Target Name: EOLA1-DT
NCBI ID: G100131434
Review Report on EOLA1-DT Target / Biomarker Content of Review Report on EOLA1-DT Target / Biomarker
EOLA1-DT
Other Name(s): EOLA1 divergent transcript | LINC00893

EOLA1-DT: A drug Target and Biomarker for the Treatment of Fibrosis

Fibrosis is a chronic and progressive disease that affects various organs and tissues, leading to significant morbidity and mortality. The most common types of fibrosis are caused by repetitive or chronic infections, such as chronic obstructive pulmonary disease (COPD) and chronic kidney disease (CKD), while others are caused by autoimmune diseases, such as rheumatoid arthritis and lupus. The development of fibrosis is a result of an abnormal response of the immune system, which leads to the activation and proliferation of fibroblasts, resulting in the production of extracellular matrix (ECM) components.

EOLA1-DT: A Potential Drug Target and Biomarker

The Extra Cellular Matrix (ECM) is a complex structure that is composed of a variety of cytoskeletal components, including collagen, elasticin, and proteins that are secreted by cells. ECM plays a vital role in cell-to-cell adhesion, tissue repair, and regeneration. Fibroblasts, a type of cell that produces ECM components, are a key player in the production of ECM. The activation and proliferation of fibroblasts are regulated by various factors, including cytokines, growth factors, and mechanical stress.

EOLA1-DT is a protein that is expressed in fibroblasts and is involved in the regulation of fibroblast growth and differentiation. It is a member of the TGF-β family of proteins, which are known for their role in cell proliferation and differentiation. EOLA1-DT has been shown to play a critical role in the regulation of fibroblast growth and the production of ECM components.

EOLA1-DT has been shown to promote the activation and proliferation of fibroblasts, which is a key step in the production of ECM. It has been shown to induce the production of extracellular matrix (ECM) components, such as collagen and elasticin, in fibroblasts. EOLA1-DT has also been shown to regulate the degradation of ECM components, such as collagen, by preventing the activation of enzymes that would cause their breakdown.

EOLA1-DT has also been shown to play a critical role in the regulation of fibroblast differentiation. It has been shown to promote the production of pro-inflammatory cytokines, such as TNF-伪 and IL-6, in fibroblasts, which can stimulate the production of pro-inflammatory cytokines by other immune cells. EOLA1-DT has also been shown to regulate the production of anti-inflammatory cytokines, such as IL-10, in fibroblasts, which can inhibit the production of pro-inflammatory cytokines by immune cells.

EOLA1-DT has also been shown to play a critical role in the regulation of fibroblast-tissue interactions. It has been shown to promote the migration and invasion of fibroblasts into surrounding tissues, which is a key step in the development of fibrosis. EOLA1-DT has also been shown to regulate the production of extracellular matrix (ECM) components in surrounding tissues, which can contribute to the development of ECM in the target tissue.

Drugs that target EOLA1-DT have the potential to treat fibrosis by inhibiting the activity of fibroblasts and ECM components. This could be achieved by inhibiting the signaling pathway that regulates the growth and differentiation of fibroblasts, or by inhibiting the production of ECM components in fibroblasts and surrounding tissues.

Conclusion

EOLA1-DT is a protein that is involved in the regulation of fibroblast growth and differentiation. It has been shown to promote the activation and proliferation of fibroblasts, and to regulate the production of ECM components in fibroblasts and surrounding tissues. The potential drugs that target EOLA1-DT have the

Protein Name: EOLA1 Divergent Transcript

The "EOLA1-DT 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 EOLA1-DT 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

EOLA2 | EOLA2-DT | EOMES | EP300 | EP300-AS1 | EP400 | EP400P1 | EPAS1 | EPB41 | EPB41L1 | EPB41L1-AS1 | EPB41L2 | EPB41L3 | EPB41L4A | EPB41L4A-AS1 | EPB41L4A-DT | EPB41L4B | EPB41L5 | EPB42 | EPC1 | EPC2 | EPCAM | EPCAM-DT | EPDR1 | EPG5 | EPGN | EPHA1 | EPHA1-AS1 | EPHA10 | EPHA2 | EPHA2-AS1 | EPHA3 | EPHA4 | EPHA5 | EPHA5-AS1 | EPHA6 | EPHA7 | EPHA8 | EPHB1 | EPHB2 | EPHB3 | EPHB4 | EPHB6 | Ephrin Receptor | EPHX1 | EPHX2 | EPHX3 | EPHX4 | EPIC1 | EPIST | Epithelial Sodium Channel (ENaC) | EPM2A | EPM2A-DT | EPM2AIP1 | EPN1 | EPN2 | EPN3 | EPO | EPOP | EPOR | Epoxide Hydrolase | EPPIN | EPPK1 | EPRS1 | EPS15 | EPS15L1 | EPS8 | EPS8L1 | EPS8L2 | EPS8L3 | EPSTI1 | EPX | EPYC | EQTN | ER Membrane Protein Complex | ERAL1 | ERAP1 | ERAP2 | ERAS | ERBB2 | ERBB3 | ERBB4 | ERBIN | ERC1 | ERC2 | ERC2-IT1 | ERCC1 | ERCC2 | ERCC3 | ERCC4 | ERCC5 | ERCC6 | ERCC6L | ERCC6L2 | ERCC6L2-AS1 | ERCC8 | EREG | ERF | ERFE | ERG