Target Name: TLE4
NCBI ID: G7091
Review Report on TLE4 Target / Biomarker Content of Review Report on TLE4 Target / Biomarker
TLE4
Other Name(s): Groucho-related protein 4 | KIAA1261 | ESG4 | TLE family member 4, transcriptional corepressor, transcript variant 4 | OTTHUMP00000216177 | transducin like enhancer of split 4 | B lymphocyte gene 1 | TLE family member 4, transcriptional corepressor, transcript variant 1 | TLE4_HUMAN | GRG4 | Transducin-like enhancer protein 4 (isoform 4) | Grg-4 | Protein BCE-1 | Transducin-like enhancer protein 4 (isoform 3) | TLE family member 4, transcriptional corepressor, transcript variant 3 | TLE4 variant 3 | Transducin-like enhancer of split 4 (E(sp1) homolog, Drosophila) | transducin-like enhancer of split 4, homolog of Drosophila E(sp1) | TLE4 variant 4 | TLE family member 4, transcriptional corepressor | ESG | BCE-1 | Enhancer of split groucho 4 | Transducin-like enhancer protein 4 (isoform 1) | Transducin-like enhancer protein 4 | BCE1 | E(spl) | enhancer of split groucho 4 | TLE4 variant 1 | Transducin-like enhancer of split 4, homolog of Drosophila E(sp1) | E(spI) | transducin-like enhancer of split 4 (E(sp1) homolog, Drosophila) | groucho-related protein 4

TLE4: A Potential Drug Target and Biomarker for Gout and Other Inflammatory Diseases

Gout is a chronic autoimmune disorder characterized by joint inflammation, pain, and inflammation in the affected joint. It is a leading cause of joint damage and can also have significant morbidity and mortality. The hallmark hallucinosis, gouty arthritis, and joint deformity are some of the most significant clinical manifestations of gout. While there are several medications available for treating gout, the disease remains a significant public health burden due to its chronic nature and limited treatment options.

TLE4, a Groucho-related protein 4, has recently been identified as a potential drug target and biomarker for gout and other inflammatory diseases. In this article, we will discuss the biology of gout, TLE4, and its potential as a drug target.

biology of gout

Gout is a chronic autoimmune disorder that is characterized by the production of immune cells called macrophages in the joints. These macrophages respond to the presence of uric acid crystals, which are a common cause of gout. The macrophages produce a range of pro-inflammatory cytokines, including TNF-伪, IL-1, and IL-6, which attract more immune cells to the affected joint. These cytokines also stimulate the production of other pro-inflammatory cytokines, such as PGE2, which contributes to the production of uric acid crystals.

The hallmark hallucinosis, gouty arthritis, and joint deformity are some of the most significant clinical manifestations of gout. Gouty arthritis is characterized by the presence of pain, erythema, and joint deformity in the affected joint. Erythema is caused by the infiltration of white blood cells, including macrophages, into the affected joint. The production of uric acid crystals by macrophages leads to joint inflammation, pain, and deformity.

TLE4: A Potential Drug Target

TLE4 is a Groucho-related protein 4 that has recently been identified as a potential drug target for gout and other inflammatory diseases. Groucho-related proteins (GRP) are a family of cytoskeletal proteins that play a role in the regulation of cell growth, differentiation, and inflammation. TLE4 is a 14kDa protein that is expressed in various tissues, including skeletal muscles, heart, and brain.

Studies have shown that TLE4 is involved in the regulation of inflammation and immune cell function. TLE4 has been shown to regulate the production of pro-inflammatory cytokines, such as TNF-伪, IL-1, and IL-6, in macrophages. It has also been shown to modulate the production of anti-inflammatory cytokines, such as IL-10, by immune cells.

In addition, TLE4 has been shown to regulate the activity of immune cells, such as T cells and B cells, which play a crucial role in the development of gout. TLE4 has been shown to modulate the production of antibodies by T cells, which may contribute to the development of autoimmune disorders.

TLE4 as a biomarker

TLE4 has also been shown to be a potential biomarker for gout and other inflammatory diseases. The production of uric acid crystals by macrophages is a well-established indicator of gouty arthritis. The production of uric acid crystals by TLE4-expressing macrophages has been shown to be significantly higher than the production of uric acid crystals by TLE4- absence macrophages. This suggests that TLE4 may be a useful biomarker for gout.

In addition, TLE4 has been shown to be involved in the regulation of inflammation and immune cell function. The production of pro-inflammatory cytokines by TLE4-expressing macrophages has been shown to be significantly higher than the production of pro-inflammatory cytokines by TLE4- absence macrophages. This suggests that TLE4 may be a useful biomarker for

Protein Name: TLE Family Member 4, Transcriptional Corepressor

Functions: Transcriptional corepressor that binds to a number of transcription factors. Inhibits the transcriptional activation mediated by PAX5, and by CTNNB1 and TCF family members in Wnt signaling. The effects of full-length TLE family members may be modulated by association with dominant-negative AES. Essential for the transcriptional repressor activity of SIX3 during retina and lens development and for SIX3 transcriptional auto-repression (By similarity)

The "TLE4 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 TLE4 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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