the risk of targeting unintended proteins that are involved in important physiological processes. Researchers will need to carefully consider these risks and work to minimize them in order to ensure that targeting UGT2A2 does not have negative impacts on other important proteins in the body.

Despite these challenges, the potential benefits of targeting UGT2A2 make it an intriguing target for researchers looking for new treatments for a variety of diseases. By developing new techniques for inhibiting the activity of UGT2A2, researchers may be able to improve the effectiveness of a wide range of treatments and improve the health and well-being of people around the world.

Protein Name: UDP Glucuronosyltransferase Family 2 Member A2

Functions: UDP-glucuronosyltransferase (UGT) that catalyzes phase II biotransformation reactions in which lipophilic substrates are conjugated with glucuronic acid to increase the metabolite's water solubility, thereby facilitating excretion into either the urine or bile (PubMed:19858781, PubMed:18719240, PubMed:23756265, PubMed:23288867). Essential for the elimination and detoxification of drugs, xenobiotics and endogenous compounds (PubMed:19858781, PubMed:23756265). Catalyzes the glucuronidation of endogenous estrogen hormone estradiol (PubMed:18719240, PubMed:23288867). Contributes to bile acid (BA) detoxification by catalyzing the glucuronidation of BA substrates, which are natural detergents for dietary lipids absorption (PubMed:23756265). Shows a potential role in detoxification of toxic waste compounds in the amniotic fluid before birth, and air-born chemical after birth (PubMed:19858781)

The "UGT2A2 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 UGT2A2 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

UGT2A3 | UGT2B10 | UGT2B11 | UGT2B15 | UGT2B17 | UGT2B27P | UGT2B28 | UGT2B29P | UGT2B4 | UGT2B7 | UGT3A1 | UGT3A2 | UGT8 | UHMK1 | UHRF1 | UHRF2 | UICLM | UIMC1 | ULBP1 | ULBP2 | ULBP3 | ULK1 | ULK2 | ULK3 | ULK4 | ULK4P1 | ULK4P2 | ULK4P3 | UMAD1 | UMLILO | UMOD | UMODL1 | UMODL1-AS1 | UMPS | UNC119 | UNC119-myristate complex | UNC119B | UNC13A | UNC13B | UNC13C | UNC13D | UNC45A | UNC45B | UNC50 | UNC5A | UNC5B | UNC5B-AS1 | UNC5C | UNC5CL | UNC5D | UNC79 | UNC80 | UNC93A | UNC93B1 | UNC93B2 | UNC93B3 | UNC93B5 | Uncharactered LOC400863 | Uncharacterized FLJ44790 | Uncharacterized LOC101927121, transcript variant X1 | Uncharacterized LOC101928822, transcript variant X1 | Uncharacterized LOC101929670, transcript variant X1 | Uncharacterized LOC102723888, transcript variant X1 | Uncharacterized LOC102724782, transcript variant X2 | Uncharacterized LOC102724946, transcript variant X3 | Uncharacterized LOC105371833, transcript variant X2 | Uncharacterized LOC105372229, transcript variant X1 | Uncharacterized LOC105373166, transcript variant X2 | Uncharacterized LOC105373806, transcript variant X1 | Uncharacterized LOC105374567, transcript variant X2 | Uncharacterized LOC105374812, transcript variant X2 | Uncharacterized LOC105375163, transcript variant X1 | Uncharacterized LOC105376875, transcript variant X2 | Uncharacterized protein BC001742 | Uncharacterized protein FLJ23867 | Uncharacterized protein MGC16142 | Uncharacterized protein MGC27345 | UNCX | UNG | Uniplex complex | UNK | UNKL | UNQ9370 | UOX | UPB1 | UPF1 | UPF2 | UPF3A | UPF3B | UPK1A | UPK1A-AS1 | UPK1B | UPK2 | UPK3A | UPK3B | UPK3BL1 | UPP1 | UPP2 | UPRT | UQCC1