Target Name: EDA2R
NCBI ID: G60401
Review Report on EDA2R Target / Biomarker Content of Review Report on EDA2R Target / Biomarker
EDA2R
Other Name(s): Tumor necrosis factor receptor superfamily member XEDAR | EDA2R variant 2 | ectodysplasin A2 receptor | EDA-A2 receptor | Tumor necrosis factor receptor superfamily member 27 isoform 1 | EDAA2R | EDA-A2R | X-linked ectodysplasin-A2 receptor | tumor necrosis factor receptor superfamily member XEDAR | TNR27_HUMAN | OTTHUMP00000023449 | Tumor necrosis factor receptor superfamily member 27 | Ectodysplasin A2 receptor, transcript variant 1 | Ectodysplasin A2 receptor, transcript variant 2 | XEDAR | EDA2R variant 1 | X-linked ectodermal dysplasia receptor | TNFRSF27

EDA2R: A Potential Drug Target and Biomarker for Tumor Necrosis Factor Receptor Superfamily Member XEDAR

Abstract:

Tumor necrosis factor receptor superfamily member XEDAR is a protein that plays a crucial role in cell signaling pathways, including cell proliferation and apoptosis. EDA2R, a member of the tumor necrosis factor receptor superfamily, is a potential drug target and biomarker for cancer. This article discusses the biology of XEDAR, its function in cancer progression, and the potential for targeting this protein using small molecules or antibodies.

Introduction:

Tumor necrosis factor receptor superfamily member XEDAR is a protein that is expressed in various tissues and cell types, including epithelial, hematoprotimal, and nervous tissues. XEDAR is involved in cell signaling pathways, including cell proliferation and apoptosis.

EDA2R is a 21-kDa protein that is a member of the tumor necrosis factor receptor superfamily. This protein is expressed in various tissues and cell types, including epithelial, hematoprotimal, and nervous tissues. EDA2R functions as a negative regulator of the TGF-灏? pathway, which is a well-established pathway for cancer development and progression.

In cancer, the TGF-灏? pathway is often hyperactivated, leading to increased cell proliferation and survival. EDA2R functions as a negative regulator of this pathway, promoting cell apoptosis and limiting the negative impact of TGF-灏? on cancer progression.

EDA2R has been identified as a potential drug target and biomarker for cancer. Several studies have shown that inhibiting XEDAR can lead to the inhibition of TGF-灏? signaling, leading to the inhibition of cancer cell proliferation and survival.

Targeting EDA2R:

EDA2R is a protein that can be targeted using various techniques, including small molecules and antibodies. Small molecules can be used to inhibit the activity of EDA2R, while antibodies can be used to selectively target EDA2R and block its function.

One approach to targeting EDA2R is the use of small molecules that inhibit the activity of the TGF-灏? pathway. Small molecules such as inhibitors of the Smad signaling pathway, which is a negative regulator of TGF-灏?, have been shown to be effective in inhibiting the activity of EDA2R.

Another approach to targeting EDA2R is the use of antibodies that specifically recognize and block its function. Monoclonal antibodies (MCAs) have been shown to be effective in targeting EDA2R and inhibiting its function.

Conclusion:

In conclusion, EDA2R is a protein that plays a crucial role in cell signaling pathways, including cell proliferation and apoptosis. As a potential drug target and biomarker for cancer, EDA2R has the potential to be inhibited using various techniques, including small molecules and antibodies. Further research is needed to fully understand the biology of EDA2R and its potential as a drug target and biomarker for cancer.

Protein Name: Ectodysplasin A2 Receptor

Functions: Receptor for EDA isoform A2, but not for EDA isoform A1. Mediates the activation of the NF-kappa-B and JNK pathways. Activation seems to be mediated by binding to TRAF3 and TRAF6

The "EDA2R 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 EDA2R 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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